Immunotherapy for advanced melanoma: Fulfilling the promise

被引:37
|
作者
Gogas, Helen [1 ]
Polyzos, Aristidis [1 ]
Kirkwood, John [2 ]
机构
[1] Univ Athens, Sch Med, Dept Med 1, Laikon Gen Hosp, Athens 11510, Greece
[2] Univ Pittsburgh, Inst Canc, Hillman Canc Ctr, Pittsburgh, PA USA
关键词
Metastatic melanoma; Immunotherapy; CTLA-4; Blocking antibodies; Tremelimumab; Ipilimumab; Anti-PD1; RANDOMIZED PHASE-III; ANTIGEN; 4; CTLA-4; METASTATIC MELANOMA; SUBCUTANEOUS INTERLEUKIN-2; COMBINATION IMMUNOTHERAPY; MALIGNANT-MELANOMA; ANTITUMOR-ACTIVITY; TUMOR-REGRESSION; PLUS DACARBAZINE; PROSTATE-CANCER;
D O I
10.1016/j.ctrv.2013.04.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The incidence of melanoma is increasing worldwide and despite early detection and intervention, the number of patients dying from metastatic disease continues to rise. The prognosis of advanced melanoma remains poor, with median survival between 6 and 9 months. Over the past thirty years and despite extensive clinical research, the treatment options for metastatic disease were limited and melanoma is still considered as one of the most therapy-resistant malignancies. Single-agent and combination chemotherapy, hormonal therapy, biochemotherapy, immunotherapy, targeted agent therapy and combination regimes failed to show significant improvement in overall survival. Recent advances and in-depth understanding of the biology of melanoma, have contributed in the development of new agents. Based on the molecular and immunological background of the disease, the new drugs have shown benefit in overall and progression free survival. As the picture of the disease begins to change, oncologists need to alter their approach to melanoma treatment and consider disease biology together with targeted individualized treatment. In this review the authors attempt to offer an insight in present and past melanoma treatment options, with a focus on the recently approved immunotherapeutic agents and the clinical perspectives of these new weapons against metastatic melanoma. (C) 2013 Elsevier Ltd. All rights reserved.
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页码:879 / 885
页数:7
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