Department of Dermatology, University Hospital.
Department of Dermatology, Ambroise-Paré Hospital, APHP, Boulogne-Billancourt.
J Immunother. 2019 Jun;42(5):175-179. doi: 10.1097/CJI.0000000000000268.
Immune checkpoint inhibitors (ICI) significantly improve overall survival (OS) in patients with advanced melanoma, but immune-related colitis may occur and warrant anti-tumor necrosis factor α (TNFα) treatment in severe forms. A nationwide, multicenter retrospective survey was conducted to assess both, the real-life incidence of grade 3/4 ICI-induced colitis treated with anti-TNFα, in patients with advanced melanoma, and the consequence of this therapeutic strategy on disease outcome. All patients with advanced melanoma treated with anti-TNFα agents for severe ICI-related colitis in the participating centers were included. Relative incidence was calculated according to the total number of patients treated with ICI in network centers during the period of inclusion. The possible impact of anti-TNFα treatment on disease outcome was evaluated through comparison of objective response rate, progression-free survival, and OS with pivotal literature data. Twenty-seven patients from 13 tertiary referral centers were included. Overall, severe ICI-related colitis treated with anti-TNFα occurred in 1% of patients with advanced melanoma, mostly with ipilimumab. Infliximab was successfully used in all patients but 1, mostly after 1 infusion. OS and progression-free survival of 12 and 3 months, respectively, were observed in these patients, along with an objective response rate of 41% at 12 months. This survey shows a low real-life incidence of severe colitis requiring anti-TNFα. Response rates to immunotherapy and survival data do not appear to significantly differ from those observed in pivotal studies. Severe ICI-induced colitis requiring anti-TNFα treatment appears to be a rare event in advanced melanoma, and infliximab does not seem to adversely affect disease outcome.
免疫检查点抑制剂(ICI)显著改善了晚期黑色素瘤患者的总生存期(OS),但可能会发生免疫相关结肠炎,并需要在严重情况下使用抗肿瘤坏死因子α(TNFα)治疗。进行了一项全国性、多中心回顾性调查,以评估在晚期黑色素瘤患者中用抗 TNFα 治疗的 3/4 级 ICI 诱导结肠炎的真实发生率,以及这种治疗策略对疾病结局的影响。纳入了参与中心中用抗 TNFα 药物治疗严重 ICI 相关结肠炎的所有晚期黑色素瘤患者。相对发生率根据网络中心治疗 ICI 的患者总数计算。通过比较客观缓解率、无进展生存期和 OS 与关键文献数据,评估了抗 TNFα 治疗对疾病结局的可能影响。从 13 个三级转诊中心纳入了 27 名患者。总体而言,1%的晚期黑色素瘤患者出现严重的 ICI 相关结肠炎,且大多与伊匹单抗相关。所有患者均成功使用英夫利昔单抗,但有 1 名患者除外,主要是在第 1 次输注后。这些患者的 OS 和无进展生存期分别为 12 个月和 3 个月,12 个月时的客观缓解率为 41%。这项调查显示,需要用抗 TNFα 治疗的严重结肠炎的真实发生率较低。免疫治疗的反应率和生存数据似乎与关键研究观察到的没有显著差异。需要抗 TNFα 治疗的严重 ICI 诱导结肠炎在晚期黑色素瘤中似乎是一种罕见事件,而英夫利昔单抗似乎不会对疾病结局产生不利影响。