Author:
Zurloh M.,Goetz M.,Herold T.,Treckmann J.,Markus P.,Schumacher B.,Albers D.,Rink A.,Rosery V.,Zaun G.,Kostbade K.,Pogorzelski M.,Ting S.,Schmidt H.,Stiens R.,Wiesweg M.,Schuler M.,Kasper Stefan,Virchow I.
Abstract
Abstract
Purpose
Patients with BRAFV600E-mutant metastatic colorectal cancer (mCRC) have a dismal prognosis. The best strategies in these patients remain elusive. Against this background, we report the clinical course of patients with BRAFV600E-mutant mCRC to retrieve the best treatment strategy.
Patients and methods
Clinico-pathological data were extracted from the electronic health records. Kaplan–Meier method was used to estimate overall (OS) and progression-free survival (PFS). Objective response rate (ORR) was assessed according to RECIST 1.1.
Results
In total, 51 patients were enrolled. FOLFOXIRI was administered to 12 patients; 29 patients received FOLFOX or FOLFIRI as first-line treatment. Median OS was 17.6 months. Median PFS with FOLFOXIRI (13.0 months) was significantly prolonged (HR 0.325) as compared to FOLFOX/FOLFIRI (4.3 months). However, this failed to translate into an OS benefit (p = 0.433). Interestingly, addition of a monoclonal antibody to chemotherapy associated with superior OS (HR 0.523). A total of 64.7% patients received further-line therapy, which included a BRAF inhibitor in 17 patients. Targeted therapy associated with very favourable OS (25.1 months).
Conclusion
Patients with BRAFV600E-mutated mCRC benefit from the addition of an antibody to first-line chemotherapy. Further-line treatment including a BRAF inhibitor has a dramatic impact on survival.
Funder
Universitätsklinikum Essen
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology,General Medicine