RecruitingPhase 2Phase 3NCT06958419

Node-Sparing Short-Course Radiotherapy Plus Chemotherapy, Bevacizumab and PD-1 Inhibitor in Metastatic pMMR/MSS Colorectal Cancer (MODIFI-CRC)

Node-Sparing Short-Course Radiotherapy Followed by First-Line Chemotherapy Plus Bevacizumab and PD-1 Inhibitor Versus Chemotherapy Plus Bevacizumab Alone in Metastatic pMMR/MSS Colorectal Cancer: A Randomized, Phase II/III Trial (MODIFI-CRC)


Sponsor

Sixth Affiliated Hospital, Sun Yat-sen University

Enrollment

286 participants

Start Date

May 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The current standard first-line treatment for metastatic colorectal cancer is chemotherapy combined with targeted therapy, yet the prognosis remains poor. Although combining immunotherapy, anti-angiogenic agents, and chemotherapy has shown some efficacy in MSS/pMMR metastatic patients, progression-free survival (PFS) remains suboptimal. Radiotherapy-particularly high-dose radiotherapy-can enhance tumor antigen release and potentially improve the response of MSS/pMMR colorectal cancer to PD-1 inhibitors. Tumor-draining lymph nodes (TDLNs) are key sites for PD-1-mediated anti-tumor activity, but radiation-induced damage and fibrosis may impair their immune function. Prior studies have reported a remarkable pathologic complete response (pCR) rate of 77.8% using node-sparing radiotherapy in locally advanced rectal cancer. This phase II/III study aims to evaluate whether node-sparing modified short-course radiotherapy combined with chemotherapy, bevacizumab, and PD-1 blockade can improve objective response rate (ORR) in phase II and progression-free survival (PFS) in phase III, together with treatment tolerance, and overall prognosis in patients with pMMR/MSS metastatic colorectal cancer.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination treatment for metastatic colorectal cancer that doesn't respond well to immunotherapy (called pMMR/MSS colorectal cancer). The approach combines short-course radiation therapy with chemotherapy, a targeted drug (bevacizumab), and an immunotherapy (PD-1 inhibitor), using a special radiation technique designed to preserve nearby lymph nodes. **You may be eligible if...** - You are between 18 and 75 years old - You have been diagnosed with metastatic colorectal adenocarcinoma (pMMR/MSS type) - Your cancer cannot be surgically removed - You have not had prior chemotherapy for metastatic or recurrent disease - You have at least one measurable tumor on imaging - Your overall health is good (ECOG 0–1) and organ function is adequate **You may NOT be eligible if...** - Your cancer is MSI-H or dMMR (which responds better to immunotherapy alone) - Your cancer has spread to the brain - You have active autoimmune conditions that could worsen with immunotherapy - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

COMBINATION_PRODUCTNode-Sparing Radiotherapy plus first-line therapy

Patients will receive node-sparing modified short-course radiotherapy, followed by 8 cycles of FOLFOX chemotherapy combined with bevacizumab and a PD-1 inhibitor. After induction therapy, patients will continue with maintenance therapy using bevacizumab, PD-1 inhibitor, and 5-fluorouracil (5-FU), administered every 2 weeks (Q2W).

COMBINATION_PRODUCTFirst-line treatment

Patients will receive 8 cycles of FOLFOX chemotherapy combined with bevacizumab, followed by maintenance therapy with bevacizumab and 5-fluorouracil (5-FU), administered every 2 weeks (Q2W).


Locations(1)

The Sixth Affiliated Hospital of Sun Yat-sen University

Guangzhou, Guangdong, China

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NCT06958419


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