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Clinical Trial Summary

In this open-label phase III study, patients with local advanced colon cancer (TanyN+ ,M0, dMMR/MSI-H, at least 10cm from the anus verge)will be scheduled to Group A: receive anti-PD-1 antibody alone (8 cycles, 200mg iv drip Q3W) and Group B (4 or 8 cycles of XELOX: oxaliplatin 130mg/m2 day 1, capecitabine 2000mg/m2 days 1-14, repeated every 21 days). The primary endpoint was 3 Disease-free survival; analyses were done based on all patients with post-randomization data.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05236972
Study type Interventional
Source Sun Yat-sen University
Contact Peirong Ding, professor
Phone +86-13543478645
Email dingpr@sysucc.org.cn
Status Recruiting
Phase Phase 3
Start date January 1, 2022
Completion date December 31, 2028

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