Hansje-Eva Teulings, Jacqueline Limpens, Sophia N. Jansen, Aeilko H. Zwinderman, Johannes B. Reitsma, Phyllis I. Spuls, and Rosalie M. Luiten, Academic Medical Centre, University of Amsterdam, Amsterdam; Johannes B. Reitsma, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands.
J Clin Oncol. 2015 Mar 1;33(7):773-81. doi: 10.1200/JCO.2014.57.4756. Epub 2015 Jan 20.
Vitiligo-like depigmentation in patients with melanoma may be associated with more favorable clinical outcome. We conducted a systematic review of patients with stage III to IV melanoma treated with immunotherapy to determine the cumulative incidence of vitiligo-like depigmentation and the prognostic value of vitiligo development on survival.
We systemically searched and selected all studies on melanoma immunotherapy that reported on autoimmune toxicity and/or vitiligo between 1995 and 2013. Methodologic quality of each study was appraised using adapted criteria for systematic reviews in prognostic studies. Random-effect models were used to calculate summary estimates of the cumulative incidence of vitiligo-like depigmentation across studies. The prognostic value of vitiligo-like depigmentation on survival outcome was assessed using random-effects Cox regression survival analyses.
One hundred thirty-seven studies were identified comprising 139 treatment arms (11 general immune stimulation, 84 vaccine, 28 antibody-based, and 16 adoptive transfer) including a total of 5,737 patients. The overall cumulative incidence of vitiligo was 3.4% (95% CI, 2.5% to 4.5%). In 27 studies reporting individual patient data, vitiligo development was significantly associated with both progression-free-survival (hazard ratio [HR], 0.51; 95% CI, 0.32 to 0.82; P < .005) and overall survival (HR, 0.25; 95% CI, 0.10 to 0.61; P < .003), indicating that these patients have two to four times less risk of disease progression and death, respectively, compared with patients without vitiligo development.
Although vitiligo occurs only in a low percentage of patients with melanoma treated with immunotherapy, our findings suggest clear survival benefit in these patients. Awareness of vitiligo induction in patients with melanoma is important as an indicator of robust antimelanoma immunity and associated improved survival.
患有黑色素瘤的患者出现白癜风样色素减退可能与更有利的临床结局相关。我们对接受免疫治疗的 III 期至 IV 期黑色素瘤患者进行了系统综述,以确定白癜风样色素减退的累积发生率以及白癜风发生对生存的预后价值。
我们系统性地检索并选择了 1995 年至 2013 年间发表的关于黑色素瘤免疫治疗中自身免疫毒性和/或白癜风的所有研究。使用适用于预后研究的系统综述的改良标准来评估每个研究的方法学质量。使用随机效应模型计算研究间白癜风样色素减退的累积发生率的综合估计值。使用随机效应 Cox 回归生存分析评估白癜风样色素减退对生存结局的预后价值。
共确定了 137 项研究,包括 139 个治疗臂(11 个全身免疫刺激,84 个疫苗,28 个抗体治疗,16 个过继转移),共纳入了 5737 例患者。白癜风的总体累积发生率为 3.4%(95%CI,2.5%至 4.5%)。在 27 项报告个体患者数据的研究中,白癜风的发生与无进展生存期(风险比[HR],0.51;95%CI,0.32 至 0.82;P<0.005)和总生存期(HR,0.25;95%CI,0.10 至 0.61;P<0.003)均显著相关,这表明与未发生白癜风的患者相比,这些患者发生疾病进展和死亡的风险分别降低了两到四倍。
尽管在接受免疫治疗的黑色素瘤患者中,白癜风的发生仅占低比例,但我们的研究结果表明这些患者的生存获益明显。在黑色素瘤患者中意识到白癜风的发生是一个强有力的抗黑色素瘤免疫和相关改善生存的指标。