Targeted chemotherapy of metastatic melanoma: the impact of tumor cell heterogeneity

Diane Kovacic, J. Carlson, A. Slominski
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引用次数: 1

Abstract

Evaluation of: Flaherty KT, Infante JR, Daud A et al. Combined BRAF and MEK inhibition in melanoma with BRAF V600 mutations. N. Engl. J. Med. 367(18), 1694–1703 (2012).The treatment of metastatic melanoma with BRAF inhibitors initially gave dramatic results compared with standard chemotherapy with significant progression-free survival times. Unfortunately, within a matter of months, the melanomas become refractory to anti-BRAF-targeted therapy and some patients experience toxicity in the form of primary cutaneous squamous cell carcinomas. While recent reports of dual therapy targeting the MAPK pathway (e.g., dabrafenib and trametinib) show increased response rates and less toxicity, it is not apparent that overall survival has been significantly impacted. While targeted therapy has significantly altered the management of melanoma, novel approaches and strategies will likely have to be employed to counter melanoma cell heterogeneity and the selection of resistant clones.
转移性黑色素瘤的靶向化疗:肿瘤细胞异质性的影响
评价:Flaherty KT, Infante JR, Daud A等。BRAF和MEK联合抑制BRAF V600突变黑色素瘤。心血管病。中华医学杂志,367(18),1694-1703(2012)。与标准化疗相比,BRAF抑制剂治疗转移性黑色素瘤最初取得了显著的效果,无进展生存期显著。不幸的是,在几个月内,黑色素瘤对抗braf靶向治疗变得难治性,一些患者以原发性皮肤鳞状细胞癌的形式出现毒性。虽然最近报道的针对MAPK通路的双重治疗(例如,达非尼和曲美替尼)显示出更高的反应率和更低的毒性,但总体生存率并未明显受到显著影响。虽然靶向治疗已经显著改变了黑色素瘤的治疗,但可能必须采用新的方法和策略来对抗黑色素瘤细胞的异质性和耐药克隆的选择。
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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