| Literature DB >> 27510892 |
Yasuhiro Nakamura1, Ryota Tanaka2, Yuri Asami1, Yukiko Teramoto1, Taichi Imamura1, Sayuri Sato1, Hiroshi Maruyama2, Yasuhiro Fujisawa2, Taisuke Matsuya1, Manabu Fujimoto2, Akifumi Yamamoto1.
Abstract
Vitiligo is occasionally seen in melanoma patients. Although several studies indicate a correlation between vitiligo occurrence and clinical response in melanoma patients receiving immunotherapy, most studies have included heterogeneous patient and treatment settings. The aim of this study is to investigate the correlation between the occurrence of vitiligo and clinical benefit of nivolumab treatment in advanced melanoma patients. We retrospectively reviewed unresectable stage III or IV melanoma patients treated with nivolumab. Of 35 melanoma patients treated with nivolumab, 25.7% (9/35) developed vitiligo during treatment. The time from the start of nivolumab treatment to occurrence of vitiligo ranged 2-9 months (mean, 5.2). Of nine patients who developed vitiligo, two (22.2%) had a complete response to nivolumab and two (22.2%) had a partial response. The objective response rate was significantly higher in patients with vitiligo than in patients without vitiligo (4/9 [44.4%] vs 2/26 [7.7%]; P = 0.027). The mean time to vitiligo occurrence in patients achieving an objective response was significantly less than that in patients who showed no response (3.1 vs 6.8 months, P = 0.004). Vitiligo occurrence was significantly associated with prolonged progression-free and overall survival (hazard ratio, 0.24 and 0.16; 95% confidence interval, 0.11-0.55 and 0.03-0.79; P = 0.005, and 0.047, respectively). At the 20-week landmark analysis, however, vitiligo was not associated with a statistically significant overall survival benefit (P = 0.28). The occurrence of vitiligo during nivolumab treatment may be correlated with favorable clinical outcome.Entities:
Keywords: immune-related adverse events; melanoma; nivolumab; programmed death receptor-1; vitiligo
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Year: 2016 PMID: 27510892 DOI: 10.1111/1346-8138.13520
Source DB: PubMed Journal: J Dermatol ISSN: 0385-2407 Impact factor: 4.005