Anti-CTLA-4 Antibody Adjuvant Therapy in Melanoma

被引:32
作者
Eggermont, Alexander M. M. [1 ]
Testori, Alessandro [2 ]
Maio, Michele [3 ]
Robert, Caroline [4 ]
机构
[1] Inst Oncol Gustave Roussy, F-94805 Villejuif, France
[2] European Inst Oncol, Div Melanoma, Milan, Italy
[3] Univ Hosp Siena, Dept Oncol, Siena, Italy
[4] Inst Gustave Roussy, Dermatol Unit, Villejuif, France
关键词
HIGH-RISK MELANOMA; COLONY-STIMULATING FACTOR; PHASE-III TRIAL; INTERFERON ALPHA-2A; METASTATIC MELANOMA; DOSE INTERFERON-ALPHA-2B; CUTANEOUS MELANOMA; RANDOMIZED-TRIAL; VACCINE; IMMUNOTHERAPY;
D O I
10.1053/j.seminoncol.2010.09.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Thus far the development of adjuvant therapies in melanoma has suffered greatly from the lack of effective drugs in stage IV melanoma. Chemotherapy, cytokines, vaccines, and combinations of drugs have been used with minimal success. This has led to adjuvant therapies that are not used uniformly or widely because of the rather marginal benefits, as no consistent and clinically significant impact on survival has been demonstrated. A new development for interferon-based adjuvant therapy seems to be the observation that better effects are observed in patients with lower tumor load and in patients with an ulcerated primary melanoma. A benefit for patients with more advanced lymphnodal involvement is quite unsure, clearly requiring new drugs to be explored. A new era in the treatment of melanoma treatment has arrived with the anti- cytoxic T-lymphocyte antigen-4 (anti-CTLA-4) monoclonal antibodies. The randomized trial in advanced metastatic melanoma demonstrated a clear benefit with prolongation of survival. The anti-CTLA-4 monoclonal antibody ipilimumab has finally changed the landscape. It is therefore only logical that a worldwide adjuvant trial with ipilimumab versus placebo, the European Organization for Research and Treatment of Cancer (EORTC) 18071, is ongoing in patients with lymph node metastases, and that another adjuvant trial with ipilimumab compared to high-dose interferon (HDI) is planned in the United States. The EORTC 18071 trial will reach full accrual in 2011 and thus results are expected in 2013 or 2014. Semin Oncol 37:455-459 (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:455 / 459
页数:5
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