patients with chemotherapy-naive RAS, wild-type, unresectable metastatic colorectal cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients who were enrolled in the PARADIGM trial at 197 domestic institutions between March 2015 and July 2017 and underwent conversion surgery after receiving mFOLFOX6 plus bevacizumab or mFOLFOX6 plus panitumumab (excluding cases that were not included in the efficacy analysis of the PARADIGM trial).
Exclusion criteria
Exclusion criteria: 1. Patients deemed inappropriate for participation in this study by the principal investigator or researchers. 2. Patients who have expressed their wish not to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overall survival (OS),progression-free survival (PFS),and recurrence-free survival (RFS) in the conversion surgery cohort OS,PFS,and RFS in the conversion surgery cohort,stratified by liver-limited vs.non-liver-limited metastases OS,PFS,and RFS in the conversion surgery cohort,stratified by tumor-associated gene mutations OS and PFS in the entire study population OS and PFS in the entire study population,stratified by liver-limited vs.non-liver-limited metastases OS and PFS in the entire study population,stratified by tumor-associated gene mutations | — |
Countries
Japan
Contacts
Graduate School of Medical Sciences, Kyushu University Department of Surgery and Science