Study of Sirolimus in Patients With Advanced Pancreatic Cancer

1. Research purpose This clinical trial was designed to evaluate the anti-tumor effect of sirolimus in patients with advanced or postoperative recurrent pancreatic cancer with second-line standard therapy resistance. 2. Grouping and sample size calculation A single-arm study was designed. Based on clinical experience and literature, the expected median survival period of patients with advanced pancreatic cancer after second-line resistance or postoperative recurrence was about 3 months, and the median survival period of such patients was expected to be extended to 6 months after the treatment with sirolimus. The significance level of statistical test was set at 0.05 and the power of test was set as 80%, the time of enrollment was set to June 2021, and the time of follow-up was set to June 2023. The follow up loss rate was predicted as 5%, and the number of cases needed to be enrolled was calculated as 36. 3. Clinical trial procedure For the cases to be included, the patient's medical history, symptoms, signs and other conditions should be examined in advance, informed consent should be obtained and signed, and the patient's age, height, weight, medical history, symptoms, signs, pathological results, tumor node metastasis (TNM) stage and other contents should be recorded.According to the test requirements, the study was designed to be limited to 5 years, and the day of oral administration of sirolimus will be set as the first day, tumor markers will be follow up every 3 weeks.Each 3-month review includes symptoms, signs, adverse events, blood routine examination, liver and kidney function, abdominal enhanced CT, liver enhanced MRI+ diffusion, and chest high-resolution CT. Overall survival (OS) was taken as the primary endpoint and then recorded to the secondary endpoint. All results were recorded in the case report form, clinical efficacy and safety were evaluated, and adverse events were observed.If the patient cannot come to the hospital for reexamination, follow up will be conducted by telephone, email, etc. 4. Adverse events record and report Information on non-serious adverse events that occur during treatment should be recorded on the clinical trial report form (CRF), and all serious adverse events will be recorded in the CRF report form.Few patients in this study may have serious liver and kidney function injury, may have allergy reaction, secondary hypertension, hypercholesterolemia, serious infection and so on. In view of the above possible situations, investigators will fully evaluate the liver and kidney function before treatment, and give protective drugs for organ function; And the corresponding adjuvant drugs such as blood pressure drugs, lipid-regulating drugs to prevent sirolimus side effects;The symptoms and indicators of infection were closely monitored. Once adverse events happen, report will be sent to the general manager and the head of the hospital immediately, and also to the ethics committee of adverse events within the specified time, and make unified analysis after the study. 5. Data management and statistical analysis Data recording and auditing: The observation data will be recorded by the attending physician in the case report form, and the data records shall be timely, complete, accurate and authentic.The form will be filled out in black (or blue and black), any changes will be made by the relevant personnel, and then signed and dated. The changes will not cover the original record. If possible, copy the relevant test paper and paste it on the attached page after CRF. Data entry: Establish data entry program and database for statistical analysis. 6. Informed consent The subject must obtain written informed consent before performing the study procedures to inform the patient of the specific content related to the study. The specific procedures for obtaining informed consent include: the patient's disease characteristics, treatment plan and related risks shall be informed in detail by the competent doctor, and the patient or legal guardian with civil capacity shall sign the informed consent after fully knowing and understanding the relevant process and risks of this study.