Histochemical and cytochemical methods for detecting NTRK fusion proteins

Abstract

To provide materials and methods for detecting NTRK rearrangements via affinity staining.SOLUTION: Samples are stained with a biomarker-specific reagent (such as an antibody) that binds to a retained portion of TrkA, TrkB, and / or TrkC. A staining pattern is evaluated, and presence of a Trk fusion is determined by detecting whether or not the sample has at least a threshold number of cells having a threshold staining intensity. In some cases, the same scoring methodology is applied regardless of a staining localization pattern. In other cases, a cytoplasmic and / or membranous localization is scored by a first methodology, whereas a nuclear localization is scored by a second methodology. The methods disclosed herein may be applied across non-endocrine solid tumor types.SELECTED DRAWING: None

Description

[Technical Field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Patent Application No. 62 / 731,032, filed September 13, 2018, entitled "Histochemical and Cytochemical Methods for Detecting NTRK Fusion Proteins," the contents of which are incorporated herein by reference in their entirety.

[0002] Incorporation by Reference of Sequence Listing This application incorporates by reference the sequence listing submitted herewith in computer readable form with file name "P35023-WO PCT fling sequence listing" (21,260 bytes), created on September 9, 2019.

[0003] The present disclosure relates, inter alia, to methods for the histochemical and cytochemical detection of fusion proteins involving NTRK gene products, materials, kits, and systems useful in such methods, and products resulting from the practice of such methods. [Background technology]

[0004] Neurotrophic tyrosine receptor kinases (NTRK1, NTRK2, and NTRK3) are a family of genes encoding receptor tyrosine kinase proteins (TRKA, TRKB, and TRKC) that play a role in the development and maturation of the central and peripheral nervous systems (Barbacid I, Barbacid II, Lemmon & Schlessinger, and Klein). In cancer, the intact kinase domain of one of the three NTRK genes can be fused to various upstream partners (e.g., ETV6, LMNA, and TPM3), replacing the ligand-binding domain of the TRK protein with a structural motif that promotes dimerization (Eide, Luberg, & Vaishnavi). This results in constitutive activation of TRK signaling and uncontrolled proliferation due to expression of the fusion protein.

[0005] NTRK gene fusions are characteristic of certain rare tumors, such as infantile fibrosarcoma, congenital mesoblastic nephroma, secretory breast cancer, and secretory carcinoma of the salivary glands (MASC) (Argani, Bishop, Bourgeois, Rubin, & Tognon). Conversely, NTRK gene fusions rarely occur in adult and pediatric solid tumors, including, but not limited to, appendix cancer, breast cancer, cholangiocarcinoma, colorectal cancer (CRC), GIST, lung cancer, melanoma, pancreatic cancer, thyroid cancer, and various sarcomas (DeBraud, Brzezianska, Fernandez-Cuesta, Leeman-Neill, & Ross). Identifying NTRK gene fusions is clinically important because small molecule inhibitors are currently in development for the treatment of solid tumors with NTRK gene fusions (Vaishnavi & De Braud).

[0006] To date, there is no gold standard for detecting NTRK fusions in tumors due to inconsistent specificity and sensitivity across different methodologies. Current detection methods include fluorescence in situ hybridization (FISH), in situ hybridization (ISH), next-generation sequencing (NGS), and immunohistochemistry (IHC). Optimization and enumeration / interpretation of FISH and ISH assays can be challenging. NGS is highly specific but lacks sensitivity. In contrast, IHC can be highly sensitive but detects protein expression rather than the actual presence of the fusion. Additionally, the endogenous presence of wild-type TRK protein in some tumors (i.e., neuroendocrine tumors and GISTs) can make optimizing IHC assays for fusion products, and subsequently, developing specific scoring algorithms to select for these fusion products, challenging. Summary of the Invention

[0007] The present disclosure relates to methods for identifying non-neuroendocrine tumors driven by TRK fusion proteins.

[0008] In one embodiment, a method of detecting a TrkA, TrkB, or TrkC fusion protein in a non-neuroendocrine tumor sample is provided, the method comprising: affinity histochemically staining the sample with a biomarker-specific reagent that specifically binds to one or more of: an amino acid sequence comprising, consisting essentially of, or consisting of residues 363-760 of SEQ ID NO:1; an amino acid sequence comprising, consisting essentially of, or consisting of residues 646-838 of SEQ ID NO:2; or an amino acid sequence comprising, consisting essentially of, or consisting of residues 718-839 of SEQ ID NO:3; detecting a staining pattern in the sample; and scoring the sample as positive for a fusion protein involving TrkA, TrkB, or TrkC if the sample has a cytoplasmic and / or membranous staining pattern and has equal to or greater than a first threshold percentage of tumor cells that stain above a predetermined specific staining intensity, or if the sample has a nuclear staining pattern and equal to or greater than a second threshold percentage of cells within a threshold tumor cell area that specifically stain at any intensity.

[0009] In one embodiment, a method is provided for detecting a TrkA, TrkB, or TrkC fusion protein in a non-neuroendocrine tumor sample, the method comprising: affinity histochemically staining the sample with a biomarker-specific reagent that specifically binds to an amino acid sequence comprising, consisting essentially of, or consisting of residues 363-760 of SEQ ID NO:1; an amino acid sequence comprising, consisting essentially of, or consisting of residues 646-838 of SEQ ID NO:2; and an amino acid sequence comprising, consisting essentially of, or consisting of residues 718-839 of SEQ ID NO:3; detecting a staining pattern in the sample; and scoring the sample as positive for a fusion protein involving TrkA, TrkB, or TrkC if the sample has a cytoplasmic and / or membranous staining pattern and has equal to or greater than a first threshold percentage of tumor cells that stain above a predetermined specific staining intensity, or if the sample has a nuclear staining pattern and equal to or greater than a second threshold percentage of cells within a threshold tumor cell area that specifically stain at any intensity.

[0010] In one embodiment, a method is provided for detecting a TrkA, TrkB, or TrkC fusion protein in a non-neuroendocrine tumor sample, the method comprising affinity histochemically staining the sample with a biomarker-specific reagent that specifically binds to an amino acid sequence consisting of amino acids 816-838 of SEQ ID NO:2; detecting a staining pattern in the sample; and scoring the sample as positive for a fusion protein involving TrkA, TrkB, or TrkC if the sample has a cytoplasmic and / or membranous staining pattern and has equal to or greater than a first threshold percentage of tumor cells that stain above a predetermined specific staining intensity, or if the sample has a nuclear staining pattern and equal to or greater than a second threshold percentage of cells within a threshold tumor cell area that specifically stain at any intensity.

[0011] In one embodiment, a method of detecting an NTRK rearrangement in a non-neuroendocrine tumor sample is provided, the method comprising detecting the presence of a Trk fusion protein in the sample according to the methods described herein, and if the sample scores positive for a fusion protein involving TrkA, TrkB, or TrkC, confirming the presence of an NTRK rearrangement by screening the sample by sequencing, reverse transcription polymerase chain reaction, or in situ hybridization.

[0012] In one embodiment, a method of selecting a patient to receive a Trk-directed therapy is provided, the method comprising detecting the presence of a Trk fusion protein or an NTRK rearrangement in a non-neuroendocrine tumor sample according to the methods described herein, and selecting the patient to receive the therapy if the sample scores as positive for a fusion protein involving TrkA, TrkB, or TrkC, or if an NTRK rearrangement is detected.

[0013] Also provided in one embodiment is a method of staining a sample for the presence or absence of TrkA, TrkB, or TrkC, and fusion proteins comprising their kinase domains, comprising: (a) subjecting the sample to a heat-induced epitope retrieval process; and (b) contacting the sample with a set of biomarker-specific reagents and detection reagents to deposit a brightfield dye near any biomarker-specific reagents bound to the sample, wherein the biomarker-specific reagents specifically bind to one or more of an amino acid sequence comprising, consisting essentially of, or consisting of residues 363-760 of SEQ ID NO:1; an amino acid sequence comprising, consisting essentially of, or consisting of residues 646-838 of SEQ ID NO:2; or an amino acid sequence comprising, consisting essentially of, or consisting of residues 718-839 of SEQ ID NO:3.

