56 results about "Pre-Therapy" patented technology

A medical digital expert system to predict a patient's response to a variety of treatments (using pre-treatment information) is described. The system utilizes data fusion, advanced signal / information processing and machine learning / inference methodologies and technologies to integrate and explore diverse sets of attributes, parameters and information that are available to select the optimal treatment choice for an individual or for a subset of individuals suffering from any illness or disease including psychiatric, mental or neurological disorders and illnesses. The methodology and system can also be used to determine or confirm medical diagnosis, estimate the level, index, severity or critical medical parameters of the illness or condition, or provide a list of likely diagnoses for an individual suffering / experiencing any illness, disorder or condition.

The present invention provides novel methods of inhibiting fibrosis, as well as methods of treating or inhibiting fibrotic disorders, using BMP9 and / or BMP10 antagonists. The present invention also provides methods of assessing whether a subject has or is at risk of developing a fibrotic disorder by detecting levels of BMP9 and / or BMP10. Further provided are methods of assessing the efficacy of a treatment regimen for treating a fibrotic disorder by detecting and comparing pre-treatment levels of BMP9 and BMP10 with post-treatment levels of BMP9 and BMP10.

The present invention discloses an enhancement agent for high intensity focused ultrasound (HIFU) treatment, which is administered to a patient before HIFU treatment and can reduce the level of EEF at the target location to be treated with HIFU. EEF is presented by the expression: EEF=ηPt / V (unit: J / mm3), and refers to the HIFU energy needed to effectively treat a tumor per unit volume of the tumor, wherein, η=0.7; P refers to the total acoustic power of HIFU source (unit: W); t refers to the total time of HIFU treatment (unit: s); V refers to the volume of HIFU-induced lesions (unit: mm3). If the amount of EEF at the target location before administration of the enhancement agent is defined as EEF(base) and the amount of EEF at the target location after administration of the enhancement agent is defined as EEF(measurement), the ratio between EEF(base) and EEF(measurement) is more than 1, preferably more than 2, and more preferably over 4. The use of the enhancement agent for HIFU treatment of the present invention makes it possible to treat deep-seated tumors. In addition, patients with hepatic tumors can be effectively treated without removal of ribs. Accordingly, the present invention discloses methods for increasing acoustic energy deposition at target location during HIFU treatment and screening the enhancement agents for HIFU treatment.

Described herein is a method of improving seizure control in a patient experiencing uncontrolled seizures persisting 10 minutes or more, comprising administering fenfluramine or a pharmaceutically acceptable salt, base, acid or amine thereof, at a dose of from 0.2 to 1.2 m / kg / day for a period of about 12 hours to about 7 days to a patient having been put into a therapeutic, medically-induced coma via a general anesthetic; and after about 12 hours to about 7 days, weaning the patient from the general anesthetic and assessing whether the seizure control has improved as compared to a pre-treatment time point. The patient experiencing seizures may have epilepsy or epileptic encephalopathy that has led to established status epilepticus (SE), refractory status epilepticus (RSE) or super-refractory status epilepticus (SRSE).

The invention relates to an in-situ bladder cancer animal model. An establishment method of the animal model comprises the step of perfusing 20mg / mL carcinogen MNU solution in a bladder of an SD rat to cause the bladder cancer, wherein 0.1mL of carcinogen MNU solution is perfused per time per week, and six times in total. The in-situ bladder cancer animal model has the advantages that the novel establishment method is provided for the in-situ bladder cancer animal model; a novel method for establishing the model of detecting the bladder cancer through a living body is provided, so that a tumour model not beneficial to further in vivo experiment can be removed, and meanwhile, the effect of pretherapy and post-treatment of the bladder caner animal model can be evaluated by utilizing CT (Computed Tomography) scanning; the method for diagnosing the in-situ bladder cancer of the rat through CT scanning is more sensitive, higher in accuracy, and more direct and convenient, and can provide convenience for further experiment research of the animal model.

Methods, compositions, and kits for identifying individuals who will be responsive to post-operative radiation therapy for treatment of prostate cancer are disclosed. In particular, the invention relates to a genomic signature based on expression levels of DNA Damage Repair genes that can be used to identify individuals likely to benefit from post-operative radiation therapy after a prostatectomy.

A beam irradiation target verification apparatus (1) includes an X-ray switching emission process unit (6a) that causes a vertical X-ray emitting unit (13) to emit at least two types of X-rays using an energy-level switching unit (11), a vertical X-ray detection unit (14) that detects an X-ray emitted from the vertical X-ray emitting unit (13), a pre-therapy verification image generation process unit (7) that generates pre-therapy verification images (20B) and (20C) based on detection information on at least two types of X-rays obtained by the vertical X-ray detection unit (14), a reference image acquisition unit (3) that acquires a reference image (20A) obtained at a therapy planning stage, a comparison process unit (8a) that makes comparisons between the pre-therapy verification images (20B) and (20C) and the reference image (20A), and a result output unit (4) that outputs a comparison result obtained by the comparison process unit (8a). Thus, there is provided a beam irradiation target verification apparatus for therapeutic purposes capable of measuring internal conditions of a therapy patient and determining necessity of changing a therapy plan, easily and at a relatively low exposure level.

