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Analyzing the relationship between the efficacy of first-line immune checkpoint inhibitors and cumulative sun damage in Japanese patients with advanced BRAF wild-type nonacral cutaneous melanoma: A retrospective real-world, multicenter study.
Inozume, Takashi; Namikawa, Kenjiro; Kato, Hiroshi; Yoshikawa, Shusuke; Kiniwa, Yukiko; Yoshino, Koji; Mizuhashi, Satoru; Ito, Takamichi; Takenouchi, Tatsuya; Matsushita, Shigeto; Fujisawa, Yasuhiro; Matsuzawa, Takamitsu; Sugihara, Satoru; Asai, Jun; Kitagawa, Hiroshi; Maekawa, Takeo; Isei, Taiki; Yasuda, Masahito; Yamazaki, Naoya; Uhara, Hisashi; Nakamura, Yasuhiro.
Affiliation
  • Inozume T; Department of Dermatology, Chiba University, Chiba, Japan. Electronic address: tinozume@chiba-u.jp.
  • Namikawa K; Department of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Kato H; Department of Geriatric and Environmental Dermatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Yoshikawa S; Department of Dermatology, Shizuoka Cancer Center, Shizuoka, Japan.
  • Kiniwa Y; Department of Dermatology, Shinshu University, Matsumoto, Japan.
  • Yoshino K; Department of Skin Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Mizuhashi S; Department of Dermatology and Plastic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
  • Ito T; Department of Dermatology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Takenouchi T; Department of Dermatology, Niigata Cancer Center, Niigata, Japan.
  • Matsushita S; Department of Dermato-Oncology/Dermatology, National Hospital Organization Kagoshima Medical Center, Kagoshima, Japan.
  • Fujisawa Y; Department of Dermatology, University of Tsukuba, Ibaraki, Japan.
  • Matsuzawa T; Department of Dermatology, Chiba University, Chiba, Japan.
  • Sugihara S; Department of Dermatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Asai J; Department of Dermatology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Kitagawa H; Department of Dermatology, Mie University, Tsu, Japan.
  • Maekawa T; Department of Dermatology, Jichi Medical University, Tochigi, Japan.
  • Isei T; Department of Dermatological Oncology, Osaka International Cancer Institute, Osaka, Japan.
  • Yasuda M; Department of Dermatology, Gunma University Graduate School of Medicine, Gunma, Japan.
  • Yamazaki N; Department of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Uhara H; Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Nakamura Y; Department of Skin Oncology/Dermatology, Saitama Medical University International Medical Center, Saitama, Japan.
J Dermatol Sci ; 110(1): 19-26, 2023 Apr.
Article in En | MEDLINE | ID: mdl-37045720
ABSTRACT

BACKGROUND:

Efficacy of anti-PD-1 antibody monotherapy (PD1) or anti-PD-1 plus anti-CTLA-4 combination therapy (PD1 +CTLA4) for melanoma is affected by its clinical subtype. The amount of tumor mutation burden (TMB) caused by cumulative sun damage (CSD) is occasionally used to explain this; however, their relationship in Japanese nonacral cutaneous melanoma (NACM) is still unclear.

OBJECTIVE:

To analyze the ICI efficacy and its relationship with CSD of the primary lesion in Japanese patients with NACM.

METHODS:

Japanese patients with advanced BRAF wild-type NACM who received first-line ICIs were recruited. Objective response rate (ORR), progression-free survival (PFS), and overall survival (OS), and the degree of solar elastosis (SE) were evaluated.

RESULTS:

A total of 146 patients (PD1 group 113 and PD1 +CTLA4 group 33) were included. No significant differences in ORR were observed between the PD1 and PD1 +CTLA4 groups (35 % vs. 36 %; P = 0.67) or PFS and OS (median PFS 6.1 months vs. 8.5 months; P = 0.46, median OS 28.1 months vs. not reached; P = 0.59). Multivariate survival analysis revealed that PD1 +CTLA4 did not prolong the PFS and OS. The SE score had no effect on either PFS or OS.

CONCLUSIONS:

ICI efficacy was not as high as those reported in Western countries, and PD1 +CTLA4 did not present better clinical efficacy compared to PD1. Indicators of CSD did not serve as a predictor for clinical advantage. These findings may partially support the theory that ICI efficacy is affected by CSD; however, other unrecognized factors may also exist.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / Melanoma Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: J Dermatol Sci Journal subject: DERMATOLOGIA Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / Melanoma Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: J Dermatol Sci Journal subject: DERMATOLOGIA Year: 2023 Document type: Article