[0014] In one embodiment, a method of staining a sample for the presence or absence of TrkA, TrkB, or TrkC, and fusion proteins comprising their kinase domains, is also provided, the method comprising: (a) subjecting the sample to a heat-induced epitope retrieval process; and (b) contacting the sample with a set of biomarker-specific and detection reagents to deposit a brightfield dye near any biomarker-specific reagents bound to the sample, wherein the biomarker-specific reagent is a primary antibody that specifically binds to one or more of: an amino acid sequence comprising, consisting essentially of, or consisting of residues 363-760 of SEQ ID NO:1; an amino acid sequence comprising, consisting essentially of, or consisting of residues 646-838 of SEQ ID NO:2; or an amino acid sequence comprising, consisting essentially of, or consisting of residues 718-839 of SEQ ID NO:3; and the set of detection reagents comprises a secondary antibody immunoreactive with the primary antibody, a tertiary antibody immunoreactive with the secondary antibody conjugated to an enzyme, and a set of reagents reactive with an enzyme that result in the deposition of the brightfield dye in the sample.

[0015] In one embodiment, a method of staining a sample for the presence or absence of TrkA, TrkB, or TrkC, and fusion proteins comprising their kinase domains, is also provided, the method comprising: (a) subjecting the sample to a heat-induced epitope retrieval process; and (b) contacting the sample with a set of biomarker-specific and detection reagents to deposit a brightfield dye near any biomarker-specific reagents bound to the sample, wherein the biomarker-specific reagent is a primary antibody that specifically binds to each of: an amino acid sequence comprising, consisting essentially of, or consisting of residues 363-760 of SEQ ID NO:1; an amino acid sequence comprising, consisting essentially of, or consisting of residues 646-838 of SEQ ID NO:2; or an amino acid sequence comprising, consisting essentially of, or consisting of residues 718-839 of SEQ ID NO:3; and the set of detection reagents comprises a secondary antibody immunoreactive with the primary antibody, a secondary antibody immunoreactive with an enzyme-conjugated tertiary antibody, and a set of enzyme-reactive reagents that result in deposition of the brightfield dye in the sample.

[0016] Other embodiments will become apparent from the following disclosure. [Brief explanation of the drawings]

[0017] [Figure 1] Sequence alignment between exemplary conserved portions of TrkA (amino acid residues 363-760 of SEQ ID NO: 1), TrkB (amino acid residues 646-838 of SEQ ID NO: 2), and TrkC (amino acid residues 718-839 of SEQ ID NO: 3). Sequence alignments were generated using the Kalign Multiple Sequence Alignment tool by EMBL-EBI (https: / / www.ebi.ac.uk / Tools / msa / kalign / ). Default settings were used, including the ClustalW output format, a gap open penalty of 11, a gap extension penalty of 0.85, a terminal gap penalty of 0.45, and a bonus score of 0. [Figure 2A]IHC Results for Trk Fusions in Multiple Tumor Types Orthogonal testing methods were used to assess the presence of Trk fusions. [Figure 2B] IHC results in Trk fusions in multiple tumor types. Orthogonal testing was used to assess the absence of Trk fusions. [Figure 3A] Staining distribution of tumor types for ISH-confirmed fusion-positive cases in the dataset by tumor cell staining percentage (0-100%) and staining intensity (0-3+). Circles represent fusion-negative cases, and triangles represent fusion-positive cases. Diamonds indicate cases where fusion was detected by ISH but a fixed gradient was observed. Patterns represent various tumor histologies. Figure 5a and Figure 5b show the staining distribution of neuroendocrine tumors in which no fusion-positive cases were detected. [Figure 3B] Staining distribution of tumor types for ISH-confirmed fusion-negative cases in the dataset by percentage of tumor cell staining (0–100%) and intensity of staining (0–3+). [Figure 4] Subcategorization of solid tumors based on IHC and ISH testing. [Figure 5] Examples of differences in staining pattern localization obtained with the staining methods described herein. (A) Cytoplasmic / membrane staining pattern in a colorectal tumor determined to have an NTRK1 rearrangement by break-apart in situ hybridization assay and confirmed to have an NTRK1-TPM3 fusion by next-generation sequencing. (B) Cytoplasmic staining pattern in a colorectal tumor determined to have an NTRK1 rearrangement by break-apart in situ hybridization assay and confirmed to have an NTRK1-EML4 fusion by next-generation sequencing. (C) Nuclear / cytoplasmic staining pattern in a mammary analogue secretory carcinoma (MASC) determined to have an NTRK3 rearrangement by break-apart in situ hybridization assay and confirmed to have an NTRK3-ETV6 fusion by next-generation sequencing. [Figure 6]Examples of fixed gradients within tissues, and a demonstration that nuclear localization appears to be more affected by the gradient than cytoplasmic / membrane localization. The bottom row shows low magnification, and the top row shows high magnification of a subsection of the image immediately below. DETAILED DESCRIPTION OF THE INVENTION

[0018] I. Definition Unless otherwise defined, technical and scientific terms used herein have the same meaning as commonly understood by those skilled in the art.See, for example, Lackie, DICTIONARY OF CELL AND MOLECULAR BIOLOGY, Elsevier (4th ed. 2007); Sambrook et al., MOLECULAR CLONING, A LABORATORY MANUAL, Cold Springs Harbor Press (Cold Springs Harbor, NY 1989). The term "a" or "an" is intended to mean "one or more." The terms "comprise," "comprises," and "comprising," when preceding a list of steps or elements, are intended to mean that the addition of additional steps or elements is optional and not excluded.

[0019] Antibody: The term "antibody" is used herein in the broadest sense and encompasses a variety of antibody structures, including, but not limited to, monoclonal antibodies, polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies), and antibody fragments, so long as they exhibit the desired antigen-binding activity.

[0020] Antibody fragment: An "antibody fragment" refers to a molecule other than an intact antibody that contains a portion of the intact antibody that binds the antigen to which the intact antibody binds. Examples of antibody fragments include, but are not limited to, Fv, Fab, Fab', Fab'-SH, F(ab')2, diabodies, linear antibodies, single-chain antibody molecules (e.g., scFv), and multispecific antibodies formed from antibody fragments.

[0021] Biomarker: As used herein, the term "biomarker" refers to any molecule or group of molecules found in a biological sample that can be used to characterize the biological sample or the subject from which the biological sample is obtained. For example, a biomarker can be a molecule or group of molecules whose presence, absence, or relative abundance is: · characteristics of particular cell or tissue types or conditions; Characteristics of a particular medical condition or situation; or · An indication of the severity of a pathological condition, the likelihood of progression or regression of a pathological condition, and / or the likelihood that a pathological condition will respond to a particular treatment.

[0022] As another example, a biomarker can be a cell type or a microorganism (bacteria, mycobacteria, fungi, viruses, etc.), or a substitute molecule or group of molecules thereof.

[0023] Biomarker-specific reagent: A specific detection reagent, such as a primary antibody, that can bind directly and specifically to one or more biomarkers in a cell sample.

[0024] Cell sample: As used herein, the term "cell sample" refers to any sample containing intact cells, such as a cell culture, a body fluid sample, or a surgical specimen taken for pathological, histological, or cytological interpretation.

[0025] Cytochemical detection: A process involving labeling biomarkers or other structures in a cytological sample with biomarker-specific and detection reagents in a manner that allows microscopic detection of the biomarker or other structures in the context of intact cells.

[0026] Cytological sample: As used herein, the term "cytological sample" refers to a cell sample that does not have cross-sectional spatial relationships in vivo (such as cell samples derived from blood samples, urine samples, sputum, etc.) or in which the cross-sectional spatial relationships are at least partially destroyed (such as tissue smears, liquid-based cytology samples, fine needle aspirates, etc.).

[0027] Detection Reagent: A "detection reagent" is any reagent used to deposit a stain near a biomarker-specific reagent in a cell sample. Non-limiting examples include a biomarker-specific reagent (such as a primary antibody), a secondary detection reagent (such as a secondary antibody that can bind to a primary antibody), a tertiary detection reagent (such as a tertiary antibody that can bind to a secondary antibody), an enzyme directly or indirectly associated with a biomarker-specific reagent, chemicals reactive with such enzymes that result in the deposition of a fluorescent or chromogenic stain, wash reagents used between staining steps, etc.