The present invention relates to protein kinase A (PKA) for use in diagnosing autism spectrum disorder (ASD) phenotype 1 in an ASD patient wherein PKA levels are measured in a sample of the patient and wherein ASD phenotype 1 is diagnosed if the measured levels are lower than PKA levels in an age and sex-matched control sample. Additionally, the present invention relates to PKA for use in monitoring variation in ASD severity in an ASD patient, wherein PKA levels are measured in a sample of the patient and an increase in ASD severity is characterized by a decrease of PKA levels compared to PKA levels measured in previous samples of the patient. The present invention also relates to PKA for use in monitoring efficacy of an ASD treatment in an ASD phenotype 1 patient, wherein PKA levels are measured in a sample of the patient and wherein a positive response to the ASD treatment is characterized by an increase of PKA levels in comparison to baseline PKA levels of the patient prior to treatment. Furthermore, the present invention is directed to methods of diagnosing ASD phenotype 1 as well as kits comprising means to measure PKA levels.

Glycosylation modification in serum of an ovarian cancer patient before treatment is detected, and the sensitivity of the ovarian cancer patient to platinum chemotherapeutic drugs is subjected to prognosis evaluation by combining alpha 2, 3 sialic acid N-sugar chains with CA125. A detection object of the kit is serum of an ovarian cancer patient before treatment; the method comprises the followingsteps: detecting serum glycosylation modification by using an analytical instrument, calculating the relative expression quantity of alpha 2, 3 sialic acid type N-sugar chains, and performing binarylogistic regression analysis in combination with the content of CA125 in serum of a patient by using SPSS software to obtain a prediction probability; taking 0.24 as a critical value, if the prediction probability is greater than 0.24, determining that the patient is a drug-resistant patient, and if the prediction probability is less than 0.24, determining that the patient is a sensitive patient.The method has the advantages that the chemotherapy effect of the medicine on the patient is predicted by utilizing the proper marker, a treatment scheme more suitable for the patient is selected, andthe survival rate of the ovarian cancer patient is further improved.

The present invention provides a method for predicting a therapeutic effect and / or monitoring recurrence in a cancer patient. Disclosed is a method for detecting a therapeutic effect of cancer treatment in a cancer patient, comprising: measuring nematode tactic behavior to each of pre-treatment urine and in-treatment or post-treatment urine from the cancer patient; and comparing a result of measuring the tactic behavior to the pre-treatment urine and a result of measuring the tactic behavior to the in-treatment or post-treatment urine, wherein when attraction is weakened or avoidance is strengthened after the treatment, it is determined that the therapeutic effect is detected.

The invention discloses an adjuvant for high-intensity focusing and ultrasonic (HIFU) treatment, which can be used for lowering the EEF of the HIFU therapeutic target region for the patients, the adjuvant makes it possible to carry out HIFU treatment during deep layer tumor treatment without the requirement of ablation of the patients' rib. The invention also provides a method for increasing target region energy deposition and screening HIFU adjuvant in HIFU treatment.

The invention belongs to the technical field of medical biology, and particularly discloses a kit for predicting prognosis of drug-loaded microsphere chemoembolization treatment of liver cancer, and the kit comprises reagents and / or instruments for detecting the alpha fetoprotein expression quantity, ALRI, the tumor diameter, Child-Pugh grading, proportion of tumor in liver, a portal vein invasion state and a tumor remote metastasis state. The kit disclosed by the invention can be used for predicting the lifetime of the liver cancer patient after DEB-TACE treatment according to clinical indexes of the liver cancer patient before DEB-TACE treatment and evaluating DEB-TACE treatment prognosis of the liver cancer patient, so that an interventional doctor can screen patient crowds suitable for DEB-TACE treatment before an operation; and clinical doctors can accurately evaluate the prognosis of the patient conveniently, and an individualized follow-up visit scheme can be made according to the expected lifetime.

An apparatus, method, system, computer-readable medium and use for individual patient therapy planning of diseases such as cancer for different therapy modalities, such as radiation therapy and chemotherapy is provided. A new aspect of the invention is that the degree of bone marrow depression of the patient is related to the count of immature blood platelets, which are measured before each treatment. Some embodiments of the invention provide an advantage allowing reducing the level of uncertainty in the prediction of the risk of bone marrow depression, and thus enabling to safely improve the therapy effect by an increase of the radiation dosage and / or chemical dosage to the individual patient while the risk for bone marrow depression is minimized.

