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Clinical Trial
. 2015 Apr 1;33(10):1191-6.
doi: 10.1200/JCO.2014.56.6018. Epub 2015 Feb 23.

Five-year survival rates for treatment-naive patients with advanced melanoma who received ipilimumab plus dacarbazine in a phase III trial

Affiliations
Clinical Trial

Five-year survival rates for treatment-naive patients with advanced melanoma who received ipilimumab plus dacarbazine in a phase III trial

Michele Maio et al. J Clin Oncol. .

Abstract

Purpose: There is evidence from nonrandomized studies that a proportion of ipilimumab-treated patients with advanced melanoma experience long-term survival. To demonstrate a long-term survival benefit with ipilimumab, we evaluated the 5-year survival rates of patients treated in a randomized, controlled phase III trial.

Patients and methods: A milestone survival analysis was conducted to capture the 5-year survival rate of treatment-naive patients with advanced melanoma who received ipilimumab in a phase III trial. Patients were randomly assigned 1:1 to receive ipilimumab at 10 mg/kg plus dacarbazine (n = 250) or placebo plus dacarbazine (n = 252) at weeks 1, 4, 7, and 10 followed by dacarbazine alone every 3 weeks through week 22. Eligible patients could receive maintenance ipilimumab or placebo every 12 weeks beginning at week 24. A safety analysis was conducted on patients who survived at least 5 years and continued to receive ipilimumab as maintenance therapy.

Results: The 5-year survival rate was 18.2% (95% CI, 13.6% to 23.4%) for patients treated with ipilimumab plus dacarbazine versus 8.8% (95% CI, 5.7% to 12.8%) for patients treated with placebo plus dacarbazine (P = .002). A plateau in the survival curve began at approximately 3 years. In patients who survived at least 5 years and continued to receive ipilimumab, grade 3 or 4 immune-related adverse events were observed exclusively in the skin.

Conclusion: The additional survival benefit of ipilimumab plus dacarbazine is maintained with twice as many patients alive at 5 years compared with those who initially received placebo plus dacarbazine. These results demonstrate a durable survival benefit with ipilimumab in advanced melanoma.

Trial registration: ClinicalTrials.gov NCT00324155.

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Conflict of interest statement

Authors' disclosures of potential conflicts of interest are found in the article online at www.jco.org. Author contributions are found at the end of this article.

Figures

Fig 1.
Fig 1.
CONSORT diagram. DTIC, dacarbazine.
Fig 2.
Fig 2.
Kaplan-Meier estimates of overall survival in patients treated with ipilimumab plus dacarbazine (DTIC) or placebo plus DTIC in phase III CA184-024 study. Symbols indicate censored observations. Red box highlights updated 5-year survival data.

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References

    1. Garbe C Eigentler TK Keilholz U , etal: Systematic review of medical treatment in melanoma: Current status and future prospects Oncologist 16: 5– 24,2011. - PMC - PubMed
    1. Hodi FS O'Day SJ McDermott DF , etal: Improved survival with ipilimumab in patients with metastatic melanoma N Engl J Med 363: 711– 723,2010. - PMC - PubMed
    1. Robert C Thomas L Bondarenko I , etal: Ipilimumab plus dacarbazine for previously untreated metastatic melanoma N Engl J Med 364: 2517– 2526,2011. - PubMed
    1. Luke JJ, Hodi FS: Ipilimumab, vemurafenib, dabrafenib, and trametinib: Synergistic competitors in the clinical management of BRAF mutant malignant melanoma Oncologist 18: 717– 725,2013. - PMC - PubMed
    1. Hoos A Ibrahim R Korman A , etal: Development of ipilimumab: Contribution to a new paradigm for cancer immunotherapy Semin Oncol 37: 533– 546,2010. - PubMed

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