[0028] Detectable moiety: A molecule or material capable of producing a detectable signal (visual, electronic, etc., or otherwise) that indicates the presence (i.e., qualitative analysis) and / or concentration (i.e., quantitative analysis) of a detectable moiety deposited on a sample. The detectable signal can be produced by any known or yet to be discovered mechanism, including absorption, emission, and / or scattering of photons (including photons at radio, microwave, infrared, visible, and ultraviolet frequencies). The term "detectable moiety" includes chromogenic, fluorescent, phosphorescent, and luminescent molecules and materials, as well as catalysts (such as enzymes) that convert one substance to another to provide a detectable difference (by converting a colorless substance to a colored substance or vice versa, or by producing a precipitate or increasing the turbidity of the sample). In some examples, the detectable moiety is a fluorophore, belonging to several general chemical classes, including coumarins, fluoresceins (or fluorescein derivatives and analogs), rhodamines, resorufins, luminophores, and cyanines. Additional examples of fluorescent molecules are described in "Molecular Probes Handbook - A Guide to Fluorescent Probes and Labeling Technologies," Molecular Probes, Eugene, OR, ThermoFisher Scientific, 11th Edition. In other embodiments, the detectable moiety is diaminobenzidine (DAB), 4-(dimethylamino)azobenzene-4'-sulfonamide (DABSYL), tetramethylrhodamine (DISCOVERY Purple), N,N'-biscarboxypentyl-5,5'-disulfonato-indo-dicarbocyanine (Cy5), and rhodamine 110 (rhodamine).

[0029] Histochemical detection: A process involving labeling a biomarker or other structure in a tissue sample with a biomarker-specific reagent and a detection reagent in a manner that allows for microscopic detection of the biomarker or other structure in relation to the cross-sectional relationships between the structures in the tissue sample.

[0030] Monoclonal antibody: An antibody obtained from a population of substantially homogeneous antibodies, i.e., antibodies in which the individual antibodies comprising the population are identical and / or bind the same epitope, except for variant antibodies that contain naturally occurring mutations or that may arise during the manufacture of a monoclonal antibody preparation, in which such variants are generally present in minor amounts. In contrast to polyclonal antibody preparations, which typically include different antibodies directed against different determinants (epitopes), each monoclonal antibody of a monoclonal antibody preparation is directed against a single determinant on an antigen. Thus, the modifier "monoclonal" indicates the character of the antibody as being obtained from a population of substantially homogeneous antibodies and is not to be construed as requiring production of the antibody by any particular method. For example, monoclonal antibodies used in accordance with the present invention may be produced by a variety of techniques, including, but not limited to, hybridoma methods, recombinant DNA methods, phage display methods, and methods utilizing transgenic animals containing all or part of the human immunoglobulin loci, or a combination thereof.

[0031] "Conserved portion" is intended to mean any portion of the wild-type counterpart of an oncogenic fusion protein that is conserved in the oncogenic fusion protein.

[0032] Specific binding: As used herein, the phrases "specific binding," "specifically binds to," or "specific for" refer to a measurable and reproducible interaction between a target and a specific detection reagent that determines the presence of the target in the presence of a heterogeneous population of molecules, including biological molecules. For example, an antibody that specifically binds to a target is one that binds to this target with higher affinity, avidity, more readily, and / or with a longer duration than it binds to other targets. In one embodiment, the extent to which a specific detection reagent binds to an unrelated target is less than about 10% of the binding of an antibody to the target, as measured, for example, by radioimmunoassay (RIA). In certain embodiments, a biomarker-specific reagent that specifically binds to a target has a dissociation constant (Kd) of 1 μM or less, 100 nM or less, 10 nM or less, 1 nM or less, or 0.1 nM or less. In another embodiment, specific binding can include, but does not require, exclusive binding.

[0033] Specific detection reagent: Any composition of matter capable of specifically binding to a target chemical structure in the context of a cell sample.

[0034] Stain: When used as a noun, the term "stain" shall refer to any substance that can be used to visualize specific molecules or structures in a cell sample for microscopic analysis, including bright field microscopy, fluorescence microscopy, electron microscopy, etc. When used as a verb, the term "stain" shall refer to any process that results in the deposition of a colorant on a cell sample.

[0035] Subject: As used herein, the term "subject" or "individual" refers to a mammal. Mammals include, but are not limited to, domesticated animals (e.g., cows, sheep, cats, dogs, horses, etc.), primates (e.g., humans, non-human primates such as monkeys), rabbits, rodents (e.g., mice, rats, etc.), and the like. In certain embodiments, the individual or subject is a human.

[0036] Test sample: A tumor sample obtained from a subject whose outcome is unknown at the time the sample is obtained.

[0037] Tissue sample: As used herein, the term "tissue sample" is intended to refer to a cell sample that preserves the cross-sectional spatial relationships between cells that were present within the subject from which the sample was obtained.

[0038] Tumor sample: A tissue sample obtained from a tumor.

[0039] II. Staining method The present disclosure is based on affinity histochemically or cytochemically stained samples of non-neuroendocrine NTRK fusion proteins using a first biomarker-specific reagent targeting one or more retained portions of TrkA, TrkB, and TrkC. The biomarker-specific reagent is selected by identifying the breakpoint of the wild-type protein that results in the fusion protein and targeting the portion of the wild-type protein that flanks the breakpoint that is retained in the fusion protein. Many resources are available for identifying fusion protein breakpoints, including the COSMIC database, which includes annotations of breakpoints by genomic location and the first exon expressed in the resulting fusion protein. Exemplary wild-type protein sequences are shown in Table 1. [Table 1]

[0040] Exemplary breakpoints and consensus retention portions for fusion proteins retaining the C-terminus of TrkA, TrkB, or TrkC are shown in Table 2. [Table 2]

[0041] In one embodiment, the biomarker-specific reagent specifically binds to one or more retention portions of TrkA, TrkB, and TrkC. In one embodiment, the biomarker-specific reagent specifically binds to each retention portion of TrkA, TrkB, and TrkC. An alignment between exemplary retention portions of TrkA, TrkB, and TrkC is shown in FIG. 1. In another specific embodiment, the biomarker-specific reagent specifically binds to one or more of the following: (a) an amino acid sequence comprising, consisting essentially of, or consisting of residues 363-760 of SEQ ID NO:1; (b) an amino acid sequence comprising, consisting essentially of, or consisting of residues 646-838 of SEQ ID NO:2; or (c) an amino acid sequence comprising, consisting essentially of, or consisting of residues 718-839 of SEQ ID NO:3. In another specific embodiment, the biomarker-specific reagent specifically binds to: (a) an amino acid sequence comprising, consisting essentially of, or consisting of residues 363-760 of SEQ ID NO:1; (b) an amino acid sequence comprising, consisting essentially of, or consisting of residues 646-838 of SEQ ID NO:2; and (c) an amino acid sequence comprising, consisting essentially of, or consisting of residues 718-839 of SEQ ID NO:3.

[0042] A biomarker-specific reagent can be any type of entity useful for the in situ detection (such as by histological or cytological staining) of a protein expressed by a cell sample. Exemplary biomarker-specific reagents include antibodies and antigen-binding fragments thereof, as well as ADNECTIN (a scaffold based on the 10th FN3 fibronectin; Bristol-Myers-Squibb Co.), AFFIBODY (a scaffold based on the Z domain of protein A from S. aureus; Affibody AB, Solna, Sweden), AVIMER (a scaffold based on domain A / LDL receptor; Amgen, Thousand Oaks, CA), dAb (a scaffold based on VH or VL antibody domains; GlaxoSmithKline PLC, Cambridge, UK), DARPin (a scaffold based on ankyrin repeat proteins; Molecular Partners AG, Zurich, Switzerland), ANTICALIN (a scaffold based on lipocalin; Pieris AG, Philly, Germany), NANOBODY (a scaffold based on VHH (camelid Ig); Ablynx), and other biomarker-specific reagents. Examples of engineered specific binding compositions include tetranectin (C-type lectin domain (CTLD)-based scaffolds), such as tetranectin (Borean Pharma A / S, Aarhus, Denmark), SMIP (Emergent Biosolutions, Inc., Rockville, Maryland), and tetranectin (C-type lectin domain (CTLD)-based scaffolds), such as tetranectin (Borean Pharma A / S, Aarhus, Denmark). A description of such engineered specific binding structures is outlined in Wurch et al., "Development of Novel Protein Scaffolds as Alternatives to Whole Antibodies for Imaging and Therapy: Status on Discovery Research and Clinical Validation," Current Pharmaceutical Biotechnology, Vol. 9, pp. 502-509 (2008), the contents of which are incorporated by reference.

