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Clinical Trial Summary

The objective is to investigate the efficacy and safety of Envafolimab combined with XELOX in neoadjuvant therapy for locally advanced colon cancer


Clinical Trial Description

According to the 2019 NCCN guidelines, immunocheckpoint inhibitors are recommended for first-line treatment of metastatic colon cancer patients with high microsatellite instability (msi-h) or mismatched gene deletion (dMMR) who are not suitable for intensive treatment, and for all patients with second-line or above msi-h /dMMR treatment. This study is a single-center, single-arm phase II study, patients received neoadjuvant therapy with Envafolimab combined with XELOX regimen, with one treatment cycle every 3 weeks and after two cycles accept surgery. To determine the pathologic downstage rates at time of radical resection of colon cancer following neoadjuvant treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05335460
Study type Interventional
Source Fujian Cancer Hospital
Contact Zaisheng Ye
Phone 13950203076
Email flyingengel@sina.com
Status Not yet recruiting
Phase Phase 2
Start date May 2022
Completion date May 2024

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