Precision Approaches in the Management of Colorectal Cancer: Current Evidence and Latest Advancements towards Individualizing the Treatment

被引:11
作者
Shuford, Rebecca A. [1 ]
Cairns, Ashley L. [1 ]
Moaven, Omeed [2 ]
机构
[1] Wake Forest Univ, Dept Surg, Winston Salem, NC 27157 USA
[2] Mayo Clin Florida, Dept Surg, Sect Surg Oncol, Jacksonville, FL 32224 USA
关键词
molecular targeted therapies; colorectal cancer; precision oncology; therapy resistance; GROWTH-FACTOR RECEPTOR; EGFR MONOCLONAL-ANTIBODIES; DEFECTIVE MISMATCH REPAIR; CETUXIMAB PLUS IRINOTECAN; COLON-CANCER; PHASE-III; MICROSATELLITE INSTABILITY; 1ST-LINE TREATMENT; T-CELLS; AMERICAN SOCIETY;
D O I
10.3390/cancers12113481
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Metastatic colorectal cancer (mCRC) represents a significant burden in cancer-related morbidity and mortality. The study of mCRC-related genetic alterations and the molecular landscape of the disease has been ongoing and continues to improve the efficacy of the available treatment options. Here, we review various molecular pathways that are involved in colorectal carcinogenesis with driving mutations that could be targeted for precision approaches in the treatment of mCRC. We summarize groundbreaking clinical trials that are shaping the evolving role of precision approaches in the practice guidelines and discuss the latest advancements in emerging new modalities, novel technologies, and future directions toward individualizing the managemet approaches to the treatment of colorectal cancer. The genetic and molecular underpinnings of metastatic colorectal cancer have been studied for decades, and the applicability of these findings in clinical decision making continues to evolve. Advancements in translating molecular studies have provided a basis for tailoring chemotherapeutic regimens in metastatic colorectal cancer (mCRC) treatment, which have informed multiple practice guidelines. Various genetic and molecular pathways have been identified as clinically significant in the pathogenesis of metastatic colorectal cancer. These include rat sarcoma (RAS), epithelial growth factor receptor (EGFR), vascular endothelial growth factor VEGF, microsatellite instability, mismatch repair, and v-raf murine sarcoma viral oncogene homolog b1 (BRAF) with established clinical implications. RAS mutations and deficiencies in the mismatch repair pathway guide decisions regarding the administration of anti-EGFR-based therapies and immunotherapy, respectively. Furthermore, there are several emerging pathways and therapeutic modalities that have not entered mainstream use in mCRC treatment and are ripe for further investigation. The well-established data in the arena of targeted therapies provide evidence-based support for the use or avoidance of various therapeutic regimens in mCRC treatment, while the emerging pathways and platforms offer a glimpse into the future of transforming a precision approach into a personalized treatment.
引用
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页码:1 / 23
页数:24
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