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Clinical Trial Summary

This study was an observational cohort study to investigate the efficacy predictors of fuquinitinib combined with anti-PD-1 monoclonal antibody for third-line treatment and above in Chinese patients with advanced colorectal cancer.


Clinical Trial Description

Patients with histologically confirmed metastatic or unresectable MSS/MSI-L/pMMR colorectal adenocarcinoma refractory to or intolerant of fluorouracil, oxaliplatin and irinotecan based systemic treatment, were enrolled in the study. All patients will receive a third line therapy with fruquintinib and anti-PD-1 antibody. Clinical and radiographic assessment will be performed regularly. Patients will be treated until disease progression, untolerable toxicity or withdrawal of consent. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05635149
Study type Observational [Patient Registry]
Source Wuhan Union Hospital, China
Contact Hongli Liu, PhD
Phone +86-027-85871962
Email hongli_liu@hust.edu.cn
Status Recruiting
Phase
Start date January 1, 2022
Completion date September 30, 2023

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