Immunotherapy in Melanoma

Author:

Saraceni Megan M.1,Khushalani Nikhil I.2,Jarkowski Anthony3

Affiliation:

1. Department of Pharmacy, University of Rochester Medical Center, Rochester, NY, USA

2. Roswell Park Cancer Institute, Buffalo, NY, USA

3. Department of Pharmacy, James P. Wilmot Cancer Center at the University of Rochester Medical Center, Rochester, NY, USA

Abstract

The incidence and mortality of melanoma are on the rise. Historically, patients diagnosed with metastatic melanoma were faced with a grim prognosis, with survival rates of 15% at 5 years. Prior to 2011, no drug or therapeutic regimen had been shown to improve overall survival (OS) in metastatic melanoma. Chemotherapeutic agents, such as dacarbazine or temozolomide, are often given to patients for palliative purposes; high-dose interleukin 2 and biochemotherapy are immunotherapeutic options that could be offered to patients with a good performance status at specialized centers. Neither has been shown to impact OS, but durable complete responses are seen in a minority of patients. Since 2011, 4 new drugs have been approved by the US Food and Drug Administration for the treatment of metastatic melanoma, all of which improve survival. Three of these agents (vemurafenib, dabrafenib, and trametinib) are targeted therapies, with ipilimumab being the only new immunotherapy. With a focus on immunotherapeutic agents, this review seeks to summarize the treatment options currently available for metastatic melanoma and to examine those on the near horizon.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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