LDRT Combined With Pucotenlimab and Standard Therapy for Advanced Pancreatic Cancer: A Sin
To investigate the activating effect of local lesion low-dose radiotherapy (2Gy) on the tumor immune microenvironment, and the efficacy, safety, and feasibility of its combination with pembrolizumab and standard therapy in patients with advanced pancreatic cancer. Concurrently, to preliminarily establish an efficacy pr
| Condition(s) | Pancreatic Cancer, PD-L1, PD-1 Inhibitor, LDRT, Proterizumab |
|---|---|
| Status | Recruiting |
| Phase | Phase 1, Phase 2 |
| Study type | Interventional |
| Summary | To investigate the activating effect of local lesion low-dose radiotherapy (2Gy) on the tumor immune microenvironment, and the efficacy, safety, and feasibility of its combination with pembrolizumab and standard therapy in patients with advanced pancreatic cancer. Concurrently, to preliminarily establish an efficacy prediction model for the early identification of patient populations who would benefit from the treatment, thereby providing a theoretical foundation for the implementation of precision medicine. |
| Who can participate | Inclusion Criteria: * Age ≥ 18 years, regardless of gender; * ECOG score of 0 to 1; * Patients with histologically or cytologically confirmed pancreatic malignancy; * No prior treatment with PD-1 or PD-L1 inhibitors; * Presence of a radiotherapeutically eligible target lesion (excluding bone metastases); * Subjects voluntarily participate in the study and provide signed informed consent. Exclusion Criteria: * Previous history of radiotherapy; * Uncontrolled chronic infectious or non-infectious diseases, including but not limited to: medication-refractory heart failure, poorly controlled hypertension, etc.; * Active or clinically uncontrolled severe infections; * History of psychoactive drug abuse that cannot be abstained from, or patients with psychiatric disorders; * Pregnant or lactating |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Lead sponsor | Zhejiang Provincial People's Hospital |
| Locations | Hangzhou, Zhejiang, China |
| Start date | 2025-09-30 |
| NCT ID | NCT07312422 |
| Official listing | https://clinicaltrials.gov/study/NCT07312422 |