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Ipilimumab/Sargramostim Improves Overall Survival vs Ipilimumab Alone in Patients With Advanced Metastatic Melanoma

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Key Points

  • Median overall survival was 17.5 months for the ipilimumab-plus-sargramostim group vs 12.7 months for the ipilimumab-only group. Median progression-free survival was similar in both groups.
  • The 1-year overall survival rate for the ipilimumab-plus-sargramostim group was 68.9% compared to 52.9% for ipilimumab alone.
  • Grade 3 to 5 adverse events occurred more often in the ipilimumab-alone group (58.3% vs 44.9% in the combination group).

A randomized clinical trial of patients with advanced metastatic melanoma treated with ipilimumab (Yervoy), an immune checkpoint inhibitor, in combination with sargramostim (Leukine), an immune stimulant, vs ipilimumab alone, has found a 1-year survival rate of 68.9% vs 52.9% in the ipilimumab-only group. In addition, patients treated with the combination therapy experienced fewer serious adverse side effects than those treated with ipilimumab alone. The study by Hodi et al is published in the Journal of the American Medical Association.

Study Methodology

The Eastern Cooperative Oncology Group (ECOG) conducted a phase II randomized clinical from December 2010 to July 2011, enrolling 245 patients with stage III/IV metastatic melanoma who had received at least one prior therapy.

The patients were randomly assigned to receive ipilimumab plus sargramostim (granulocyte-macrophage colony-stimulating factor) vs ipilimumab alone. The primary end point was a comparison of length of overall survival. The secondary endpoint was progression-free survival, response rate, safety, and tolerability. The patients were followed for a median of 13.3 months.

Study Findings

The researchers found that the median overall survival for the ipilimumab-plus-sargramostim group was 17.5 months vs 12.7 months for the ipilimumab-only group. The 1-year survival rate for the combination therapy was 68.9% compared to 52.9% for ipilimumab alone (P = .01). In both groups, however, the median progression-free survival was similar, at 3.1 months. In addition, grade 3 to 5 adverse events occurred in 44.9% of patients in the ipilimumab-plus-sargramostim group vs 58.3% of patients in the ipilimumab-alone group.

“Among patients with unresectable stage III or IV melanoma, treatment with ipilimumab plus sargramostim vs ipilimumab alone resulted in longer [overall survival] and lower toxicity, but no difference in [progression-free survival]. These findings require confirmation in larger studies with longer follow-up,” concluded the researchers.

“This [study] opens the possibility of improving clinical outcomes and decreasing serious side effects in treating advanced melanoma with ipilimumab,” said F. Stephen Hodi, MD, Director of the Melanoma Treatment Center and Director of the Center for Immuno-Oncology at Dana-Farber Cancer Institute and first author of the study, in a statement.

The research was supported by Public Health Service Grants, the National Cancer Institute, National Institutes of Health, and the Department of Health and Human Services.

The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.


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