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Allied therapies against BRAF-mutated advanced colon cancer: the right plans to win the battle

机译:针对BRAF突变的晚期结肠癌的联合疗法:赢得战斗的正确计划

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In the era of molecular therapies, various targets in different pathways were identified and specific agents were developed with acceptable efficacy rates. BRAF, one of these targets from the family of MAPK, is mutated in different malignancies: melanomas, thyroid cancers, hairy cell leukemia, lung cancer and colorectal cancer [1]. Targeting this mutation with anti-BRAF agents showed interesting response rates in BRAF-mutated melanomas, thyroid cancers and hairy cell leukemia; however their outcomes were disappointing in this subgroup of colorectal cancers [2]. Thus, vemurafenib (anti-BRAF) was first approved as single-agent therapy in BRAF-mutated unresectable and meta-static melanoma; then, the combination of vemurafenib and trametinib (anti-MEK) showed better results than single agent in the same indication and was approved by the US FDA as a standard of care [3,4].
机译:在分子疗法时代,已确定了不同途径的各种靶标,并开发了具有可接受疗效率的特异性药物。 BRAF是MAPK家族的靶标之一,在不同的恶性肿瘤中发生突变:黑色素瘤,甲状腺癌,毛细胞白血病,肺癌和大肠癌[1]。用抗BRAF剂靶向这种突变在BRAF突变的黑色素瘤,甲状腺癌和毛细胞白血病中显示出令人感兴趣的反应率。然而,在这一组大肠癌中,其结果令人失望[2]。因此,维拉非尼(抗BRAF)首先被批准用于BRAF突变的不可切除和转移性黑色素瘤的单药治疗。然后,在相同适应症中,维拉非尼和曲美替尼(抗MEK)的组合显示出比单药更好的结果,并被美国FDA批准为护理标准[3,4]。

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