Establishment and validation of the deep learning signature of bevacizumab efficacy in initially unresectable CRLM patients
Initially unresectable CRLM patients were included in this study. The tumor response was assessed by local MDT group. The signature will classified patients into responder or non-responder group. We will administer mFOLFOX6+bevacizumab regimen to responders, and FOLFOXIRI regimen to non-responders.
Study Type
OBSERVATIONAL
Enrollment
302
AEM A:The specialist's decision to add bevacizumab to chemotherapy will be based on their own judgment ARM B:The patient's PET/CT imaging, pathology, and clinical information were input into the signature, and the FOLFOX+Bevacizumab regimen was selected when the output label was 1. FOLFOXIRI chemotherapy regimen was selected when the output label was 0
Zhongshan hospital
Shanghai, Shanghai Municipality, China
response rate
response rate will be assessed by local MDT every two months
Time frame: 6 months
progression free survival
progression free survival will be assessed by local MDT every two months during
Time frame: 3 years
overall survival
overall survival will be assessed by researchers every two months during treatment, and telephone follow-up every three month after treatment
Time frame: 5 years
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