Yu Irene S, Aubin Francine, Goodwin Rachel, Loree Jonathan M, Mather Cheryl, Sheffield Brandon S, Snow Stephanie, Gill Sharlene
Department of Medical Oncology, BC Cancer Surrey, Surrey, BC, Canada.
Division of Hematology and Oncology, Department of Medicine, Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada.
Ther Adv Med Oncol. 2022 Jul 20;14:17588359221111705. doi: 10.1177/17588359221111705. eCollection 2022.
The systemic therapy management of metastatic colorectal cancer (mCRC) has evolved from primarily cytotoxic chemotherapies to now include targeted agents given alone or in combination with chemotherapy, and immune checkpoint inhibitors. A better understanding of the pathogenesis and molecular drivers of colorectal cancer not only aided the development of novel targeted therapies but led to the discovery of tumor mutations which act as predictive biomarkers for therapeutic response. Mutational status of the gene became the first genomic biomarker to be established as part of standard of care molecular testing, where mutations within exons 2, 3, and 4 predict a lack of response to anti- epidermal growth factor receptor therapies. Since then, several other biomarkers have become relevant to inform mCRC treatment; however, there are no published Canadian guidelines which reflect the current standards for biomarker testing. This guideline was developed by a pan-Canadian advisory group to provide contemporary, evidence-based recommendations on the minimum acceptable standards for biomarker testing in mCRC, and to describe additional biomarkers for consideration.
转移性结直肠癌(mCRC)的系统治疗管理已从主要的细胞毒性化疗发展到如今包括单独使用或与化疗联合使用的靶向药物,以及免疫检查点抑制剂。对结直肠癌发病机制和分子驱动因素的更好理解不仅有助于新型靶向治疗的开发,还导致发现了作为治疗反应预测生物标志物的肿瘤突变。该基因的突变状态成为第一个作为护理标准分子检测一部分而确立的基因组生物标志物,其中外显子2、3和4内的突变预示着对抗表皮生长因子受体治疗无反应。从那时起,其他几种生物标志物也与mCRC治疗相关;然而,尚无反映生物标志物检测当前标准的加拿大已发表指南。本指南由一个泛加拿大咨询小组制定,旨在就mCRC生物标志物检测的最低可接受标准提供当代的、基于证据的建议,并描述其他可供考虑的生物标志物。