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Five‐year survival with nivolumab in previously untreated Japanese patients with advanced or recurrent malignant melanoma

We report the 5‐year follow‐up results from a single‐arm, open‐label, multicenter phase II study (ONO‐4538‐08) conducted in Japan. Twenty‐four patients with treatment‐naïve, recurrent, or unresectable stage III/IV malignant melanoma received 3 mg/kg nivolumab every 2 weeks until progressive disease...

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Autores principales: Uhara, Hisashi, Kiyohara, Yoshio, Uehara, Jiro, Fujisawa, Yasuhiro, Takenouchi, Tatsuya, Otsuka, Masaki, Uchi, Hiroshi, Fukushima, Satoshi, Minami, Hironobu, Hatsumichi, Masahiro, Yamazaki, Naoya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252056/
https://www.ncbi.nlm.nih.gov/pubmed/33715172
http://dx.doi.org/10.1111/1346-8138.15804
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author Uhara, Hisashi
Kiyohara, Yoshio
Uehara, Jiro
Fujisawa, Yasuhiro
Takenouchi, Tatsuya
Otsuka, Masaki
Uchi, Hiroshi
Fukushima, Satoshi
Minami, Hironobu
Hatsumichi, Masahiro
Yamazaki, Naoya
author_facet Uhara, Hisashi
Kiyohara, Yoshio
Uehara, Jiro
Fujisawa, Yasuhiro
Takenouchi, Tatsuya
Otsuka, Masaki
Uchi, Hiroshi
Fukushima, Satoshi
Minami, Hironobu
Hatsumichi, Masahiro
Yamazaki, Naoya
author_sort Uhara, Hisashi
collection PubMed
description We report the 5‐year follow‐up results from a single‐arm, open‐label, multicenter phase II study (ONO‐4538‐08) conducted in Japan. Twenty‐four patients with treatment‐naïve, recurrent, or unresectable stage III/IV malignant melanoma received 3 mg/kg nivolumab every 2 weeks until progressive disease or unacceptable toxicity occurred. The 5‐year overall survival (OS) rate was 26.1%. Five years after the start of nivolumab treatment, there were six survivors. The 5‐year OS rate was 66.7% for patients with a superficial spreading type, 14.3% for acral lentiginous type, and 16.7% for mucosal type. The 5‐year progression‐free survival rate was 17.2%. No new cases of partial response or complete response were observed after 3 years, and overall response and disease control rates were similar to those reported at 3 years. The treatment‐related adverse events reported between the 3‐ and 5‐year follow‐up periods were anemia (grade 2), white blood cell count decrease (grade 2), and psoriasiform dermatitis (grade 2) in one patient each. No new grade 3 or higher treatment‐related adverse events occurred in this period. In conclusion, first‐line treatment with nivolumab in Japanese patients with unresectable or metastatic melanoma resulted in confirmed long‐term survival. No new safety signals were reported in the studied population.
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spelling pubmed-82520562021-07-07 Five‐year survival with nivolumab in previously untreated Japanese patients with advanced or recurrent malignant melanoma Uhara, Hisashi Kiyohara, Yoshio Uehara, Jiro Fujisawa, Yasuhiro Takenouchi, Tatsuya Otsuka, Masaki Uchi, Hiroshi Fukushima, Satoshi Minami, Hironobu Hatsumichi, Masahiro Yamazaki, Naoya J Dermatol Original Articles We report the 5‐year follow‐up results from a single‐arm, open‐label, multicenter phase II study (ONO‐4538‐08) conducted in Japan. Twenty‐four patients with treatment‐naïve, recurrent, or unresectable stage III/IV malignant melanoma received 3 mg/kg nivolumab every 2 weeks until progressive disease or unacceptable toxicity occurred. The 5‐year overall survival (OS) rate was 26.1%. Five years after the start of nivolumab treatment, there were six survivors. The 5‐year OS rate was 66.7% for patients with a superficial spreading type, 14.3% for acral lentiginous type, and 16.7% for mucosal type. The 5‐year progression‐free survival rate was 17.2%. No new cases of partial response or complete response were observed after 3 years, and overall response and disease control rates were similar to those reported at 3 years. The treatment‐related adverse events reported between the 3‐ and 5‐year follow‐up periods were anemia (grade 2), white blood cell count decrease (grade 2), and psoriasiform dermatitis (grade 2) in one patient each. No new grade 3 or higher treatment‐related adverse events occurred in this period. In conclusion, first‐line treatment with nivolumab in Japanese patients with unresectable or metastatic melanoma resulted in confirmed long‐term survival. No new safety signals were reported in the studied population. John Wiley and Sons Inc. 2021-03-14 2021-05 /pmc/articles/PMC8252056/ /pubmed/33715172 http://dx.doi.org/10.1111/1346-8138.15804 Text en © 2021 The Authors. The Journal of Dermatology published by John Wiley & Sons Australia, Ltd on behalf of Japanese Dermatological Association. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Uhara, Hisashi
Kiyohara, Yoshio
Uehara, Jiro
Fujisawa, Yasuhiro
Takenouchi, Tatsuya
Otsuka, Masaki
Uchi, Hiroshi
Fukushima, Satoshi
Minami, Hironobu
Hatsumichi, Masahiro
Yamazaki, Naoya
Five‐year survival with nivolumab in previously untreated Japanese patients with advanced or recurrent malignant melanoma
title Five‐year survival with nivolumab in previously untreated Japanese patients with advanced or recurrent malignant melanoma
title_full Five‐year survival with nivolumab in previously untreated Japanese patients with advanced or recurrent malignant melanoma
title_fullStr Five‐year survival with nivolumab in previously untreated Japanese patients with advanced or recurrent malignant melanoma
title_full_unstemmed Five‐year survival with nivolumab in previously untreated Japanese patients with advanced or recurrent malignant melanoma
title_short Five‐year survival with nivolumab in previously untreated Japanese patients with advanced or recurrent malignant melanoma
title_sort five‐year survival with nivolumab in previously untreated japanese patients with advanced or recurrent malignant melanoma
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252056/
https://www.ncbi.nlm.nih.gov/pubmed/33715172
http://dx.doi.org/10.1111/1346-8138.15804
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