[0043] In certain embodiments, the biomarker-specific reagent is an antibody. In another specific embodiment, the antibody is a monoclonal antibody (such as a mouse monoclonal antibody or a rabbit monoclonal antibody). In another specific embodiment, the antibody specifically binds to one or more conserved portions of TrkA, TrkB, or TrkC. In another specific embodiment, the antibody specifically binds to an epitope contained in one or more of the following: (a) an amino acid sequence comprising, consisting essentially of, or consisting of residues 363-760 of SEQ ID NO:1; (b) an amino acid sequence comprising, consisting essentially of, or consisting of residues 646-838 of SEQ ID NO:2; or (c) an amino acid sequence comprising, consisting essentially of, or consisting of residues 718-839 of SEQ ID NO:3. In another specific embodiment, the antibody specifically binds to: (a) an amino acid sequence comprising, consisting essentially of, or consisting of residues 363-760 of SEQ ID NO: 1; (b) an amino acid sequence comprising, consisting essentially of, or consisting of residues 646-838 of SEQ ID NO: 2; and (c) an amino acid sequence comprising, consisting essentially of, or consisting of residues 718-839 of SEQ ID NO: 3. In one embodiment, the antibody is a commercially available antibody according to Table 3. [Table 3]

[0044] In a specific embodiment, the antibody is EPR17341.

[0045] Biomarker-specific reagents are used to histochemically or cytochemically affinity stain samples suspected of containing NTRK fusion proteins. Affinity histochemical and cytochemical staining techniques typically involve contacting a sample deposited on a slide or other solid support with a biomarker-specific reagent under conditions sufficient to allow specific binding between the biomarker-specific reagent and the biomarker of interest. Binding of the biomarker-specific reagent to the biomarker facilitates deposition of a detectable moiety on the sample near the location containing the biomarker. The detectable moiety can be used to identify and / or quantify the biomarker to which the biomarker-specific reagent is directed. The presence and / or relative amount of the target in the sample can then be detected by detecting the signal generated by the detectable moiety.

[0046] The staining process may be manual, automated, or a combination of manual and automated steps. In one embodiment, the staining process may be performed on an automated, advanced staining platform. An automated, advanced staining platform typically includes at least the following: reservoirs for the various reagents used in the staining protocol, a reagent dispensing unit in fluid communication with the reservoirs for dispensing the reagents onto the slides, a waste removal system for removing used reagents and other waste from the slides, and a control system for coordinating the operation of the reagent dispensing unit and the waste removal system. In addition to performing the staining process, many automated slide stainers can also perform (or are compatible with other systems that perform) steps incidental to staining, including slide baking (to adhere the sample to the slide), dewaxing (also called deparaffinization), epitope inactivation, counterstaining, dehydration and clearing, and mounting. Prichard describes several specific examples and various features of automated IHC / ISH slide stainers, including the intelliPATH (Biocare Medical), WAVE (Celerus Diagnostics), DAKO OMNIS and DAKO AUTOSTAINER LINK 48 (Agilent Technologies), BENCHMARK (Ventana Medical Systems, Inc.), Leica BOND, and Lab Vision Autostainer (Thermo Scientific) automated slide stainers. Additionally, Ventana Medical Systems, Inc. is the assignee of several United States patents that disclose systems and methods for performing automated analyses, including U.S. Patent Nos. 5,650,327, 5,654,200, 6,296,809, 6,352,861, 6,827,901, and 6,943,029, and U.S. Published Patent Application Nos. 20030211630 and 20040052685, each of which is incorporated herein by reference in its entirety.Commercially available staining units typically operate on one of the following principles: (1) open individual slide staining, in which the slide is positioned horizontally and reagents are dispensed as a puddle onto the surface of the slide containing the tissue sample (as implemented, for example, in the DAKO AUTOSTAINER Link 48 (Agilent Technologies) and intelliPATH (Biocare Medical) stainers); (2) liquid overlay technique, in which reagents are either covered by or dispensed through an inert fluid layer deposited on the sample (as implemented, for example, in the VENTANA BenchMark and DISCOVERY stainers); or (3) capillary gap staining, in which the slide surface is placed near another surface (such as another slide or a cover plate) to create a narrow gap through which capillary forces draw the liquid reagents and keep them in contact with the sample (as in the staining principle used in the DAKO TECHMATE, Leica BOND, and DAKO OMNIS stainers). During several repetitions of capillary gap staining, the liquid in the gap does not mix (as in the DAKO TECHMATE and Leica BOND). A variation of capillary gap staining, called dynamic gap staining, uses capillary forces to apply the sample to the slide and then translates parallel surfaces into each other to agitate and mix the reagents during incubation (such as the staining principle implemented in the DAKO OMNIS slide stainer (Agilent)). In translation gap staining, a translatable head is placed on the slide. The underside of the head is separated from the slide by a first gap small enough to allow a meniscus of liquid to form from the liquid on the slide during slide translation. A mixing extension, having a lateral dimension smaller than the width of the slide, extends from the underside of the translatable head to define a second gap between the mixing extension and the slide that is smaller than the first gap.During translation of the head, the lateral dimension of the mixing extension is sufficient to generate a lateral movement in the liquid on the slide, generally in a direction extending from the second gap to the first gap. See WO 2011 / 139978 A1. The use of inkjet technology to deposit reagents on slides has recently been proposed. See WO 2016-170008 A1. This list of staining techniques is not intended to be comprehensive, and fully or semi-automated systems for performing biomarker staining can be used.

[0047] The staining method is performed on a cell sample of the suspected tissue, including a tissue sample and a cytological sample. In some embodiments, the cell sample is obtained from a subject having or suspected of having a tumor. In some embodiments, the sample includes cells obtained directly from the tumor. In some embodiments, the tumor is a solid tumor, such as a carcinoma, lymphoma, or sarcoma. In one embodiment, the tumor is a non-neuroendocrine tumor. In one embodiment, the non-neuroendocrine tumor is a solid tumor of the salivary gland, thyroid, skin, breast, head and / or neck, lung, upper gastrointestinal tract (including esophagus and stomach), female reproductive system (including tumors of the uterus, fallopian tubes, and ovaries), lower gastrointestinal tract (including tumors of the colon, rectum, and anus), genitourinary, exocrine, endocrine, renal, or lymphoid origin. In one embodiment, the subject has melanoma, salivary gland cancer, thyroid cancer, breast cancer, ovarian cancer, pancreatic cancer, head and neck cancer, lung cancer, esophageal cancer, gastric cancer (excluding gastrointestinal stromal tumors (GISTs)), colorectal cancer (including cancer of the colon, rectum, and anus), prostate cancer, urothelial cancer, or lymphoma.

[0048] When a tissue sample is used, the tissue sample is processed in a manner compatible with histochemical staining, including, for example, fixation, embedding in a wax matrix (such as paraffin), and sectioning (such as by a microtome). No specific processing steps are required by the present disclosure, as long as the obtained sample is compatible with histochemical staining of the sample with a set of biomarker-specific reagents. In certain embodiments, microtome sections of formalin-fixed, paraffin-embedded (FFPE) samples are used in the staining process. When a cytological sample is used, the sample is fixed with formalin.

[0049] Depending on the biomarker-specific reagent and sample being used, the sample may be subjected to an epitope retrieval process (also called antigen retrieval) before application of the biomarker-specific reagent. Exemplary epitope retrieval processes include heat-induced epitope retrieval (HIER), which involves heating the sample in various buffers at different pH levels; protease-based epitope retrieval (PBER), in which the sample is digested with a proteolytic enzyme before staining; and a combination of HIER and PBER. Various specific epitope retrieval processes have been reviewed by Shi et al., D'Amico et al., Yamashita et al., Vinod et al., and Warford et al., but these are not exhaustive. Whether epitope retrieval is performed and the specific form of epitope retrieval used will depend on the particular biomarker-specific reagent chosen and may need to be empirically determined for each biomarker-specific reagent used.

