European expert panel consensus on the clinical management of BRAFV600E-mutant metastatic colorectal cancer

被引:7
|
作者
Martinelli, Erika [1 ]
Arnold, Dirk [2 ]
Cervantes, Andres [3 ,4 ]
Stintzing, Sebastian [5 ]
Van Cutsem, Eric [6 ,7 ]
Tabernero, Josep [8 ,9 ]
Taieb, Julien [10 ]
Wasan, Harpreet [11 ]
Ciardiello, Fortunato [12 ]
机构
[1] Univ Campania Luigi Vanvitelli, Dept Precis Med, Div Med Oncol, I-80131 Naples, Italy
[2] Asklepios Tumorzentrum Hamburg, AK Altona, Dept Oncol & Hematol, Hamburg, Germany
[3] Univ Valencia, INCL Biomed Res Inst, Dept Med Oncol, Valencia, Spain
[4] CIBERONC, Inst Salud Carlos III, Madrid, Spain
[5] Charite Univ Med Berlin, Dept Hematol Oncol & Canc Immunol CCM, D-10117 Berlin, Germany
[6] Univ Hosp Gasthuisberg Leuven, Dept Digest Oncol, Leuven, Belgium
[7] KULeuven, Leuven, Belgium
[8] IOB Quiron, Vall Hebron Hosp Campus, Dept Med Oncol, Barcelona 08035, Spain
[9] IOB Quiron, Vall Hebron Inst Oncol VHIO, Barcelona 08035, Spain
[10] Univ Paris Cite, Georges Pompidou European Hosp, Assitance Publ Hop Paris AP HP Paris Ctr, Dept Gastroenterol & GI Oncol, Paris, France
[11] Hammersmith Hosp, Imperial Coll Healthcare NHS Trust, Dept Canc Med, London W12 0HS, England
[12] Univ Campania Luigi Vanvitelli, Dept Precis Med, Div Med Oncol, I-80131 Naples, Italy
关键词
Metastatic colorectal cancer; BRAF; Consensus; Treatment; MISMATCH REPAIR-DEFICIENT; PLUS CETUXIMAB; COMBINED BRAF; 1ST-LINE TREATMENT; SUBGROUP ANALYSES; OPEN-LABEL; MEK; ENCORAFENIB; INHIBITION; DABRAFENIB;
D O I
10.1016/j.ctrv.2023.102541
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastatic colorectal cancer (mCRC) is a heterogenous disease caused by various genetic alterations. The BRAFV600E mutation occurs in approximately 8-12% of patients and is characterised by an aggressive clinical course and poor prognosis. Here we review the current knowledge on BRAFV600E-mutant mCRC and provide a series of consensus statements on its clinical management. The treatment landscape for BRAFV600E-mutant mCRC has changed greatly due to the emergence of molecular targeted therapies (including BRAF inhibitors) and immune checkpoint inhibitors. A scientific literature search identified available data on molecular testing, treatments, and clinical monitoring of patients with BRAFV600E-mutant mCRC. Consensus statements were dis-cussed and developed by a European expert panel. This manuscript provides consensus management guidance for different clinical presentations of BRAFV600E-mutant mCRC and makes recommendations regarding treatment sequencing choices. To guide appropriate clinical management and treatment decisions for mCRC patients, tumour tissue analysis for DNA mismatch repair/microsatellite status and, at a minimum, KRAS, NRAS, and BRAF mutational status is mandatory at the time of diagnosis. Finally, we discuss the rapidly evolving treatment landscape for BRAFV600E-mutant mCRC and define priorities for the development of novel therapeutic strategies that are needed to improve patient outcomes.
引用
收藏
页数:11
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