The invention discloses a tumor immune cell therapy platform. Tumor immune cell therapy can be standardized through the following steps: one, the establishing of immune function test items; two, the establishing of test specification technologies; three, the training of medical staff and laboratory staff; four, the establishing of a standardized management system; five, the controlling of quality;and six, the establishing of a clinical grade CAR-T cell preparation technology platform; through the building of the platform, tumor treatment can be more standardized, and the probability of errorduring treatment can be reduced; and the monitoring before and after treatment can be performed on the immune cells and cytokines of patients, and therefore, the platform has important clinical significance in preventing CRS.

Cancer immunotherapy has obtained a huge clinical success, and even the most difficult-to-treat cancer also has a relatively long lifetime. However, this effect is observed only in a small number of persons and no biomarkers of this reaction. The methods described herein use two independent systemic chronic inflammation metrics (inflammation age-iAge-and cytokine response score-CRS) to stratify cancer patients into responders and non-responders to cancer immunotherapy, thereby improving the outcome of cancer immunotherapy. The iAge personalized immunoproteomic markers / features create an individualized initial therapy to reduce the iAge and convert unresponsive patients to reactants prior to treatment. By treating a patient to reduce its iAge and improve its CRS, unresponsive persons can be converted into reactants.

The invention discloses a detection method for colorectal cancer polygene ctDNA, which specifically comprises the following steps: S1, collecting a pre-treatment tissue specimen; S2, treating a blood sample; S3, performing cfDNA extraction; S4, measuring the concentration and detecting the size of a fragment; S5, performing mixing and centrifuging; S6, performing a ddPCR detection stage; S7, reading a fluorescence signal; and S8, analyzing a numerical result. The invention relates to the technical field of molecular diagnosis gene detection. According to the detection method for the colorectal cancer polygene ctDNA, ddPCR amplification is performed on cfDNA through a specific detection primer and a probe of a reference gene beta-Actin; an amplification product is detected; finally, fluorescence signal data is analyzed; fluorescence information of KRAS, NRAS, PIK3CA and BRAF genes and the reference gene beta-Actin is obtained; plasma ctDNA possibly replaces tumour tissue biopsy; and as a molecular marker for auxiliary diagnosis of colorectal cancer, change of RAS (KRAS, NRAS), BRAF and PIK3CA gene mutation states in ctDNA of a patient before and during cetuximab treatment is dynamically monitored.

The invention discloses a polymolecular marker and a device for clinically evaluating the sensitivity of ulcerative colitis patients to golimumab, wherein the polymolecular marker comprises CPB1, IL1B and / or SRGN, and the accuracy of predicting the sensitivity of the ulcerative colitis patients to the golimumab is high; and the polymolecular marker can be used for monitoring the sensitivity of the ulcerative colitis patients to golimumab in real time before and after treatment, so that clinical doctors can conveniently adopt personalized treatment schemes in time, and blind medication is avoided.

The invention belongs to the biotechnical field, and concretely relates to a new prostate cancer molecule marker microRNA 135a-3p (MIR135a-3p) and a use thereof in the preparation of preparations for diagnosing and treating the prostate cancer. The use comprises the following steps: screening prostate cancer high-risk populations, diagnosing the prostate cancer, designing prostate cancer drug target, monitoring the prostate cancer treatment condition, and carrying out prognosis detection on the prostate cancer. A method using the molecule marker and a diagnostic kit containing the molecule marker to diagnose the prostate cancer has the characteristics of simplicity in operation, convenience in material drawing, good safety, no wounds, high specificity, high sensitivity, and easiness in massive screening.

Provided is a method comprising recommending treatment of a prostate cancer patient with a polo-like kinase-1 (PLK1) inhibitor if the patient has rising prostate specific antigen (PSA) levels.Also provided is a method comprisingmeasuring prostate specific antigen (PSA) levels in at least two samples from a prostate cancer patient, the samples obtained from the patient at different times; andrecommending treatment of the patient with a PLK1 inhibitor if the PSA levels in the samples increase over time, ornot recommending treatment of the patient with a PLK1 inhibitor if the PSA levels in the samples do not increase over time.Additionally provided is a method comprising recommending treatment of a PLK1 inhibitor to a patient having a prostate cancer that has an altered androgen receptor that does not require ligand for activation.

Provided herein are drug implants comprising a therapeutically active agent for the treatment of disease in a subject. In some cases, the drug implant may comprise a polymer matrix and a therapeutically active agent disposed therein. Additionally provided are methods for manufacturing the drug implants and methods of treating diseases with the implants. In some cases, the drug implant may comprise bicalutamide, e.g., for use in the treatment of prostate cancer.