[0050] Depending on the reagents and sample used, it may be desirable to block endogenous protein activity before adding biomarker-specific and / or detection reagents. For example, if the detection reagent relies on biotin and a biotin-binding protein, it may be necessary to block endogenous biotin using, for example, free, unlabeled biotin-binding protein. Similarly, many detection schemes rely on the activity of enzymes such as phosphatases and peroxidases, requiring neutralization of endogenous enzymes with similar activity. Commercially available kits are available for such blocking processes, such as Endogenous Biotin Blocking Kit (Cat. No. E21390, ThermoFisher Scientific), Endogenous Avidin / Biotin Blocking Kit (Cat. No. ab64212, Abcam, plc.), Endogenous Biotin Blocking Kit Cat. No. 760-050, Ventana Medical Systems, Inc.), Hydrogen Peroxide Blocking Reagent (Cat. No. ab64218, Abcam plc.), Peroxidase and Alkaline Phosphatase Blocking Reagent (Code S2003, Agilent Technologies), among others.

[0051] Before applying a biomarker-specific reagent to the sample, it may also be useful to block sites on the sample to which the biomarker-specific reagent may nonspecifically bind. Common blocking agents include eBioscience™ IHC / ICC Blocking Buffer - High Protein (Cat. No. 00-4952-54, ThermoFisher Scientific), eBioscience™ IHC / ICC Blocking Buffer - Low Protein (Cat. No. 00-4953-54, ThermoFisher Scientific), DISCOVERY Antibody Block (Cat. No. 760-4204, Ventana Medical Systems, Inc.), as well as normal serum buffer, nonfat dry milk, BSA (bovine serum albumin), and gelatin, among others.

[0052] Washing steps can be performed after each of these pretreatment steps by applying one or more passes of a wash buffer. The wash buffer is typically a neutral buffered saline solution, which may contain a small amount of detergent. Exemplary wash buffers include, for example, phosphate-buffered saline (PBS), PBS-Tween 20, Tris-buffered saline (TBS), TBS-Tween 20 (polysorbate 20), Tris-HCl, Tris-HC-Tween 20, phosphate buffer (PB), AP buffer, etc.

[0053] Once the sample is prepared for staining, a biomarker-specific reagent is applied to the sample and incubated for a time and under conditions sufficient to promote specific binding between the biomarker and the biomarker-specific reagent. A wash step may be performed after incubating the sample with the biomarker-specific reagent by applying one or more passes of a wash buffer. This removes unbound or nonspecifically bound biomarker-specific reagent from the sample, reducing off-target and / or background staining.

[0054] Detection of biomarkers in a sample is achieved by depositing a detectable moiety in close proximity to a biomarker-specific reagent bound to the sample. In some cases, the detectable moiety is directly attached to the biomarker-specific reagent, so that it is deposited on the sample when the biomarker-specific reagent binds to its target (commonly referred to as direct labeling). In other embodiments, deposition of the detectable moiety is achieved by applying a set of detection reagents to the sample after application of the biomarker-specific reagent, where the detection reagents bind to or otherwise react with the biomarker-specific reagent in a manner that results in deposition of the detectable moiety (commonly referred to as indirect labeling).

[0055] In some embodiments where an indirect method is used, the detectable moiety is deposited via an enzymatic reaction localized on the biomarker-specific reagent. Enzymes suitable for such reactions are well known and include, but are not limited to, oxidoreductases, hydrolases, and peroxidases. Specific enzymes explicitly mentioned are horseradish peroxidase (HRP), alkaline phosphatase (AP), acid phosphatase, glucose oxidase, β-galactosidase, β-glucuronidase, and β-lactamase. The enzyme may be directly bound to the biomarker-specific reagent or may be indirectly associated with the biomarker-specific reagent via a labeled conjugate. As used herein, "labeled conjugate" includes: (a) a specific detection reagent; and (b) An enzyme linked to a specific detection reagent, which reacts with a chromogenic substrate, a signaling conjugate and / or an enzyme-reactive dye under appropriate reaction conditions to produce a dye in situ and / or deposit the dye on a tissue sample.

[0056] In non-limiting examples, the specific detection reagent of the label conjugate can be a secondary detection reagent (such as a species-specific secondary antibody bound to a primary antibody, an anti-hapten antibody bound to a hapten-conjugated primary antibody, or a biotin-binding protein bound to a biotinylated primary antibody), a tertiary detection reagent (such as a species-specific tertiary antibody bound to a secondary antibody, an anti-hapten antibody bound to a hapten-conjugated secondary antibody, or a binding protein bound to a biotinylated secondary antibody), or other such arrangements. Enzymes localized to biomarker-specific reagents bound in this manner to the sample can be used in a number of schemes to deposit detectable moieties.

[0057] In some cases, the enzyme reacts with a chromogenic compound / chromogenic substrate. Specific, non-limiting examples of chromogenic compounds / chromogenic substrates include 4-nitrophenyl phosphate (pNPP), Fast Red, bromochloroindolyl phosphate (BCIP), nitroblue tetrazolium (NBT), BCIP / NBT, Fast Red, AP Orange, AP Blue, tetramethylbenzidine (TMB), 2,2'-azino-di-[3-ethylbenzothiazoline sulfonate] (ABTS), o-dianisidine, 4-chloronaphthol (4-CN), nitrophenyl-β-D-galactopyranoside (ONPG), Examples of suitable antibacterial agents include o-phenylenediamine (OPD), 5-bromo-4-chloro-3-indolyl-β-galactopyranoside (X-Gal), methylumbelliferyl-β-D-galactopyranoside (MU-Gal), p-nitrophenyl-α-D-galactopyranoside (PNP), 5-bromo-4-chloro-3-indolyl-β-D-glucuronide (X-Gluc), 3-amino-9-ethylcarbazole (AEC), fuchsin, iodonitrotetrazolium (INT), tetrazolium blue, and tetrazolium violet.

[0058] In some embodiments, enzymes can be used in metallographic detection schemes. Metallographic detection methods involve the use of an enzyme, such as alkaline phosphatase, in combination with a water-soluble metal ion and a redox-inactive substrate for the enzyme. In some embodiments, the substrate is converted by the enzyme into a redox-active agent, which reduces the metal ion, causing it to form a detectable precipitate. (See, e.g., U.S. Patent Application No. 11 / 015,646, filed December 20, 2004; PCT Publication No. 2005 / 003777; and U.S. Patent Application Publication No. 2004 / 0265922; each of which is incorporated herein by reference in its entirety.) Metallographic detection methods involve the use of an oxidoreductase (such as horseradish peroxidase) in combination with a water-soluble metal ion, an oxidizing agent, and a reducing agent to form a detectable precipitate. (See, e.g., U.S. Patent No. 6,670,113, incorporated herein by reference in its entirety.)

[0059] In some embodiments, the enzymatic action occurs between the enzyme and the dye itself, and the reaction converts the dye from an unbound species to a species that is deposited on the sample. For example, the reaction of DAB with a peroxidase (such as horseradish peroxidase) oxidizes and precipitates the DAB.

[0060] In yet other embodiments, the detectable moiety is deposited via a signaling conjugate that includes a latent reactive moiety configured to react with an enzyme to form a reactive species that can bind to the sample or other detection components. These reactive species can react with the sample proximal to their generation, i.e., near the enzyme, but rapidly convert to a non-reactive species, so that the signaling conjugate is not deposited at a site distal to the site where the enzyme is deposited. Examples of latent reactive moieties include quinone methide (QM) analogs, such as those described in WO2015124703A1, and tyramide conjugates, such as those described in WO2012003476A2, each of which is incorporated herein by reference in its entirety. In some examples, the latent reactive moiety is directly conjugated to a dye, such as N,N'-biscarboxypentyl-5,5'-disulfonato-indo-dicarbocyanine (Cy5), 4-(dimethylamino)azobenzene-4'-sulfonamide (DABSYL), tetramethylrhodamine (DISCO Purple), and rhodamine 110 (rhodamine). In other examples, the latent reactive moiety is conjugated to one member of a specific binding pair and the dye is conjugated to the other member of the specific binding pair. In other examples, the latent reactive moiety is linked to one member of a specific binding pair and an enzyme is linked to the other member of the specific binding pair, where the enzyme (a) reacts with a chromogenic substrate to result in the production of a dye or (b) is reactive with a dye to result in the deposition of the dye (such as DAB). Examples of specific binding pairs include:

[0061] (1) biotin or a biotin derivative (such as desthiobiotin) linked to a potentially reactive moiety, and a biotin-binding entity (such as avidin, streptavidin, deglycosylated avidin (such as NEUTRAVIDIN), or a biotin-binding protein (such as CAPTAVIDIN) with a nitrated tyrosine at its biotin-binding site linked to a dye or enzyme reactive with a chromogenic substrate or dye (e.g., peroxidase linked to a biotin-binding protein when the dye is DAB); and (2) A hapten linked to a potentially reactive moiety and an anti-hapten antibody linked to a dye or to an enzyme reactive with a chromogenic substrate or reactive with a dye (e.g., peroxidase linked to a biotin-binding protein when the dye is DAB).

