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DOI 10.1200/jco.22.00533

Медицинская библиотека · Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022

Adjuvant Therapy of Nivolumab Combined With Ipilimumab Versus Nivolumab Alone in Patients With Resected Stage IIIB-D or Stage IV Melanoma (CheckMate 915).

Weber Jeffrey S, Schadendorf Dirk, Del Vecchio Michele, Larkin James, Atkinson Victoria, Schenker Michael, Pigozzo Jacopo, Gogas Helen, Dalle Stéphane, Meyer Nicolas, Ascierto Paolo A, Sandhu Shahneen, Eigentler Thomas, Gutzmer Ralf, Hassel Jessica C, Robert Caroline, Carlino Matteo S, Di Giacomo Anna Maria, Butler Marcus O, Muñoz-Couselo Eva, Brown Michael P, Rutkowski Piotr, Haydon Andrew, Grob Jean-Jacques, Schachter Jacob, Queirolo Paola, de la Cruz-Merino Luis, van der Westhuizen Andre, Menzies Alexander M, Re Sandra, Bas Tuba, de Pril Veerle, Braverman Julia, Tenney Daniel J, Tang Hao, Long Georgina V

Клиническое исследование III фазыСтатьяРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

PURPOSE: Ipilimumab and nivolumab have each shown treatment benefit for high-risk resected melanoma. The phase III CheckMate 915 trial evaluated adjuvant nivolumab plus ipilimumab versus nivolumab alone in patients with resected stage IIIB-D or IV melanoma.

PATIENTS AND

METHODS

In this randomized, double-blind, phase III trial, 1,833 patients received nivolumab 240 mg once every 2 weeks plus ipilimumab 1 mg/kg once every 6 weeks (916 patients) or nivolumab 480 mg once every 4 weeks (917 patients) for ≤ 1 year. After random assignment, patients were stratified by tumor programmed death ligand 1 (PD-L1) expression and stage. Dual primary end points were recurrence-free survival (RFS) in randomly assigned patients and in the tumor PD-L1 expression-level < 1% subgroup.

RESULTS

At a minimum follow-up of approximately 23.7 months, there was no significant difference between treatment groups for RFS in the all-randomly assigned patient population (hazard ratio, 0.92; 95% CI, 0.77 to 1.09; P = .269) or in patients with PD-L1 expression < 1% (hazard ratio, 0.91; 95% CI, 0.73 to 1.14). In all patients, 24-month RFS rates were 64.6% (combination) and 63.2% (nivolumab). Treatment-related grade 3 or 4 adverse events were reported in 32.6% of patients in the combination group and 12.8% in the nivolumab group. Treatment-related deaths were reported in 0.4% of patients in the combination group and in no nivolumab-treated patients.

CONCLUSION

Nivolumab 240 mg once every 2 weeks plus ipilimumab 1 mg/kg once every 6 weeks did not improve RFS versus nivolumab 480 mg once every 4 weeks in patients with stage IIIB-D or stage IV melanoma. Nivolumab showed efficacy consistent with previous adjuvant studies in a population resembling current practice using American Joint Committee on Cancer eighth edition, reaffirming nivolumab as a standard of care for melanoma adjuvant treatment.

Для цитирования: Weber Jeffrey S, Schadendorf Dirk, Del Vecchio Michele, Larkin James, Atkinson Victoria, Schenker Michael, Pigozzo Jacopo, Gogas Helen, Dalle Stéphane, Meyer Nicolas, Ascierto Paolo A, Sandhu Shahneen, Eigentler Thomas, Gutzmer Ralf, Hassel Jessica C, Robert Caroline, Carlino Matteo S, Di Giacomo Anna Maria, Butler Marcus O, Muñoz-Couselo Eva, Brown Michael P, Rutkowski Piotr, Haydon Andrew, Grob Jean-Jacques, Schachter Jacob, Queirolo Paola, de la Cruz-Merino Luis, van der Westhuizen Andre, Menzies Alexander M, Re Sandra, Bas Tuba, de Pril Veerle, Braverman Julia, Tenney Daniel J, Tang Hao, Long Georgina V. Adjuvant Therapy of Nivolumab Combined With Ipilimumab Versus Nivolumab Alone in Patients With Resected Stage IIIB-D or Stage IV Melanoma (CheckMate 915).. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2022. DOI: 10.1200/jco.22.00533.

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