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Clinicopathologic Features and Prognosis of BRAF Mutated Colorectal Cancer Patients.

Authors :
Guan WL
Qiu MZ
He CY
Yang LQ
Jin Y
Wang ZQ
Li YH
Xu RH
Wang FH
Source :
Frontiers in oncology [Front Oncol] 2020 Nov 23; Vol. 10, pp. 563407. Date of Electronic Publication: 2020 Nov 23 (Print Publication: 2020).
Publication Year :
2020

Abstract

Background: BRAF <superscript>V600E</superscript> mutation is associated with poor prognosis of colorectal cancer (CRC) patients, but the comparison of clinic-pathologic features between V600E and non-V600E mutation was not well-known in CRC patients. The aim of this study is to evaluate the clinical and pathological features, prognostic value of BRAF mutations in CRC. Methods: We conducted a retrospective study to characterize the clinical and pathological features and survival of patients with BRAF mutated CRC. Patients were classified according to BRAF status as BRAF <superscript>V600E</superscript> mutation and non-V600E mutations. Difference of characteristics and survival between the two groups was analyzed. Results: There was no significant difference in gender, family history, location of primary tumor, metastatic sites between patients with BRAF -V600E mutation and non-V600E mutations. Patients with V600E mutation were younger than those with non-V600E mutations ( p = 0.002). Patients with BRAF <superscript>V600E</superscript> mutation showed a poorer outcome than those with non-V600E mutations (23.1 vs. 49.9 months, respectively, p = 0.0024). Lack of CDX2 expression was associated with worse prognosis (mOS: 9.4 m vs. not reached, respectively, p = 0.016). Status of V600E mutation did not affect the mPFS and ORR of first-line or second-line treatment. Conclusion: BRAF <superscript>V600E</superscript> mutation defines a distinct subgroup of CRC with worse prognosis. Lack of CDX2 expression is associated with poor OS. Status of V600E mutation did not affect the mPFS of first-line or second-line treatment.<br /> (Copyright © 2020 Guan, Qiu, He, Yang, Jin, Wang, Li, Xu and Wang.)

Details

Language :
English
ISSN :
2234-943X
Volume :
10
Database :
MEDLINE
Journal :
Frontiers in oncology
Publication Type :
Academic Journal
Accession number :
33330032
Full Text :
https://doi.org/10.3389/fonc.2020.563407