[0062] Specifically included are non-limiting examples of biomarker-specific reagent and detection reagent combinations set forth in Table 4. [Table 4] TIFF0007757382000005.tif254170TIFF0007757382000006.tif252170TIFF0007757382000007.tif253170TIFF0007757382000008.tif253170 TIFF0007757382000009.tif254170TIFF0007757382000010.tif255170TIFF0007757382000011.tif253170TIFF0007757382000012.tif104170

[0063] In certain embodiments, the biomarker-specific reagents and specific detection reagents shown in Table 4 are antibodies. As will be appreciated by one of skill in the art, the detection schemes for each of the biomarker-specific reagents may be the same or different.

[0064] Non-limiting examples of commercially available detection reagents or kits containing detection reagents suitable for use in the methods of the invention include the VENTANA ultraView detection system (secondary antibodies conjugated to enzymes, including HRP and AP), the VENTANA iVIEW detection system (biotinylated anti-species secondary antibodies and streptavidin-conjugated enzymes), the VENTANA OptiView detection system (OptiView) (anti-species secondary antibodies conjugated to haptens and anti-hapten tertiary antibodies conjugated to enzyme multimers), the VENTANA Amplification kit (unconjugated secondary antibodies that can be used with any of the previous VENTANA detection systems to amplify the number of enzymes at the site of primary antibody binding), the VENTANA OptiView Amplification systems (which include an anti-species secondary antibody conjugated to a hapten, an anti-hapten tertiary antibody conjugated to an enzyme multimer, and a tyramide conjugated to the same hapten. In use, the secondary antibody is contacted with the sample, resulting in binding to the primary antibody. The sample is then incubated with the anti-hapten antibody to associate the enzyme with the secondary antibody. The sample is then incubated with tyramide, resulting in deposition of additional hapten molecules. The sample is then incubated again with the anti-hapten antibody, resulting in deposition of additional enzyme molecules. The sample is then incubated with a detectable moiety, resulting in pigmentation), VENTANA DISCOVERY, DISCOVERY OmniMap, DISCOVERY UltraMap anti-hapten antibody, secondary antibody, chromogen, fluorophore, and dye kits, each of which is available from Ventana Medical Systems, Inc. (Tucson, Arizona), PowerVision and PowerVision+ IHC Detection Systems (secondary antibodies that polymerize directly with HRP or AP into compact polymers with high enzyme-to-antibody ratios), and DAKO Available from the EnVision™+ System (an enzyme-labeled polymer that binds to a secondary antibody).

[0065] If necessary, biomarker-stained slides can be counterstained to help identify morphologically relevant regions. Examples of counterstains include chromogenic nuclear counterstains such as hematoxylin (stains blue to purple), methylene blue (stains blue), toluidine blue (stains nuclei dark blue and polysaccharides pink to red), nuclear fast red (also known as Kernectrodt stain, stains red), and methyl green (stains green); non-nucleogenic stains such as eosin (stains pink); 4',6-diamino-2-phenylindole (DAPI, stains blue), propidium iodide (stains red), Hoechst stain (stains blue), nuclear green DCS1 (stains green), and nuclear Fluorescent non-nuclear stains such as Fluorophore-labeled phalloidin (stains filamentous actin, color depends on the conjugated fluorophore);

[0066] III. Staining evaluation In one embodiment, a set of stained samples generated by the presently disclosed methods is used to determine the presence or absence of a fusion protein in a patient sample. Typically, a sample is obtained from a patient and prepared for analysis as described above. A portion of the sample (e.g., an initial tissue section from a biopsy of a tumor resection sample, or an initial slide prepared from a cytological sample of tumor cells (e.g., a cytological smear (e.g., an endocervical smear), a fine needle aspirate, isolated circulating tumor cells, etc.) is prepared and stained with a biomarker-specific reagent. The stained sample is then scored for the percentage of cellular staining and / or the percentage of cells stained at or above a predetermined threshold level. Preferably, the sample is fixed with formalin solution. In one embodiment, the threshold staining intensity is at least 1.5+, and the threshold level of tumor cells having the threshold staining intensity is in the range of 25%-75%. In one embodiment, the threshold staining intensity is at least 1.5+, and the threshold level of tumor cells having the threshold staining intensity is in the range of 50%-75%. In one embodiment, the threshold staining intensity is at least 1.5+ and the threshold level of tumor cells having the threshold staining intensity is 60%. In one embodiment, the threshold staining intensity is at least 1.5+ and the threshold level of tumor cells having the threshold staining intensity is 75%. In one embodiment, the threshold staining intensity is at least 2+ and the threshold level of tumor cells having the threshold staining intensity is in the range of 25%-75%. In one embodiment, the threshold staining intensity is at least 2+ and the threshold level of tumor cells having the threshold staining intensity is 50%. In one embodiment, the threshold staining intensity is at least 2+ and the threshold level of tumor cells having the threshold staining intensity is 60%. In one embodiment, the threshold staining intensity is at least 2+ and the threshold level of tumor cells having the threshold staining intensity is 75%.

[0067] In some cases, stained samples are stratified based on expression patterns and scored using a scoring method specific to the staining pattern. For example, if a fixed gradient is observed, a first scoring methodology is applied to samples with a cytoplasmic and / or membrane expression pattern, and a second scoring methodology is applied to samples with nuclear localization. For example, samples with a cytoplasmic and / or membrane staining pattern can be scored by determining whether the sample meets or exceeds a threshold level of tumor cells at or above a threshold staining intensity considered positive for the TRK fusion protein. In one embodiment, the threshold staining intensity is at least 1.5+, and the threshold level of tumor cells with the threshold staining intensity is in the range of 25% to 75%. In one embodiment, the threshold staining intensity is at least 1.5+, and the threshold level of tumor cells with the threshold staining intensity is 50%. In one embodiment, the threshold staining intensity is at least 1.5+, and the threshold level of tumor cells with the threshold staining intensity is 60%. In one embodiment, the threshold staining intensity is at least 1.5+, and the threshold level of tumor cells with the threshold staining intensity is 75%. In one embodiment, the threshold staining intensity is at least 2+, and the threshold level of tumor cells having the threshold staining intensity is in the range of 25% to 75%. In one embodiment, the threshold staining intensity is at least 2+, and the threshold level of tumor cells having the threshold staining intensity is 50%. In one embodiment, the threshold staining intensity is at least 2+, and the threshold level of tumor cells having the threshold staining intensity is 60%. In one embodiment, the threshold staining intensity is at least 2+, and the threshold level of tumor cells having the threshold staining intensity is 75%.

