Shuford Rebecca A, Cairns Ashley L, Moaven Omeed
Department of Surgery, Wake Forest University, Winston-Salem, NC 27157, USA.
Section of Surgical Oncology, Department of Surgery, Mayo Clinic Florida, Jacksonville, FL 32224, USA.
Cancers (Basel). 2020 Nov 23;12(11):3481. doi: 10.3390/cancers12113481.
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 (), epithelial growth factor receptor (EGFR), vascular endothelial growth factor VEGF, microsatellite instability, mismatch repair, and () with established clinical implications. 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.
转移性结直肠癌的遗传和分子基础已被研究了数十年,这些研究结果在临床决策中的适用性也在不断发展。分子研究转化方面的进展为转移性结直肠癌(mCRC)治疗中化疗方案的定制提供了依据,这些依据为多项实践指南提供了参考。多种遗传和分子途径已被确定在转移性结直肠癌的发病机制中具有临床意义。这些途径包括()、表皮生长因子受体(EGFR)、血管内皮生长因子VEGF、微卫星不稳定性、错配修复,以及(),它们都具有既定的临床意义。错配修复途径中的突变和缺陷分别指导基于抗EGFR疗法和免疫疗法的给药决策。此外,还有几种新兴途径和治疗方式尚未在mCRC治疗中得到主流应用,有待进一步研究。靶向治疗领域的成熟数据为mCRC治疗中各种治疗方案的使用或避免提供了循证支持,而新兴途径和平台则为将精准方法转变为个性化治疗的未来发展提供了展望。