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A validated prognostic classifier for V600E BRAF-mutated metastatic colorectal cancer: the 'BRAF BeCool' study.
- Source :
-
European journal of cancer (Oxford, England : 1990) [Eur J Cancer] 2019 Sep; Vol. 118, pp. 121-130. Date of Electronic Publication: 2019 Jul 19. - Publication Year :
- 2019
-
Abstract
- Background: Despite the well-known negative prognostic value of the <superscript>V600E</superscript> BRAF mutation in patients with metastatic colorectal cancer (mCRC), its outcome is quite heterogeneous, and the basis for this prognostic heterogeneity should be better defined.<br />Methods: Two large retrospective series of <superscript>V600E</superscript> BRAF-mutated mCRC from 22 institutions served as an exploratory and validation set to develop a prognostic score. The model was internally and externally validated.<br />Results: A total of 395 <superscript>V600E</superscript> BRAF-mutated mCRCs were included in the exploratory set. Performance status, CA19.9, lactate dehydrogenase, neutrophil/lymphocyte ratio, grading and liver, lung and nodal involvement emerged as independent prognostic factors for overall survival (OS). Two different scoring systems were built: a 'complete' score (0-16) including all significant covariates and a 'simplified' score (0-9), based only on clinicopathological covariates, and excluding laboratory values. Adopting the complete score, proportions of patients with a low (0-4), intermediate (5-8) and high (9-16) score were 44.7%, 42.6% and 12.6%, respectively. The median OS was 29.6, 15.5 (hazard ratio [HR] for intermediate vs low risk: 2.16, 95% confidence interval [CI]: 1.44-3.22, p < .001) and 6.6 months (HR for high vs low risk: 4.72, 95% CI: 2.72-8.20, p < .001). Similar results were observed also after adjusting for the type of first-line treatment and adopting the simplified score. The simplified prognostic score derived from the exploratory set was then applied to the validation set for external confirmation.<br />Conclusions: These scoring systems are based on easy-to-collect data and defined specific subgroups with relevant differences in their life expectancy. These tools could be useful in clinical practice, would allow better stratification of patients in clinical trials and may be adopted for proper adjustments in exploratory translational analyses.<br /> (Copyright © 2019 Elsevier Ltd. All rights reserved.)
- Subjects :
- Adult
Aged
Aged, 80 and over
Colorectal Neoplasms mortality
Colorectal Neoplasms pathology
Colorectal Neoplasms therapy
Female
Genetic Predisposition to Disease
Humans
Italy
Male
Middle Aged
Neoplasm Metastasis
Phenotype
Predictive Value of Tests
Prognosis
Retrospective Studies
Risk Assessment
Risk Factors
Young Adult
Biomarkers, Tumor genetics
Colorectal Neoplasms genetics
DNA Mutational Analysis
Mutation
Proto-Oncogene Proteins B-raf genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0852
- Volume :
- 118
- Database :
- MEDLINE
- Journal :
- European journal of cancer (Oxford, England : 1990)
- Publication Type :
- Academic Journal
- Accession number :
- 31330487
- Full Text :
- https://doi.org/10.1016/j.ejca.2019.06.008