Pharmacotherapy for unresectable metastatic colorectal cancer

被引:1
|
作者
Rogers, Jane E. [1 ]
Dasari, Arvind [2 ]
机构
[1] Univ Texas Md Anderson Canc Ctr, Pharm Clin Programs, Houston, TX 77030 USA
[2] Univ Texas Md Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
关键词
Agents; antineoplastic; BRAFV600E mutant; checkpoint inhibitors; colorectal neoplasms; human epidermal growth factor receptor 2; microsatellite instability-high; deficient mismatch repair; FOLFOXIRI PLUS BEVACIZUMAB; EGFR RECHALLENGE THERAPY; OPEN-LABEL; 1ST-LINE TREATMENT; SUBGROUP ANALYSES; SOLID TUMORS; PHASE-II; MULTICENTER; NIVOLUMAB; BIOMARKER;
D O I
10.1080/14656566.2021.1982895
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction Unresectable metastatic colorectal cancer (mCRC) has a poor prognosis. Emerging treatment paradigms have improved outcomes in selected unresectable mCRC cases. Recent therapeutic advancements are due in part to a shift in trial designs. By examining CRC as a heterogeneous group of various tumor subtypes, researchers have identified molecular distinctions that have led to promising targets. Areas covered Nineteen antineoplastic agents are included in the National Comprehensive Cancer Network guidelines for the palliative management of mCRC. However, not all patients will be candidates for each agent. New therapies for rare mCRC subtypes have emerged. Herein, the authors review these rare mCRC subtypes: microsatellite instability-high/deficient mismatch repair, BRAFV600E-mutant, and human epidermal growth factor receptor 2-positive tumors. Additionally, they provide an overview of unresectable mCRC management and future directions. Expert opinion Treatment in the majority of mCRC patients (RAS wild-type or RAS-mutant, microsatellite instability-stable or -low/mismatch repair-proficient, BRAFV600E wild-type, or HER2-negative) needs further advancement and remains an unmet need. The authors believe that the key to identifying more breakthroughs in these mCRC patients is to continue to differentiate their tumors molecularly and clinically.
引用
收藏
页码:211 / 220
页数:10
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