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Construction method and application of prediction model for non-small cell lung cancer immune checkpoint inhibition treatment effect based on organ metastasis spectrum

A non-small cell lung cancer, immune checkpoint technology, applied in the field of biomedicine, can solve the problems of lack of comprehensive analysis, inability to distinguish immunotherapy-specific prediction, limited clinical significance, etc., to achieve the effect of improving understanding

Active Publication Date: 2021-09-17
NANFANG HOSPITAL OF SOUTHERN MEDICAL UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, these studies were all performed in the single-arm setting of ICI, lacking a control group of conventional treatment (e.g. chemotherapy) for comparison, resulting in the inability to distinguish between immunotherapy-specific predictions and treatment-independent prognostic effects
Furthermore, previous studies of the effect of treatment on each metastatic organ have been isolated, thus lacking a comprehensive analysis that looks at the big picture and encompasses the entire metastatic landscape; Clinical significance of outcome studies in single metastatic organs is limited

Method used

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  • Construction method and application of prediction model for non-small cell lung cancer immune checkpoint inhibition treatment effect based on organ metastasis spectrum
  • Construction method and application of prediction model for non-small cell lung cancer immune checkpoint inhibition treatment effect based on organ metastasis spectrum
  • Construction method and application of prediction model for non-small cell lung cancer immune checkpoint inhibition treatment effect based on organ metastasis spectrum

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Experimental program
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Effect test

Embodiment 1

[0039] A method for constructing a predictive model for the outcome of non-small cell lung cancer immune checkpoint inhibition therapy

[0040] A total of 2062 patients with advanced NSCLC treated with ICIs were selected, including 850 patients from the OAK phase III trial (OAK cohort), 136 patients from the FIR phase II trial (FIR cohort), and 667 patients from the BIRCH phase II trial (BIRCH cohort). ) and 409 patients in Nanfang Hospital of Southern Medical University (NFyy-ICI cohort), conducted in accordance with Roche’s policies and procedures for clinical research data sharing and approval by the Institutional Ethics Review Board of Nanfang Hospital, patients in the OAK cohort were assigned to atezolizumab Antibody group and docetaxel group, FIR cohort and BIRCH cohort were atezolizumab group screened by PD-L1, and NFyy-ICI cohort used at least one dose of ICI as first-line or follow-up treatment.

[0041] The baseline PD-L1 status of the three cohorts (OAK, FIR, BIRCH)...

Embodiment 2

[0076] Validation and comparison of predictive models

[0077] (1) METscore can identify the beneficiaries of immune checkpoint inhibition therapy

[0078] First, the METscore system was validated in a PD-L1 selected OAK cohort, two single-arm clinical cohorts (FIR and BIRCH), and a real-world cohort (NFyy-ICI) cohort.

[0079] To this end, the Kaplan-Meier curves of OS with different METscores in the PD-L1 positive population based on OAK, FIR, BIRCH, and NFyy-ICI were drawn, as shown in Figure 8 As shown, where A is the Kaplan-Meier curve of OS with different METscore in the atezolizumab group of the OAK cohort, B is the Kaplan-Meier curve of OS with different METscores in the docetaxel group of the OAK cohort, and C is the OS of the FIR cohort The Kaplan-Meier curve of OS with different METscore in the atezolizumab group, D is the Kaplan-Meier curve of the OS with different METscore in the atezolizumab group in the BIRCH cohort, E is the atezolizumab group in the NFyy-ICI...

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Abstract

The invention relates to the field of biomedicine, in particular to a construction method and application of a prediction model for non-small cell lung cancer immune checkpoint inhibition treatment effect based on organ metastasis spectrum. The construction method comprises the following steps: evaluating and comparing the influence of different baseline transfer organs in an OAK queue on OS and PFS of patients in an attezumab group and a docetaxel group, the prediction effect of the transfer organ spectrum of different PD-L1 expression level stratification of the atezumab group and docetaxel group in OAK queue, and OS of different transfer organ types and numbers of the attezumab group and the docetaxel group in a PD-L1 positive OAK queue; establishing a scoring system METscore based on the organ transfer spectrum, performing multivariable Cox proportional risk regression, and predicting a clinical result of ICI treatment by calculating a total score of a prognosis effect and a prediction effect. Immunotherapy prediction and prognosis effects of the metastatic organ spectrum of the advanced NSCLC patient are described, clinical decisions of tumor immunotherapy patients are facilitated, and understanding of metastatic organ specificity anti-tumor immunity is improved.

Description

technical field [0001] The invention relates to the field of biomedicine, in particular to a method for constructing a predictive model for the curative effect of non-small cell lung cancer immune checkpoint inhibition therapy based on an organ metastasis profile and its application. Background technique [0002] Immune checkpoint inhibitors (ICIs), represented by programmed cell death protein-1 (PD-1) or programmed cell death ligand 1 (PD-L1) monoclonal antibodies, have changed the treatment paradigm as advanced or metastatic mainstay of treatment for non-small cell lung cancer (NSCLC). Despite the success of immunotherapy relative to chemotherapy over the past decade, PD-(L)1 blockade has fallen far short of inducing durable immune responses, even in PD-L1-positive populations, there is an urgent need for reliable predictors of immunotherapy to facilitate precision medicine. [0003] The effectiveness of ICI therapy is related to the biological properties of the tumor mi...

Claims

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Application Information

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IPC IPC(8): G16H50/70G16H20/10G16H70/40
CPCG16H50/70G16H20/10G16H70/40
Inventor 董忠谊吴德华马思聪白雪林彦
Owner NANFANG HOSPITAL OF SOUTHERN MEDICAL UNIV
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