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[晚期黑色素瘤中BRAF抑制剂和MEK抑制剂毒性的管理]

[Management of toxicities of BRAF inhibitors and MEK inhibitors in advanced melanoma].

作者信息

Sibaud Vincent, Baric Lilian, Cantagrel Alain, Di Palma Mario, Ederhy Stéphane, Paques Michel, Perlemuter Gabriel

机构信息

Institut universitaire du cancer Toulouse - Oncopole, départements d'oncologie médicale et oncodermatologie, Toulouse, France.

Institut universitaire du cancer Toulouse - Oncopole, départements d'oncologie médicale et oncodermatologie, Toulouse, France.

出版信息

Bull Cancer. 2021 May;108(5):528-543. doi: 10.1016/j.bulcan.2020.12.014. Epub 2021 Mar 31.

Abstract

Major therapeutic advances have been made recently in the treatment of metastatic melanoma, due to the development of targeted therapies, namely BRAF and MEK inhibitors, in patients with BRAF V600 mutation. Combinations of vemurafenib+cobimetinib, dabrafenib+trametinib, et encorafenib+binimetinib, evaluated in coBRIM, COMBI-d/COMBI-v and COLUMBUS trials respectively have been approved in this indication. Toxicities induced by combination therapies are different from those reported with monotherapies, in terms of frequency and intensity. Physicians who treat melanoma patients thus face news issues relating to prevention, detection and treatment of these adverse events. This paper summarizes tolerance data from the three pivotal trials (coBRIM, COMBI-v and COLUMBUS) and issues recommendations for the specific management of main toxicities, based on experts' opinion. We discuss dermatological, ophthalmological, cardiovascular, digestive, musculoskeletal, renal and general toxicities and propose a timetable for examinations to be performed before and during treatment.

摘要

由于针对BRAF V600突变患者开发了靶向疗法,即BRAF和MEK抑制剂,转移性黑色素瘤的治疗最近取得了重大进展。分别在coBRIM、COMBI-d/COMBI-v和COLUMBUS试验中评估的维莫非尼+考比替尼、达拉非尼+曲美替尼以及恩考芬尼+比美替尼的联合用药已获该适应症批准。联合疗法引起的毒性在频率和强度方面与单药治疗报告的毒性不同。因此,治疗黑色素瘤患者的医生面临着与这些不良事件的预防、检测和治疗相关的新问题。本文总结了三项关键试验(coBRIM、COMBI-v和COLUMBUS)的耐受性数据,并根据专家意见对主要毒性的具体管理提出建议。我们讨论了皮肤、眼科、心血管、消化、肌肉骨骼、肾脏和全身毒性,并提出了治疗前和治疗期间进行检查的时间表。

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