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Cutaneous toxicities of BRAF inhibitors: Clinical and pathological challenges and call to action

机译:BRAF抑制剂的皮肤毒性:临床和病理挑战及行动呼吁

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摘要

Somatic mutations in the BRAF gene have been identified as the most frequent and relevant to develop targeted molecular therapies in melanoma. Recently, seminal clinical trials have provided indisputable evidence that BRAF inhibitors improve response rate, progression free and overall survival in BRAFV600 mutated metastatic melanoma patients, thus representing the novel standard of care. Dermatological "off target" effects of these so-called 'targeted therapies' have to be considered, however, and among them the most intriguing are cutaneous adverse reactions. Skin toxicity is of relevance for at least three reasons: (1) it worsens the patient's quality of life and may be difficult to manage, (2) its heterogeneous clinical presentation differs from the clinico-pathological pictures observed in patients who do not receive BRAF inhibitors, and; (3) onset of skin cancer represents a model of carcinogenesis which may help to better understand the potential visceral tumorigenesis induced by BRAF inhibitors. This manuscript summarizes and critically reviews the state of the art of skin toxicity associated with BRAF inhibitors. Special attention will be paid to clinical presentation and histopathological findings, as well as related challenges for clinicians, pathologists, and basic scientists.
机译:已经确定BRAF基因中的体细胞突变是最常见的,并且与开发黑色素瘤的靶向分子疗法有关。最近,开创性的临床试验提供了无可争议的证据,证明BRAF抑制剂可改善BRAFV600突变的转移性黑色素瘤患者的应答率,无进展和总体生存率,从而代表了新的治疗标准。然而,必须考虑这些所谓“靶向疗法”的皮肤病学“脱靶”效应,其中最引人入胜的是皮肤不良反应。皮肤毒性的相关性至少出于以下三个原因:(1)它会恶化患者的生活质量,并且可能难以控制;(2)其异质性临床表现与未接受BRAF的患者所观察到的临床病理学图像有所不同抑制剂,以及(3)皮肤癌的发作代表了一种癌发生模型,可能有助于更好地了解BRAF抑制剂诱导的潜在内脏肿瘤发生。该手稿总结并严格审查了与BRAF抑制剂有关的皮肤毒性的技术现状。将特别注意临床表现和组织病理学发现,以及对临床医生,病理学家和基础科学家的相关挑战。

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