Final analysis of a phase II study of nivolumab in combination with ipilimumab for unresectable chemotherapy-naive advanced melanoma.


Journal

The Journal of dermatology
ISSN: 1346-8138
Titre abrégé: J Dermatol
Pays: England
ID NLM: 7600545

Informations de publication

Date de publication:
Nov 2020
Historique:
received: 15 05 2020
accepted: 18 06 2020
pubmed: 20 8 2020
medline: 15 5 2021
entrez: 20 8 2020
Statut: ppublish

Résumé

Nivolumab plus ipilimumab combination is currently one of the preferred regimens for advanced melanoma in recently updated clinical practice guidelines. However, the evidence on the efficacy of the combination for acral or mucosal subtypes remains less robust. This is the final analysis of a multicenter, open-label, uncontrolled phase II study that investigated the long-term efficacy and safety in treatment-naive Japanese patients with advanced melanoma, including acral or mucosal subtypes, and subsequent therapy after discontinuation of the investigational agents. Patients received four doses of nivolumab (1 mg/kg i.v.) in combination with ipilimumab (3 mg/kg i.v.) at 3-week intervals, followed by doses of nivolumab (3 mg/kg i.v.) at 2-week intervals. The median follow-up period was 20.8 months (range, 5.2-35.0). The centrally and locally assessed objective response rates were both 43.3% (13/30; 95% confidence interval [CI], 25.5-62.6). Median progression-free survival was not reached (95% CI, 3.02-not reached), and median overall survival was also not reached (95% CI, 19.52-not reached). The 30-month progression-free survival and overall survival rates were 50.3% and 54.2%, respectively. No new safety concerns were detected. After discontinuation of the investigational agents, 83.3% of patients received some form of subsequent therapy including 43.3% of patients who received nivolumab monotherapy and 26.7% of patients who received radiotherapy. Of the four patients who discontinued the investigational agents because of immune-related adverse events, two received subsequent therapy (nivolumab and ipilimumab, respectively) and the other two showed long-term treatment-free survival (659 and 590 days, respectively). Long-term survival with nivolumab plus ipilimumab was observed in Japanese patients with melanoma including acral and mucosal subtypes, which is consistent with the CheckMate 067 study. Many patients continued to receive some form of treatment safely after stopping treatment with nivolumab plus ipilimumab.

Identifiants

pubmed: 32812243
doi: 10.1111/1346-8138.15514
pmc: PMC7693067
doi:

Substances chimiques

Ipilimumab 0
Nivolumab 31YO63LBSN

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1257-1266

Subventions

Organisme : Ono Pharmaceutical Co., Ltd.
ID : N/A
Organisme : Bristol Myers Squibb
ID : N/A

Informations de copyright

© 2020 The Authors. The Journal of Dermatology published by John Wiley & Sons Australia, Ltd on behalf of Japanese Dermatological Association.

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Auteurs

Kenjiro Namikawa (K)

Department of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.

Yoshio Kiyohara (Y)

Dermatology Division, Shizuoka Cancer Center Hospital, Shizuoka, Japan.

Tatsuya Takenouchi (T)

Department of Dermatology, Niigata Cancer Center Hospital, Niigata, Japan.

Hisashi Uhara (H)

Department of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan.

Hiroshi Uchi (H)

Department of Dermatology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Shusuke Yoshikawa (S)

Dermatology Division, Shizuoka Cancer Center Hospital, Shizuoka, Japan.

Sumiko Takatsuka (S)

Department of Dermatology, Niigata Cancer Center Hospital, Niigata, Japan.

Hiroshi Koga (H)

Department of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan.

Naoko Wada (N)

Department of Dermatology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Hironobu Minami (H)

Department of Medical Oncology/Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.

Masahiro Hatsumichi (M)

Ono Pharmaceutical Co., Ltd., Osaka, Japan.

Yoshinobu Namba (Y)

Ono Pharmaceutical Co., Ltd., Osaka, Japan.

Naoya Yamazaki (N)

Department of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.

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