[0068] As another example, a sample with a nuclear staining pattern can be scored by determining whether the minimum contiguous tumor cell area of ​​the sample has a concentration of tumor cells that stain at or above a threshold expression level. In one embodiment, the threshold contiguous tumor cell area is at least 20 cells, the threshold staining intensity is any specific staining relative to background, and the threshold percentage of cells is in the range of 25%-75% or 25%-80%. In another embodiment, the threshold contiguous tumor cell area is at least 20 cells, the threshold staining intensity is any specific staining relative to background, and the threshold percentage of cells is at least 75%. In another embodiment, the threshold contiguous tumor cell area is at least 20 cells, the threshold staining intensity is any specific staining relative to background, and the threshold percentage of cells is at least 80%. In one embodiment, the threshold contiguous tumor cell area is at least 20 cells, the threshold staining intensity is 0.5 or greater, and the threshold percentage of cells is in the range of 25%-75% or 25%-80%. In another embodiment, the threshold adjacent tumor cell area is at least 20 cells, the threshold staining intensity is 0.5+ or greater, and the threshold percentage of cells is at least 75%. In another embodiment, the threshold adjacent tumor cell area is at least 20 cells, the threshold staining intensity is 0.5+ or greater, and the threshold percentage of cells is at least 80%. In one embodiment, the threshold adjacent tumor cell area is at least 50 cells, the threshold staining intensity is any specific staining relative to background, and the threshold percentage of cells is in the range of 25%-75% or 25%-80%. In another embodiment, the threshold adjacent tumor cell area is at least 50 cells, the threshold staining intensity is any specific staining relative to background, and the threshold percentage of cells is at least 75%. In another embodiment, the threshold adjacent tumor cell area is at least 50 cells, the threshold staining intensity is any specific staining relative to background, and the threshold percentage of cells is at least 80%. In one embodiment, the threshold contiguous tumor cell area is at least 50 cells, the threshold staining intensity is 0.5+ or greater, and the threshold percentage of cells is in the range of 25%-75% or 25%-80%.In another embodiment, the threshold contiguous tumor cell area is at least 50 cells, the threshold staining intensity is 0.5+ or greater, and the threshold percentage of cells is at least 75%. In another embodiment, the threshold contiguous tumor cell area is at least 50 cells, the threshold staining intensity is 0.5+ or greater, and the threshold percentage of cells is at least 80%.

[0069] VI. Clinical Applications In one embodiment, the assays described herein are used to characterize tumor samples from patients. For example, biopsy or resection samples are obtained, fixed, embedded in paraffin, sectioned, and stained. The stained sections are scored as described above. In some embodiments, tumors with scores indicating the presence of fusion protein are characterized as "fusion positive," while tumors with scores not indicating the presence of fusion protein are characterized as "fusion negative." In other embodiments, cells in the intermediate category between "fusion positive" and "fusion negative" are characterized as "borderline." For example, if the scoring method is based on a threshold percentage of cells staining at or above a threshold level, the range of percentages below the threshold percentage is defined as "borderline," and all other samples with a percentage of cells falling below the borderline range are considered "fusion negative." As another example, if the scoring method is based on a threshold percentage of cells staining at or above a threshold level within a threshold tumor cell area, the percentage range below the threshold tumor cell area is defined as "borderline," and all other samples with a percentage of cells that falls below the borderline range are considered "fusion negative."

[0070] In some embodiments, the assay is used as a screening test to identify patients eligible for a nucleic acid-based assay to confirm the presence of a fusion protein. For example, samples can be screened for the presence or absence of a fusion protein using an assay, and only samples characterized as fusion-positive are subjected to a sequencing- or PCR-based assay to confirm the presence and / or identity of the fusion detected in the assay. In other embodiments, the assay is a reflex test to confirm the presence and expression of a fusion protein identified by a nucleic acid-based assay. For example, samples can be screened for the presence or absence of an NTRK gene rearrangement using a sequencing- or PCR-based assay, and only samples characterized as rearrangement-positive by a sequencing- or PCR-based assay are screened by the assay described herein to confirm the presence and / or expression of the fusion detected by the nucleic acid assay. In other embodiments, the characterization of the presence or absence of a fusion protein is based solely on the assay. In still other embodiments, samples characterized as "fusion-negative" or "borderline" can be screened for the presence of an NTRK gene rearrangement by a sequencing- or PCR-based assay, and cells characterized as "fusion-positive" are not screened.

[0071] In some embodiments, assays are used to select treatments for patients. For example, patients with tumors or samples characterized as "fusion positive" are given targeted therapy directed against wild-type counterparts, optionally in combination with standard treatment courses for tumors. Exemplary targeted therapy includes those listed in Table 5. [Table 5]

[0072] Patients with tumors or samples characterized as fusion-negative receive standard treatment, which does not include targeted therapy against the wild-type counterpart.

[0073] VIII. Working Examples To assess whether a scoring algorithm could be developed that could predict the presence of Trk fusions across tumor types, IHC staining and analysis of over 3000 tissues across multiple indications was performed.

[0074] Formalin-fixed, paraffin-embedded (FFPE) normal and neoplastic tissues were commercially obtained and screened with a prototype IHC assay using the pan-TRK antibody clone EPR17341, which involved heat-induced epitope retrieval followed by antibody incubation and colorimetric development using OptiView DAB Detection (RTD, Tucson, AZ) on a BenchMark ULTRA automated slide stainer (RTD, Tucson, AZ).

[0075] A subset of cases, mostly with specific staining by the pan-TRK (EPR17341) assay, were further evaluated by in situ hybridization (ISH) using NTRK1, 2, and 3 break-apart probes. The NTRK1, 2, and 3 break-apart oligo probes consisted of two pools of oligonucleotides (oligos) targeting genomic regions spanning the 5' and 3' ends of the NTRK1, 2, and 3 genes, respectively. DNP and fluorescein haptens were attached to the oligos in a basic intercalation configuration during synthesis using DNP-TEG phosphoramidite (Link Technologies Ltd, Bellshill, Lanarkshire) and 6-fluorescein phosphoramidite (Link Technologies Ltd, Bellshill, Lanarkshire). The synthesized oligos were purified using reverse-phase cartridges, and mass spectrometry analysis was performed to confirm removal of truncated oligos.

[0076] The criteria used to define the break-apart status of the ISH assay were determined based on evaluation of the mean break-apart rate in normal tissues and tumors lacking pan-TRK IHC expression. Tumors with a break-apart rate greater than 5 standard deviations above the mean were considered to represent true NTRK gene fusions.

[0077] Representative images of pan-TRK staining across various tumor types with various genotypes are shown in Figures 2A-2B. Nine percent of tumors (n = 324) showed specific pan-TRK IHC staining, defined as >0% of tumor cells staining (range: 0%-54% for gastric and salivary gland cancers, respectively). When only specimens with IHC specific staining in >10% and >25% of tumor cells were considered, the overall percentage of cases with specific staining decreased to 5% (n = 191) and 4% (n = 133), respectively.

[0078] One hundred sixty-four cases showing IHC staining were available for ISH testing. Of these, 12 were found to harbor NTRK fusions (five CRCs, two melanomas, two papillary thyroid carcinomas, two salivary gland carcinomas, and one pancreatic carcinoma). The proportion of pan-TRK-positive cases at various tumor cell staining percentages by tumor type, including the results of confirmatory ISH testing, is shown in Table 6. [Table 6]

[0079] Although staining intensity and tumor cell staining rate varied by tissue type, cases with fusions tended to have higher staining intensity and a higher percentage of tumor cells (see Figures 3A and 3B). Figures 3A and 3B show the distribution of ISH-confirmed samples by tumor cell staining percentage (0-100%) and staining intensity (0-3+). Circles represent fusion-negative cases, and triangles represent fusion-positive cases. Colors represent various tumor histologies. Figure 3A shows the staining distribution of tumor types, including ISH-confirmed fusion-positive cases, within our dataset, while Figure 3B shows the staining distribution of neuroendocrine tumors, in which no fusion-positive cases were detected.

[0080] The results in terms of percent tumor cell staining by IHC for all tumors in the dataset are shown in Table 7. [Table 7]

[0081] Of the cases in which IHC specific staining was greater than 0% of tumor cells, 12 / 164 (7%) demonstrated the presence of NTRK fusions by ISH. Of the cases in which IHC specific staining was greater than 25% of tumor cells, 10 / 88 (11%) demonstrated the presence of fusions by ISH (Table 6). Tumors demonstrating fusions by ISH tended to stain with higher intensity and in a higher percentage of tumors by pan-TRK IHC (upper right quadrant; Figure 3A) than non-fusion tumors, with the exception of neuroendocrine tumors (Figure 3B). Using a higher criterion for IHC specific positive staining (>25%), two fusion-positive melanomas were excluded from ISH testing (Table 6). These two tissue samples stained poorly by IHC, showing evidence of a fixation gradient. Importantly, these tissues showed high-intensity nuclear staining in a high percentage (>90%) of adjacent cells in areas unaffected by fixation-related artifact.

[0082] Figure 4 shows the subcategorization of solid tumors based on IHC and ISH testing.

