Department of Oncology and Hematology, Division of Oncology, University of Modena and Reggio Emilia, 41121 Modena, Italy.
IRCCS San Raffaele Scientific Institute Hospital, 20019 Milan, Italy.
Int J Mol Sci. 2019 Oct 28;20(21):5369. doi: 10.3390/ijms20215369.
Colorectal cancer (CRC) is one of the leading causes of mortality and morbidity in the world. It is a heterogeneous disease, which can be classified into different subtypes, characterized by specific molecular and morphological alterations. In this context, BRAF mutations are found in about 10% of CRC patients and define a particular subtype, characterized by a dismal prognosis, with a median survival of less than 12 months. Chemotherapy plus bevacizumab is the current standard therapy in first-line treatment of BRAF-mutated metastatic CRC (mCRC), with triplet (FOLFOXIRI) plus bevacizumab as a valid option in patients with a good performance status. BRAF inhibitors are not so effective as compared to melanoma, because of various resistance mechanisms. However, the recently published results of the BEACON trial will establish a new standard of care in this setting. This review provides insights into the molecular underpinnings underlying the resistance to standard treatment of BRAF-mutated CRCs, with a focus on their molecular heterogeneity and on the research perspectives both from a translational and a clinical point of view.
结直肠癌(CRC)是全球导致死亡和发病的主要原因之一。它是一种异质性疾病,可以分为不同的亚型,其特征是特定的分子和形态改变。在这种情况下,BRAF 突变约见于 10%的 CRC 患者,并定义了一个特殊的亚型,其预后不良,中位生存期不到 12 个月。化疗加贝伐珠单抗是 BRAF 突变转移性结直肠癌(mCRC)一线治疗的标准疗法,对于体能状态良好的患者,三联(FOLFOXIRI)加贝伐珠单抗是一种有效的选择。与黑色素瘤相比,BRAF 抑制剂的效果并不那么显著,因为存在多种耐药机制。然而,最近发表的 BEACON 试验结果将在这一领域确立新的治疗标准。本文综述了 BRAF 突变型 CRC 对标准治疗产生耐药性的分子基础,重点介绍了其分子异质性,以及从转化和临床角度的研究前景。