Secondary Logo

Journal Logo

Opdivo-Yervoy Combination Approved for Melanoma—First Combination-Immunotherapy Regimen for Cancer

doi: 10.1097/01.COT.0000473604.35674.ee
FDA Updates
Free
Figure

Figure

The U.S. Food and Drug Administration has approved Opdivo (nivolumab) in combination with Yervoy (ipilimumab) for the treatment of patients with BRAF V600 wild-type unresectable or metastatic melanoma. Opdivo is a PD-1 checkpoint inhibitor and Yervoy is a CTLA-4 checkpoint inhibitor. This approval is the first approval of a combination regimen of two immuno-oncology agents for the treatment of cancer.

“Historically, metastatic melanoma has been a difficult disease to treat. Now, a new treatment option based on the combination of two valued immuno-oncology agents demonstrates significant efficacy versus ipilimumab (Yervoy) in metastatic melanoma,” Jedd D. Wolchok, MD, PhD, Chief of the Melanoma and Immunotherapeutics Service in the Department of Medicine and at the Ludwig Center at Memorial Sloan Kettering Cancer Center, said in a news release.

“The approval represents a step forward for the melanoma community, providing hope for patients with metastatic melanoma.”

The Opdivo-Yervoy combination was approved under the FDA's accelerated approval program, which allows approval of a drug to treat a serious or life-threatening disease based on clinical data showing that the drug has an effect on a surrogate endpoint reasonably likely to predict clinical benefit to patients. This program provides earlier patient access to promising new drugs while the company conducts confirmatory clinical trials.

Back to Top | Article Outline

Safety and Efficacy

Safety and efficacy for the Opdivo-Yervoy combination were established in the Phase II, double-blind CheckMate-069 trial of 142 patients with previously untreated unresectable or metastatic melanoma who were randomized to receive Opdivo with Yervoy or Yervoy alone (OT 6/10/15 issue). Median progression free survival for the patients with BRAF wild-type melanoma was 8.9 months for patients receiving the combination compared with 4.7 months for patients receiving Yervoy alone.

Serious adverse reactions were more common in the patients receiving the combination regimen than for patients receiving Yervoy alone. The most common serious adverse reactions associated with the combination regimen were colitis, diarrhea, pyrexia, and pneumonitis. Other common adverse reactions for patients receiving the combination therapy were rash, pruritus, headache, vomiting, and colitis.

Back to Top | Article Outline

Responses from the Oncology Community

The approval was applauded by the Melanoma Research Foundation in a statement from Tim Turnham, the organization's Executive Director: “The approval marks a turning point in melanoma treatment. For the first time patients will have access to a regimen that utilizes two critical findings—that the patient's own immune system can be engaged in the fight against cancer, and that the right combination of two or more drugs can have a synergistic effect.”

The decision was also praised by the Society for Immunotherapy of Cancer. SITC President Howard L. Kaufman, MD, FACS, of Rutgers Cancer Institute of New Jersey said: “Today marks a milestone in the field of cancer immunotherapy. ... Not only does this combination immunotherapy demonstrate an impressive, durable response in patients with metastatic melanoma, but the approval also illustrates the potential advantage of combining immunotherapy agents offering previously unavailable options to cancer patients.”

Both drugs are marketed by Bristol-Myers Squibb.

Back to Top | Article Outline

Clinical Quick Facts: Opdivo-Yervoy

Drug: Opdivo (nivolumab) in combination with Yervoy (ipilimumab)

Approved Indication: Treatment of patients with BRAF V600 wild-type unresectable or metastatic melanoma

Serious Side Effects: Colitis, diarrhea, pyrexia, and pneumonitis

Common Side Effects: Rash, pruritus, headache, vomiting, and colitis

Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved.
Home  Clinical Resource Center
Current Issue       Search OT
Archives Get OT Enews
Blogs Email us!