Safety and efficacy of nivolumab in patients with rare melanoma subtypes who progressed on or after ipilimumab treatment: a single-arm, open-label, phase II study (CheckMate 172)

Nivolumab has been widely studied in non-acral cutaneous melanoma; however, limited data are available in other melanoma subtypes. We report outcomes by melanoma subtype in patients who received nivolumab after progression on prior ipilimumab. CheckMate 172 was a phase II, single-arm, open-label, mu...

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Veröffentlicht in:European journal of cancer (1990) 2019-09, Vol.119, p.168-178
Hauptverfasser: Nathan, Paul, Ascierto, Paolo A., Haanen, John, Espinosa, Enrique, Demidov, Lev, Garbe, Claus, Guida, Michele, Lorigan, Paul, Chiarion-Sileni, Vanna, Gogas, Helen, Maio, Michele, Fierro, Maria Teresa, Hoeller, Christoph, Terheyden, Patrick, Gutzmer, Ralf, Guren, Tormod K., Bafaloukos, Dimitrios, Rutkowski, Piotr, Plummer, Ruth, Waterston, Ashita, Kaatz, Martin, Mandala, Mario, Marquez-Rodas, Ivan, Muñoz-Couselo, Eva, Dummer, Reinhard, Grigoryeva, Elena, Young, Tina C., Schadendorf, Dirk
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Sprache:eng
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Zusammenfassung:Nivolumab has been widely studied in non-acral cutaneous melanoma; however, limited data are available in other melanoma subtypes. We report outcomes by melanoma subtype in patients who received nivolumab after progression on prior ipilimumab. CheckMate 172 was a phase II, single-arm, open-label, multicentre study that evaluated nivolumab in patients with advanced melanoma who progressed on or after ipilimumab. Patients received 3 mg/kg of nivolumab, every 2 weeks for up to 2 years. The primary end-point was incidence of grade ≥3, treatment-related select adverse events (AEs). Among 1008 treated patients, we report data on patients with non-acral cutaneous melanoma (n = 723 [71.7%]), ocular melanoma (n = 103 [10.2%]), mucosal melanoma (n = 63 [6.3%]), acral cutaneous melanoma (n = 55 [5.5%]) and other melanoma subtypes (n = 64 [6.3%]). There were no meaningful differences in the incidence of grade ≥3, treatment-related select AEs among melanoma subtypes or compared with the total population. No new safety signals emerged. At a minimum follow-up of 18 months, median overall survival was 25.3 months for non-acral cutaneous melanoma and 25.8 months for acral cutaneous melanoma, with 18-month overall survival rates of 57.5% and 59.0%, respectively. Median overall survival was 12.6 months for ocular melanoma and 11.5 months for mucosal melanoma, with 18-month overall survival rates of 34.8% and 31.5%, respectively. The safety profile of nivolumab after ipilimumab is similar across melanoma subtypes. Compared with non-acral cutaneous melanoma, patients with acral cutaneous melanoma had similar survival outcomes, whereas those with ocular and mucosal melanoma had lower median overall survival. : NCT02156804. •The safety profile for nivolumab was similar across melanoma subtypes.•Survival was similar in non-acral cutaneous and acral cutaneous melanoma subtypes.•Median overall survival was lowest in patients with ocular and mucosal melanoma.
ISSN:0959-8049
1879-0852
DOI:10.1016/j.ejca.2019.07.010