Real-world treatment patterns and outcomes based on RAS/BRAF status in metastatic colorectal cancer-Analysis of the Prospective Dutch Colorectal Cancer cohort

被引:0
作者
van Nassau, Sietske C. M. W. [1 ]
Zwart, Koen [1 ]
van Der Baan, Frederieke H. [1 ]
Vink, Geraldine R. [1 ,2 ]
Elferink, Marloes A. G. [2 ]
Snaebjornsson, Petur [3 ,4 ]
May, Anne M. [5 ]
Koopman, Miriam [1 ]
Roodhart, Jeanine M. L. [1 ]
机构
[1] Univ Utrecht, Univ Med Ctr Utrecht, Dept Med Oncol, Utrecht, Netherlands
[2] Netherlands Comprehens Canc Org IKNL, Dept Res & Dev, Utrecht, Netherlands
[3] Netherlands Canc Inst, Dept Pathol, Amsterdam, Netherlands
[4] Univ Iceland, Fac Med, Reykjavik, Iceland
[5] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Dept Epidemiol & Hlth Econ, Utrecht, Netherlands
关键词
BRAF; metastatic colorectal cancer; RAS; real-world; treatment patterns; FOLFOXIRI PLUS BEVACIZUMAB; CLINICAL-TRIAL; OPEN-LABEL; FOLFIRI; SURVIVAL; THERAPY; PHASE-3; LINES;
D O I
10.1002/ijc.35410
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The treatment landscape for metastatic colorectal cancer (mCRC) has evolved into a continuum of care with an essential role for biomarkers and molecular subgroups. Treatment guidelines are primarily based on trial results; however, populations and outcomes differ from clinical practice. To support the interpretation of trial results and to assist in tailored patient counseling, we evaluated real-world treatment patterns and outcomes according to RAS/BRAF status. We included all patients diagnosed with BRAF(V600E)-mutated mCRC in 2015-2020, participating in the Prospective Dutch Colorectal Cancer cohort study, plus a 1:2 random selection of patients with RAS-mutated and double wild-type mCRC. We evaluated differences in administered lines of treatment (LOTs), local treatment, attrition rates, treatment duration, progression-free survival (PFS) and overall survival (OS). 178 BRAF(V600E)-mutated, 221 RAS-mutated, and 174 double wild-type patients were included. Of BRAF(V600E)-mutated patients, 26% received >= 3 LOTs, compared to 42% and 47% of the RAS-mutated and double wild-type patients, respectively (p = .002). Local treatment was performed in 25% of BRAF(V600E)-mutated, 43% of RAS-mutated, and 49% of double wild-type patients (p < .001). Median OS from diagnosis was 15.4, 24.1, and 32.6 months, respectively (p < .001) and loss of prognostic value of RAS/BRAF was observed from the 3rd LOT onwards (p = .17 and p = .54). This paper provides a comprehensive overview of the treatment landscape of mCRC per RAS/BRAF status in daily clinical practice. The observed substantial treatment heterogeneity within and between molecular subgroups underlines the importance of collecting real-world data to address post-trial knowledge gaps and to optimize individualized counseling for all mCRC patients.
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页数:13
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