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Nivolumab and Ipilimumab versus Ipilimumab in Untreated Melanoma
Nivolumab and Ipilimumab versus Ipilimumab in Untreated Melanoma
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Nivolumab and Ipilimumab versus Ipilimumab in Untreated Melanoma
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Nivolumab and Ipilimumab versus Ipilimumab in Untreated Melanoma
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Nivolumab and Ipilimumab versus Ipilimumab in Untreated Melanoma
Nivolumab and Ipilimumab versus Ipilimumab in Untreated Melanoma
Journal Article

Nivolumab and Ipilimumab versus Ipilimumab in Untreated Melanoma

2015
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Overview
The combination of a CTLA-4 blocker and a PD-1 blocker produced responses in more than 60% of previously untreated patients with BRAF wild-type advanced melanoma, including complete responses in more than 20% of these patients. Recent approaches to the treatment of metastatic melanoma enhance antitumor immunity by blocking immune checkpoints, such as cytotoxic T-lymphocyte–associated antigen 4 (CTLA-4) and the programmed death 1 (PD-1) receptor. Ipilimumab, an anti–CTLA-4 antibody, is approved by the Food and Drug Administration (FDA) on the basis of improvement in overall survival among patients with advanced melanoma, with objective responses in approximately 11% of the patients. 1 , 2 Nivolumab, an anti–PD-1 monoclonal antibody, has recently been shown to improve overall survival, as compared with dacarbazine (objective response rate, 40% vs. 14%), among previously untreated patients with advanced BRAF wild-type melanoma. 3 Nivolumab is approved . . .