Phase I/II Clinical Study of PRaG Regimen Combined With Intraperitoneal Infusion of PD-1 Inhibitor for Advanced Refractory Solid Tumors With Cancerous Ascites (PRaG4.0P Study)

Author:

Xu Yingying1234,Kong Yuehong1234,Ma Yifu1234,Xu Meiling1234,Yang Jiabao1234,Zhang Junjun1234,Chen Rongzheng1234,Chen Guangqiang5,Hong Zhihui6,Zhao Xiangrong1234,Zhang Chenyang1234,Xing Pengfei1234,Zhang Liyuan1234,Zhao Peifeng1234ORCID

Affiliation:

1. Center for Cancer Diagnosis and Treatment, The Second Affiliated Hospital of Soochow University, Suzhou, China

2. Department of Radiotherapy and Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China

3. Institution of Radiotherapy and Oncology, Soochow University, Suzhou, China

4. Laboratory for Combined Radiotherapy and Immunotherapy of Cancer, The Second Affiliated Hospital of Soochow University, Suzhou, China

5. Department of Radiology, The Second Affiliated Hospital of Soochow University, Suzhou, China

6. Department of Nuclear Medicine, The Second Affiliated Hospital of Soochow University, Suzhou, China

Abstract

Objective: The prognosis of malignant tumors with peritoneal metastases and cancerous ascites has generally been poor, with limited treatment options. The PRaG regimen, which comprised of hypofractionated radiotherapy, programmed cell death-1 (PD-1) inhibitor, and granulocyte-macrophage colony-stimulating factor (GM-CSF), showed a survival advantage in patients with advanced solid tumors who failed at least the first line of standard systemic treatment. Intraperitoneal infusion of PD-1 inhibitors may be a novel therapeutic strategy for managing malignant ascites. Integrating the PRaG regimen with intraperitoneal perfusion of a PD-1 inhibitor might control malignant ascites and provide further survival benefits in these patients. This proposed study aims to investigate the safety and efficacy of intraperitoneal infusion of serplulimab in combination with the PRaG regimen in patients with simultaneous advanced solid tumors and cancerous ascites who fail at least the first-line treatment. Methods: This proposed study is a prospective, single-arm, open-label, multicenter clinical trial. All eligible patients will receive 2 cycles of intensive treatment, a combination of PRaG regimen with an intraperitoneal infusion of PD-1 inhibitor. The patients who are beneficially treated with intensive treatment will receive consolidation treatment every 2 weeks until ascites disappear, disease progression occurs, intolerable toxicity occurs, or for up to 1 year. Phase I of this study will be conducted using a modified 3 + 3 design. The dose of intraperitoneal infusion of PD-1 inhibitor for phase II will be determined according to dose-limiting toxicity evaluation in the phase I study. Conclusion: This prospective, open-label, multicenter study will potentially lead to intraperitoneal perfusion of a PD-1 inhibitor being a new strategy for malignant ascites patients and provide a meaningful efficacy and safety of the combination of PRaG regimen with an intraperitoneal infusion of PD-1 inhibitor for these patients.

Funder

the Subject construction support project of the Second Affiliated Hospital of Soochow University

National Natural Science Foundation of China

Open Project of Provincial Key Laboratory of Soochow University

Suzhou Radiotherapy Clinical Medical Center

Wu Jieping Medical Foundation

Key Medical Discipline Construction Unit of Jiangsu Province for the 14th Five-year plan

Foundation of Chinese Society of Clinical Oncology

the Project of State Key Laboratory of Radiation Medicine and Protection

the Key R & D plan of Jiangsu Province

Publisher

SAGE Publications

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