[0083] Examples of observed staining patterns are shown in Figures 5 and 6. As shown in Figure 5, the staining patterns sometimes included membrane staining (A), cytoplasmic staining (A-C), and nuclear staining (C). Figure 7 shows that a fixation gradient occurred in some samples, which may affect the staining level of some cells. It was noted that samples with nuclear localization were more sensitive to the fixation gradient than samples with cytoplasmic / membrane localization.

[0084] In summary, pan-TRK IHC staining varied in both staining intensity and tumor cell percentage depending on tumor type. Solid tumors with ISH-based fusions showed higher intensity and a higher percentage of tumor cells with IHC staining than tumors with wild-type TRK protein expression, except for neuroendocrine and spindle cell tumors. In tumor types with a low prevalence of wild-type TRK protein expression (e.g., CRC and papillary thyroid carcinoma), pan-TRK IHC staining may be useful for identifying tumors with fusions. In contrast, in tumors with a high prevalence of wild-type TRK protein expression (e.g., neuroendocrine tumors and GISTs), the distribution of IHC staining percentage and intensity did not support a clear distinction between wild-type expression and fusions. According to Table 6, as the percentage of tumor cells stained by pan-TRK IHC increased, the number of specimens subjected to ISH (out of a total of 164 cases) gradually decreased, but this decrease did not impair the identification of tumors with NTRK gene fusions by ISH in well-preserved tissue. This metric, combined with increased IHC staining intensity, appears to further highlight tumors with NTRK gene fusions by ISH testing.

[0085] Two melanomas and one pancreatic ductal adenocarcinoma did not conform to the above observations. The observed lower percentage of tumor cell staining was likely related to fixation artifact. Interestingly, however, small areas of adjacent viable tumor showed a high percentage of highly intense nuclear staining.

[0086] VI. References The following references are incorporated herein by reference in their entirety: Amatu et al., NTRK gene fusions as novel targets of cancer therapy across multiple tumor types,ESMO Open,Vol.1,Issue 2,e000023 doi:10.1136 / esmoopen-2015-000023(2016). Bailey et al., Tropomyosin receptor kinase inhibitors: an updated patent review for 2010-2016-Part II, Expert Opinion on Therapetuic Patents, Vol. 27, Issue 7, pp. 831-49 (Mar. 2017). D'Amico et al., State of the art in antigen retrieval for immunohistochemistry, J Immunol Methods.Vol.341(1-2),pp.1-18(Feb.28,2009). Hechtman et al.,Pan-Trk Immunohistochemistry Is an Efficient and Reliable Screen for the Detection of NTRK Fusions,Am.J.Surg.Path.,Vol.41,Issue 11,pp.1547-51(Nov.2017). Prichard, Overview of Automated Immunohistochemistry, Arch Pathol Lab Med., Vol. 138, pp. 1578-1582 (2014) Shi et al.,Antigen retrieval immunohistochemistry:review and future prospects in research and diagnosis over two decades,J Histochem Cytochem,Vol.59,Issue 1,pp.13-32(Jan.2011). Stransky et al.,The landscape of kinase fusions in cancer,Nature Communications,Vol.5,Article No.4846(2014)doi:10.1038 / ncomms5846. Vinod et al.,A simple and effective heat induced antigen retrieval method,MethodsX,Vol.3,pp.315-19(published online Apr.8,2016). Warford et al.,Antigen retrieval,blocking,detection and visualisation systems in immunohistochemistry:A review and practical evaluation of tyramide and rolling circle amplification systems,Methods,Vol.70,Issue 1,pp.28-33(Nov.2014). Wellcome Sanger Institute,COSMIC-the Catalogue of Somatic Mutations in Cancer(COSMIC database),available at http: / / cancer.sanger.ac.uk / cosmic / fusion(last accessed 13-SEP-2018). Yamashita et al.,Mechanisms of Heat-induced Antigen Retrieval:Analyses In Vitro Employing SDS-PAGE and Immunohistochemistry,J.Histochemistry and Cytochemistry,Vol.53,Issue 1,pp.13-21(2005). Barbacid M.et al.Biochim.Biophys.Acta Rev.Cancer 1991. Barbacid M.Annals New York Academy of Sciences.1995:442-458. Lemmon MA and Schlessinger J.Cell 2010;141:1117-1134. Klein R et al.Cell 1991;85:189-197. Eide F et al.J.Neurosci.1996;16(10):3123-3129. Luberg K et al.BMC Neurosci.2015:16:78 DOI 10.1186 / s12868-015-0215-x. Vaishnavi A,et al.Nature Medicine.2013;19(11):1469-1472. De Braud FG et al.2014 ASCO Annual Meeting;Abstract 2502. Argani PM,et al.Mod Pathol.2000;13(1):29-36. Bishop JA et al.Hum Pathol.2013;44(10):1982-1988. Bourgeois JM et al.Am J Surg Pathol.2000;24(7):937-946. Rubin BP et al Am J Pathol.1998;153(5):1451-1458. Tognon C et al.Cancer Cell.2002;2:367-376. Brzezianska E et al.Mutat Res.2006;599(1-2):26-35. Fernandez-Cuesta L et al.105th Annual Meeting of the American Association for Cancer Research,2014,San Diego,California,AACR. Leeman-Neill RJ et al.Cancer.2014;120(6):799-807. Ross J.S et al.Oncologist.2014;19(3):235-242. Farago et al.JCO Precision Oncology.Published online July 23,2018. Gatalica Z et al.Mod Pathol.Published online 23 August 2018.

Claims

1. 1. A method for detecting a TrkA, TrkB, or TrkC fusion protein in a non-neuroendocrine tumor sample, comprising: affinity histochemical staining of said non-neuroendocrine tumor sample with antibodies that specifically bind to the following: an amino acid sequence comprising residues 363-760 of SEQ ID NO:1, an amino acid sequence comprising residues 646-838 of SEQ ID NO:2, and an amino acid sequence comprising residues 718-839 of SEQ ID NO:3; - detecting a membranous and / or cytoplasmic staining pattern in said non-neuroendocrine tumor sample; - scoring the non-neuroendocrine tumor sample as positive for a fusion protein involving TrkA, TrkB, or TrkC when a threshold percentage or more of tumor cells stain above a threshold staining intensity in the detected membrane and / or cytoplasmic staining pattern, wherein the threshold percentage of tumor cells is in the range of 25% to 75% and the threshold staining intensity is at least 1.5; A method comprising:

2. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 50% and the threshold staining intensity is 1.

5.

3. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 60% and the threshold staining intensity is 1.

5.

4. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 75% and the threshold staining intensity is 1.

5.

5. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 50% and the threshold staining intensity is 1.

75.

6. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 60% and the threshold staining intensity is 1.

75.

7. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 75% and the threshold staining intensity is 1.

75.

8. 2. The method of claim 1, wherein the threshold percentage of tumor cells is in the range of 25% to 75% and the threshold staining intensity is at least 2.

9. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 50% and the threshold staining intensity is 2.

10. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 60% and the threshold staining intensity is 2.

11. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 75% and the threshold staining intensity is 2.

12. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 50% and the threshold staining intensity is 3.

13. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 60% and the threshold staining intensity is 3.

14. 2. The method of claim 1, wherein the threshold percentage of tumor cells is 75% and the threshold staining intensity is 3.

15. The affinity histochemical staining (a) subjecting the non-neuroendocrine tumor sample to a heat-induced epitope retrieval process; and (b) contacting the non-neuroendocrine tumor sample with a set of antibodies and detection reagents to deposit a brightfield dye near any antibodies bound to the non-neuroendocrine tumor sample; The method of claim 1 , comprising:

16. 16. The method of claim 15, wherein the set of detection reagents comprises a set of a secondary antibody immunoreactive with the antibody, a tertiary antibody conjugated to an enzyme and immunoreactive with the secondary antibody, and a reagent reactive with the enzyme that results in the deposition of a brightfield dye on the non-neuroendocrine tumor sample.

17. 17. The method of claim 16, wherein the secondary antibody is haptenized and the tertiary antibody is an anti-hapten antibody.

18. 10. A method for selecting a patient for a Trk-directed therapy, comprising detecting the presence of a Trk fusion protein in the non-neuroendocrine tumor sample according to the method of claim 1, and providing the result of the detection as an indicator for selecting the patient for the therapy, where the non-neuroendocrine tumor sample scores as positive for a fusion protein involving TrkA, TrkB, or TrkC.

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