Precision medicine for metastatic colorectal cancer: an evolving era

被引:45
|
作者
Guler, Irem [1 ]
Askan, Gokce [2 ]
Klostergaard, Jim [3 ]
Sahin, Ibrahim Halil [4 ]
机构
[1] Baskent Univ, Sch Med, Dept Med, Ankara, Turkey
[2] Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10021 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77030 USA
[4] Emory Univ, Sch Med, Winship Canc Inst, 1365 Clifton Rd NE 2080, Atlanta, GA 30322 USA
关键词
Colorectal Cancer; anti-EGFR; mismatch repair genes; MSI-H; MMR-D; BRAF; HER2; BRCA; PALB2; POLE; POLD1; NTRK; ALK; ROS1; FGFR; immunotherapy; immune checkpoint inhibitors; precision medicine; OXALIPLATIN-BASED CHEMOTHERAPY; MISMATCH REPAIR DEFICIENCY; CETUXIMAB PLUS IRINOTECAN; CIRCULATING TUMOR-CELLS; FACTOR RECEPTOR PATHWAY; PHASE-III TRIAL; WILD-TYPE KRAS; 1ST-LINE TREATMENT; COLON-CANCER; OPEN-LABEL;
D O I
10.1080/17474124.2019.1663174
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction: Metastatic colorectal cancer (CRC) remains a dilemma for cancer researchers with an increasing incidence in the younger patient population. Until the last decade, limited therapeutic options were available for metastatic CRC patients leading to relatively poor clinical outcomes. Areas covered: With advances in genome sequencing technology and reductions in the cost of next-generation sequencing, molecular profiling has become more accessible for cancer researchers and clinical investigators, which has furthered our understanding of the molecular behavior of CRC. This progress has recently translated into significant advances in molecular-based therapeutics and led to the development of new target-specific agents in metastatic CRC patients. In this review article, we extensively elaborate on genomic alterations seen in CRC patients including, but not limited to, EGFR, MMR, BRAF, HER2, NTRKs, FGFR, BRCA1/2, PALB2, POLE, and POLD1 genes, all of which are potentially actionable by either an FDA-approved agent or in a clinical trial setting. Expert opinion: We strongly recommend molecular profiling in metastatic CRC patients during the early course of their disease, as this may provide therapeutic and prognostic information that can guide clinicians to practice precision medicine. Patients with potentially actionable genes should be considered for targeting agents based on molecular alterations.
引用
收藏
页码:919 / 931
页数:13
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