Exploring the Molecular Mechanism Based on KIT Mutation

Launched by XIJING HOSPITAL · Jun 8, 2023

Keywords

ClinConnect Summary

This clinical trial is exploring how certain gut bacteria might influence the treatment of gastrointestinal stromal tumors (GIST) in patients who have genetic mutations called KIT mutations. Researchers want to understand if the gut microbiota, which is the community of bacteria in our intestines, can affect how well a medication called imatinib works for patients with GIST that cannot be surgically removed or has come back after treatment. The goal is to find out if the composition of gut bacteria could help predict how effective the treatment will be and if adjusting these bacteria might improve therapy outcomes.

To participate in this study, individuals must be between 18 and 74 years old, have a specific body mass index (BMI), and have been diagnosed with an unresectable GIST that shows the KIT mutation. They should not have had any prior surgeries or significant health issues that could complicate their participation. Participants will undergo tests to ensure their organ functions are stable and will be closely monitored throughout the trial. This study aims to provide personalized treatment options for patients with advanced GIST by incorporating an understanding of their gut health.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • BMI index 18.5-23.9kg/m2;
• • Pathologically diagnosed patients with unresectable GIST, and genetic testing is C-kit9/11 mutation;
• • No previous surgery;
• • ECOG score: 0-1 points;
• • Expected survival period ≥ 6 months;
• • All patients should have measurable or evaluable target lesions;
• • Able to eat liquid diet The above; no complete gastrointestinal obstruction or perforation; no distant metastasis;
• * The main organ functions are normal, that is, the following criteria are met:
• • 1. The blood routine examination standards must be met (no blood transfusion and blood products within 14 days, no G-CSF use) and other hematopoietic stimulating factors): a) HB≥80 g/L; b) ANC≥1.5×109/L; c) PLT≥100×109/L;
• • 2. Biochemical tests should meet the following criteria: a) TBIL \<1.5×ULN; b) ALT and AST\<2.0×ULN; c) Serum Cr≤1.5×ULN or endogenous creatinine clearance rate\> 50 mL/min (Cockcroft-Gault formula);
• • 3. Pulmonary function assessment of normal lung function or mild to moderate abnormality (VC%\>60%, FEV1\>1.2L, FEV1%\>40%, DLco\>40%);
• • 4. Cardiovascular function evaluation: cardiac function grades I to II;
• • Have certain self-care Ability and language comprehension.
• Exclusion Criteria:
• • 1. Patients with pathological types and primary tumor sites that do not meet the inclusion criteria;
• • 2. There is a risk of gastrointestinal perforation;
• • 3. Has undergone surgical treatment;
• • 4. Have ever suffered from malignant tumor;
• • 5. Those with a history of severe lung or heart disease;
• • 6. Active infection or unexplained fever \>38.5℃ within 2 weeks before randomization;
• • 7. Known major active infection, or the investigator judges that there is a major blood, renal, metabolic, gastrointestinal or endocrine dysfunction;
• • 8. Those with a history of immunodeficiency, including HIV positive or other acquired or congenital immunodeficiency diseases, or a history of organ transplantation;
• • 9. The subject has active hepatitis B (HBV DNA ≥ 2000 IU/mL or 104 copies/mL), hepatitis C (positive hepatitis C antibody, and HCV-RNA is higher than the detection limit of the analytical method);
• • 10. Those who have been vaccinated with live vaccines within 3 months before treatment;
• • 11. During acute or chronic tuberculosis infection (positive T-spot test and suspected tuberculosis foci on chest X-ray);
• • 12. Those with a history of drug, drug or alcohol abuse (drinking ≥5 times a week, etc.);
• • 13. Intravenous infusion cannot be performed;
• • 14. Severe diarrhea in the past 2 months (watery stools ≥ 3 times per day and lasted ≥ 3 days);
• • 15. Severe constipation (≤2 times of defecation per week with difficulty in defecation) in the past 2 months;
• • 16. Antibiotics have been used in the past 2 months for 3 days or more;
• • 17. Have used proton pump gastric drugs, acid suppressants, mucosal protective agents, opioid psychotropic drugs, hormones, immunosuppressants, cytotoxic drugs and other drugs within the past 2 months for 3 days or more;
• • 18. Have used probiotics, prebiotics or synbiotic within the past 2 months for 3 days or more;
• • 19. Received drug treatment for the following diseases in the past 1 month: cholecystitis, peptic ulcer, urinary tract infection, acute pyelonephritis, cystitis, hyperthyroidism and other abnormal thyroid function;
• • 20. Gastrointestinal surgery, appendicitis surgery, enema, colon cleansing and other medical operations within the past 1 year;
• • 21. During pregnancy and lactation (women) or lactose intolerance;
• • 22. Patients with high blood pressure that cannot be reduced to the normal range after antihypertensive drug treatment (systolic blood pressure\>140 mmHg, diastolic blood pressure\>90 mmHg); patients with a history of unstable angina pectoris; newly diagnosed within 3 months before screening Angina pectoris or myocardial infarction within 6 months before screening; arrhythmia (including QTcF: ≥450 ms for men, ≥470 ms for women) requires long-term use of antiarrhythmic drugs and New York Heart Association classification ≥ grade II cardiac insufficiency;
• • 23. According to the judgment of the investigator, the subject has other factors that may cause him to be forced to terminate the study halfway, such as suffering from other serious diseases (including mental illness) requiring combined treatment, serious abnormal laboratory test values, family or social factors, Situations that may affect the safety of subjects or the collection of trial data;
• • 24. The investigator judges other circumstances that may affect the conduct of clinical research and the judgment of research results;
• • 25. Research center staff, researcher's partner or first-degree relative;