Characterization and Outcomes of Disease Progression in 52 Patients Treated with BRAF-V600 + MEK Inhibitors for Advanced Melanoma.

Dermatology (Basel, Switzerland) Pub Date : 2018-01-01 Epub Date: 2018-08-15 DOI:10.1159/000490891
Philippine Lucas, Serge Boulinguez, Vincent Sibaud, Loïc Mourey, Laurence Lamant, Carle Paul, Nicolas Meyer
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引用次数: 5

Abstract

Background: Combined treatment with BRAF-V600 and MEK inhibitors has significantly improved progression-free and overall survival of patients with BRAF-mutated melanoma. Pattern of disease progression and outcomes in patients have not been fully characterized.

Methods: We conducted a single-center, retrospective, descriptive analysis of a cohort of 52 patients treated with BRAF-V600 + MEK inhibitors for advanced melanoma over a 12-month period. The aim of this study was to characterize disease progression, defined as metastatic pattern, disease kinetics, and response to subsequent therapies, in melanoma patients treated with BRAF-V600 + MEK inhibitors.

Results: Disease progression was observed in 31/52 (59.6%) patients treated with BRAF-V600 + MEK inhibitors. Relapse of melanoma involved the CNS for 22/31 (70.9%) patients with disease progression, including 18/31 (58%) patients who had exclusive intracranial metastases. Sixteen patients died from disease progression. Among the 31 patients who had disease progression, the median time until a relapse was 8 months, and the median survival time after disease progression was 2 months.

Conclusion: Our study shows that, for patients treated with BRAF-V600 + MEK inhibitors who lose response, disease progression was aggressive and had poor outcomes. Most patients had CNS metastases and low rates of therapeutic response to any subsequent therapy.

52例BRAF-V600 + MEK抑制剂治疗晚期黑色素瘤患者的疾病进展特征和结果
背景:BRAF-V600和MEK抑制剂联合治疗可显著改善braf突变黑色素瘤患者的无进展和总生存期。患者的疾病进展模式和结局尚未完全确定。方法:我们对52例接受BRAF-V600 + MEK抑制剂治疗的晚期黑色素瘤患者进行了为期12个月的单中心、回顾性、描述性分析。本研究的目的是表征BRAF-V600 + MEK抑制剂治疗的黑色素瘤患者的疾病进展,定义为转移模式、疾病动力学和对后续治疗的反应。结果:接受BRAF-V600 + MEK抑制剂治疗的患者中有31/52(59.6%)出现疾病进展。22/31(70.9%)的疾病进展患者复发黑色素瘤累及中枢神经系统,其中18/31(58%)的患者只有颅内转移。16例患者死于疾病进展。在31例有疾病进展的患者中,到复发的中位时间为8个月,疾病进展后的中位生存时间为2个月。结论:我们的研究表明,接受BRAF-V600 + MEK抑制剂治疗的患者失去应答,疾病进展具有侵袭性,预后较差。大多数患者有中枢神经系统转移,对任何后续治疗的治疗反应率低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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