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BRAF 突变型结直肠癌:临床与分子研究进展

BRAF-Mutated Colorectal Cancer: Clinical and Molecular Insights.

机构信息

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.

出版信息

Int J Mol Sci. 2019 Oct 28;20(21):5369. doi: 10.3390/ijms20215369.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cf3/6861966/b507291f0250/ijms-20-05369-g001.jpg

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