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临床试验/NCT07665736
NCT07665736尚未招募不适用

Real-world Study on the Efficacy, Safety, and Prognostic Factors of Immune Checkpoint Inhibitors Combined With Radiotherapy in Patients With Malignant Tumors: A Prospective Non-interventional Clinical Study

Sichuan University1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2026年6月30日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
200
试验地点
1

研究概览

简要总结

Currently, chemotherapy, targeted therapy, immunotherapy, and radiotherapy are the core treatment modalities for malignant tumors, with technologies advancing rapidly. Radiotherapy can induce massive tumor cell death in a short period and expose abundant tumor-specific antigens, turning the irradiated tumor into an endogenous tumor vaccine and even causing regression or disappearance of non-irradiated tumors (the abscopal effect) . Preclinical studies have shown that stereotactic body radiotherapy (SBRT) combined with PD-1/PD-L1 inhibitors can activate systemic immunity, sensitize tumor-specific T cells to enter the bloodstream, and enable their homing to distant tumors, thereby inhibiting the growth of non-irradiated tumors . However, conclusions from rigorous randomized controlled trials have limitations when applied to the complex and heterogeneous patient populations in real-world settings. Real-world research is increasingly valued globally to complement traditional clinical trial evidence. This project prospectively collects data from patients receiving immunotherapy combined with radiotherapy in real-world clinical practice, which is of great value for evaluating long-term efficacy, safety, and impact on quality of life, and can provide high-level evidence for optimizing clinical practice and informing healthcare decisions.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years;
  • Histologically or cytologically confirmed malignant tumor;
  • Planned to receive immunotherapy combined with radiotherapy as the basis of treatment;
  • At least one measurable lesion according to the Response Evaluation Criteria in Solid Tumors (RECIST 1.1);
  • Adequate organ function (reference may be made to laboratory test indicators, such as routine blood tests, liver and kidney function);
  • Voluntarily participate in this study, sign the informed consent form, and agree to comply with follow-up.

排除标准

  • Patients with severe cognitive impairment, mental illness, or other conditions that, in the judgment of the investigator, preclude them from cooperating with participation in this study;
  • Active, uncontrolled serious infection, or known human immunodeficiency virus (HIV) infection;
  • Pregnant or breastfeeding women;
  • Any unstable systemic disease (including but not limited to severe cardiac, hepatic, or renal insufficiency).

研究者

发起方
Sichuan University
申办方类型
Other
责任方
Principal Investigator
主要研究者

You Lu

MD. PhD

Sichuan University

研究点 (1)

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