Alexander M M Eggermont1, Vanna Chiarion-Sileni2, Jean-Jacques Grob3, Reinhard Dummer4, Jedd D Wolchok5, Henrik Schmidt6, Omid Hamid7, Caroline Robert8, Paolo Antonio Ascierto9, Jon M Richards10, Celeste Lebbe11, Virginia Ferraresi12, Michael Smylie13, Jeffrey S Weber14, Michele Maio15, Fareeda Hosein16, Veerle de Pril17, Michal Kicinski18, Stefan Suciu18, Alessandro Testori19. 1. Gustave Roussy Cancer Insitute and University Paris-Sud, France. Electronic address: alexander.eggermont@gustaveroussy.fr. 2. Veneto Institute of Oncology IOV-IRCCS, Padua, Italy. 3. AIX-Marseille University, Marseille, France. 4. University of Zurich Hospital, Zurich, Switzerland. 5. Memorial Sloan Kettering Cancer Center, New York, NY, USA. 6. Aarhus University Hospital, Aarhus, Denmark. 7. The Angeles Clinic and Research Institute, Los Angeles, CA, USA. 8. Melanoma Department, Gustave Roussy Institute and Univerity Paris-Sud, France. 9. Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale", Naples, Italy. 10. Oncology Specialists, SC, Park Ridge, IL, USA. 11. Dermatology and CIC Department, AP-HP, Saint-Louis Hospital, Université de Paris, INSERM U976, Paris, France. 12. Regina Elena National Cancer Institute, Rome, Italy. 13. Cross Cancer Institute, Edmonton, AB, Canada. 14. New York University Perlmutter Cancer Center, New York, NY, USA. 15. Center for Immuno-Oncology, University Hospital of Siena, Siena, Italy. 16. Bristol-Myers Squibb, Lawrenceville, NJ, USA. 17. Bristol-Myers Squibb, Braine-L'alleud, Belgium. 18. EORTC Headquarters, Brussels, Belgium. 19. Formerly at European Institute of Oncology, Milan, Italy.
Abstract
BACKGROUND: Since 2015, adjuvant therapy with ipilimumab is an approved treatment for stage III melanoma based on a significantly prolonged recurrence-free survival (RFS). At a median follow-up of 5.3 years, RFS, distant metastasis-free survival (DMFS) and overall survival (OS) were each significantly prolonged in the ipilimumab group compared with the placebo group, despite a 53.3% (ipilimumab) versus 4.6% (placebo) treatment discontinuation rate due to adverse events. We present now long-term follow-up results of this European Organisation for Research and Treatment of Cancer 18071 trial. PATIENTS, METHODS AND RESULTS:A total of 99 sites randomised 951 patients with stage III cutaneous melanoma (excluding lymph node metastasis ≤1 mm or in-transit metastasis) with adequate resection of lymph nodes to receiveintravenous infusions of ipilimumab 10 mg/kg or placebo, every 3 weeks for 4 doses, then every 3 months for up to 3 years. The RFS, DMFS and OS, as reported by the local investigators, were assessed by the intention-to-treat analysis. Among 431 patients randomised at 63 sites and who were still alive at the analysis reported in 2016, recent follow-up information could be obtained for 264 patients. The median OS follow-up was 6.9 years. The RFS (hazard ratio [HR] 0.75, 95% confidence interval 0.63-0.88; P < 0.001), DMFS (HR 0.76, 0.64-0.90; P = 0.002) and OS (HR 0.73, 0.60-0.89; P = 0.002) benefit observed in the ipilimumab group was durable with an 8.7% absolute difference at 7 years for OS. The benefit was consistent across subgroups. CONCLUSIONS: Adjuvant therapy with ipilimumab prolongs RFS, DMFS and OS significantly. The benefit is sustained long term and consistent across subgroups.
RCT Entities:
BACKGROUND: Since 2015, adjuvant therapy with ipilimumab is an approved treatment for stage III melanoma based on a significantly prolonged recurrence-free survival (RFS). At a median follow-up of 5.3 years, RFS, distant metastasis-free survival (DMFS) and overall survival (OS) were each significantly prolonged in the ipilimumab group compared with the placebo group, despite a 53.3% (ipilimumab) versus 4.6% (placebo) treatment discontinuation rate due to adverse events. We present now long-term follow-up results of this European Organisation for Research and Treatment of Cancer 18071 trial. PATIENTS, METHODS AND RESULTS: A total of 99 sites randomised 951 patients with stage III cutaneous melanoma (excluding lymph node metastasis ≤1 mm or in-transit metastasis) with adequate resection of lymph nodes to receive intravenous infusions of ipilimumab 10 mg/kg or placebo, every 3 weeks for 4 doses, then every 3 months for up to 3 years. The RFS, DMFS and OS, as reported by the local investigators, were assessed by the intention-to-treat analysis. Among 431 patients randomised at 63 sites and who were still alive at the analysis reported in 2016, recent follow-up information could be obtained for 264 patients. The median OS follow-up was 6.9 years. The RFS (hazard ratio [HR] 0.75, 95% confidence interval 0.63-0.88; P < 0.001), DMFS (HR 0.76, 0.64-0.90; P = 0.002) and OS (HR 0.73, 0.60-0.89; P = 0.002) benefit observed in the ipilimumab group was durable with an 8.7% absolute difference at 7 years for OS. The benefit was consistent across subgroups. CONCLUSIONS: Adjuvant therapy with ipilimumab prolongs RFS, DMFS and OS significantly. The benefit is sustained long term and consistent across subgroups.
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