PLATFORM Study of Precision Medicine for Rare Tumors

Inclusion Criteria

• •1. Male or female, the age at the time of signing the informed consent is no less than 18 years old;
• •2. Patients with advanced or metastatic rare solid tumor confirmed by histological confirmed;
• •3. ECOG score is 0 or 1; ECOG score needs to be evaluated 7 days before the first treatment;
• •4. Expected survival ≥12 weeks;
• •5. According to Response Evaluation Criteria in Solid Tumor (RECIST 1.1), there is at least one imaging measurable lesions, which has obvious disease progress before radiotherapy or after radiotherapy;
• •6. Within the scope of CMPA approved drug indications, the disease has progressed after the standard treatment recommended by NCCN or CSCO guidelines (if there is standard treatment, the recommended level is IA-IIA), or there is no standard effective treatment plan, or it is no longer suitable for standard anti-tumor treatment, or the patients refuse the standard treatment plan;
• •7. Fresh biopsy tissue samples (obtained within 12 weeks before the first use of the drug, 4 pieces of coarse needle biopsy must be provided, and no other anti-tumor treatment, systemic anti infection treatment, vaccination, et al.) and peripheral blood samples must be provided for molecular typing;
• •8. Must have a primary or metastatic paraffin specimen (without radiotherapy) other than bone metastatic lesions before enrollment (within 2 years, 15-20 sheets, 4-6μm thick white slices, of which 5 need to be glued and baked ). If requirements are not met, investigator are allowed the decision to enroll subjects according to the specific situation.
• •9. If there is pleural or peritoneal effusion, the specimens must be taken for pathological cytological examination of which 300 ml samples must be provided;
• •8. Major surgical operations or incomplete healing of injury within 28 days prior to study treatment's first administration and chest radiotherapy of \> 30 Gy within 6 months.
• •9. History of receiving other investigational drugs within 14 days or 5 half-lives (whichever is longer) prior to the first administration.
• •10. History of receiving live vaccine within 30 days prior to the first administration. Seasonal influenza vaccines that do not contain live viruses are allowed.
• •11. History of hypersensitivity to the active ingredients or non-active excipients of the study drug, hypersensitivity to drugs with chemical structure similar to the study drug or hypersensitivity to similar drugs of the study drug.
• •12. Current active infection requiring systemic treatment (antibiotics); or any of the following:
• •1. HIV positive or known history of acquired immunodeficiency syndrome;
• •2. Hepatitis B virus (HBV) or hepatitis C virus (HCV) infection is defined as HBsAg positive and the number of HBV DNA copies exceeds the upper limit of normal value, or HCV AB positive;
• •3. Active tuberculosis (with exposure history or positive tuberculosis test; with clinical and / or imaging manifestations);
• •4. Positive antibody of Treponema Pallidum.
• •13. Current evidenced uncontrollable systemic diseases (such as severe mental, neurological, epilepsy or dementia, unstable or uncompensated respiratory, cardiovascular, liver or kidney diseases, uncontrolled hypertension \[i.e., still greater than or equal to CTCAE Grade 3 hypertension after drug treatment\]).
• •14. History of myocardial infarction, coronary artery / peripheral artery bypass or cerebrovascular accident within 3 months.
• •15. Diagnosed with a second type of malignant tumor within 5 years before the first diagnosis of a rare solid tumor (excluding completely resected basal cell carcinoma, bladder carcinoma in situ, cervical carcinoma in situ).
• •16. History of receiving of any organ transplantation, including allogeneic stem cell transplantation. Transplantation without immunosuppression (corneal transplantation, hair transplantation) is excluded.
• •17. Cardiovascular disease or symptom includes any of the following:
• •1. History of Congestive Heart Failure requiring treatment and of New York Heart Association class III / IV CHF (see Appendix 3) ;
• •2. Current ventricular arrhythmia requiring antiarrhythmic drugs treatment, or uncontrollable or unstable arrhythmia;
• •3. Severe conduction disorder (such as grade II or III AV block);
• •4. Angina requiring treatment;
• •5. QT interval (QTC) of 12 lead ECG is ≥ 450 ms in male and ≥ 470 MS in female;
• •6. History of congenital long QT syndrome, congenital short QT syndrome, torsade de pointe or pre-excitation syndrome;
• •7. History of LVEF decline to below 50% determined by echocardiography or MUGA scan;
• •8. History of myocardial infarction in the past 6 months.
• •18. Inadequate bone marrow reserve or organ function evidenced by the following laboratory results:
• •1. Absolute value of neutrophils \< 1.5 × 109 / L;
• •2. Platelet count \< 100 × 109 / L (transfusion dependent patients should be excluded from this study);
• •3. Hemoglobin \< 90g / L;
• •4. ALT is \> 2.5 x Upper Limit of Normal (ULN) If there is no clear liver metastases, ALT \> 5 x ULN if there is liver metastases;
• •5. Aspartate aminotransferase (AST) \> 2.5 x ULN If there is no definite liver metastases. AST \> 5x ULN if there is liver metastases;
• •6. Total bilirubin \> 1.5 x ULN if there is no liver metastases; Total bilirubin \> 3 x ULN if there is definite Gilbert syndrome (Unconjugated Hyperbilirubinemia) or liver metastases;
• •7. Creatinine \> 1.5 x ULN with Creatinine clearance \< 50 ml / min (measured value, or calculated value by Cockcroft Gault formula); Only when Creatinine \> 1.5 x ULN, Creatinine clearance needs to be checked for confirmation;
• •8. If bone metastasis is present and investigator concluded that liver function is adequate, the increase of ALP alone will not be excluded;
• •9. Coagulation function: INR, PT, APTT\> 1.5 times ULN (whether the patients using or not using anticoagulant drugs can be enrolled is determined by the investigator).
• •10. Myocardial enzyme CK and CKMB test values are not in the normal range;
• •11. The examination value of thyroid function is not within the normal range or it is not slightly abnormal but does not need treatment.
• •19. History of swallowing dysfunction, active gastrointestinal disease or other diseases that significantly affect the absorption, distribution, metabolism and excretion of oral drugs. The patients with history of subtotal gastrectomy. (Note: this standard is not applicable to the sub schemes with the investigational drug as injection).
• •20. Pregnant or lactating women.
• •21. Serious medical or mental illness that may affect program compliance and tolerance to treatment.
• •22. Those investigators believe that patients with other potential risks are not suitable for this study.