黑色素瘤
医学
肿瘤科
癌症
靶向治疗
疾病
临床试验
激酶
转移性黑色素瘤
内科学
癌症研究
生物
细胞生物学
作者
Dirk Schadendorf,Alexander C.J. van Akkooi,Carola Berking,Klaus Griewank,Ralf Gutzmer,Axel Hauschild,Andreas Stang,Alexander Roesch,Selma Ugurel
出处
期刊:The Lancet
[Elsevier BV]
日期:2018-09-01
卷期号:392 (10151): 971-984
被引量:1188
标识
DOI:10.1016/s0140-6736(18)31559-9
摘要
Cutaneous melanoma causes 55 500 deaths annually. The incidence and mortality rates of the disease differ widely across the globe depending on access to early detection and primary care. Once melanoma has spread, this type of cancer rapidly becomes life-threatening. For more than 40 years, few treatment options were available, and clinical trials during that time were all unsuccessful. Over the past 10 years, increased biological understanding and access to innovative therapeutic substances have transformed advanced melanoma into a new oncological model for treating solid cancers. Treatments that target B-Raf proto-oncogene serine/threonine-kinase (BRAF)V600 (Val600) mutations using selected BRAF inhibitors combined with mitogen-activated protein kinase inhibitors have significantly improved response and overall survival. Furthermore, advanced cutaneous melanoma has developed into a prototype for testing checkpoint-modulating agents, which has increased hope for long-term tumour containment and a potential cure. These expectations have been sustained by clinical success with targeted agents and antibodies that block programmed cell-death protein 1 in locoregional disease, which induces prolongation of relapse-free, distant-metastasis-free, and overall survival times.
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