Leiden University Medical Center, Leiden, the Netherlands (M.K.V., O.M.D., E.K.).
University Medical Center Utrecht, Utrecht, the Netherlands (K.P.S.).
Ann Intern Med. 2021 May;174(5):641-648. doi: 10.7326/M20-3419. Epub 2021 Feb 16.
Because immune checkpoint inhibition (ICI) can cause immune-related adverse events (irAEs) mimicking immunologic diseases, patients with preexisting autoimmune disease (AID) have been excluded from clinical trials.
To evaluate the safety and efficacy of ICI in patients with advanced melanoma with and without AID.
Nationwide cohort study.
The Netherlands.
4367 patients with advanced melanoma enrolled in the Dutch Melanoma Treatment Registry (DMTR) between July 2013 and July 2018 and followed through February 2019.
Patient, clinical, and treatment characteristics; irAEs of grade 3 or higher; treatment response; and survival.
A total of 415 patients (9.5%) had AID, categorized as rheumatologic AID ( = 227), endocrine AID ( = 143), inflammatory bowel disease (IBD) ( = 55), or "other" ( = 8). Of these, 228 patients (55%) were treated with ICI (vs. 2546 [58%] without AID); 87 were treated with anti-cytotoxic T lymphocyte-associated protein 4 (CTLA-4), 187 with anti-programmed cell death 1 (PD-1), and 34 with the combination. The incidences of irAEs of grade 3 or higher in patients with AID were 30% (95% CI, 21% to 41%) with anti-CTLA-4, 17% (CI, 12% to 23%) with anti-PD-1, and 44% (CI, 27% to 62%) with combination therapy; for patients without AID, the incidences were 30% (CI, 27% to 33%) ( = 916), 13% (CI, 12% to 15%) ( = 1540), and 48% (CI, 43% to 53%) ( = 388), respectively. Patients with AID more often discontinued anti-PD-1 treatment because of toxicity than patients without AID (17% [CI, 12% to 23%] vs. 9% [CI, 8% to 11%]). Patients with IBD were more prone to anti-PD-1-induced colitis (6/31 = 19% [CI, 7% to 37%]) than patients with other AIDs (3% [CI, 0% to 6%]) and patients without AID (2% [CI, 2% to 3%]).The objective response rate was similar in patients with versus without AID who were treated with anti-CTLA-4 (10% [CI, 5% to 19%] vs. 16% [CI, 14% to 19%]), anti-PD-1 (40% [CI, 33% to 47%] vs. 44% [CI, 41% to 46%]), or the combination (39% [CI, 20% to 59%] vs. 43% [CI, 38% to 49%]). Survival did not differ between patients with and those without AID (median, 13 months [CI, 10 to 16 months] vs. 14 months [CI, 13 to 15 months]).
Information was limited on AID severity and immunosuppressive treatment.
Response to ICI with anti-CTLA-4, anti-PD-1, or their combination for advanced melanoma and overall incidence of any irAEs of grade 3 or higher were similar in patients with and without preexisting AID. However, severe colitis and toxicity requiring early discontinuation of treatment occurred more frequently among patients with preexisting IBD, warranting close follow-up.
The Netherlands Organization for Health Research and Development.
由于免疫检查点抑制(ICI)可能会引起类似于免疫性疾病的免疫相关不良反应(irAEs),因此患有自身免疫性疾病(AID)的患者已被排除在临床试验之外。
评估有和没有 AID 的晚期黑色素瘤患者接受 ICI 治疗的安全性和疗效。
全国性队列研究。
荷兰。
2013 年 7 月至 2018 年 7 月期间在荷兰黑色素瘤治疗登记处(DMTR)登记的 4367 名晚期黑色素瘤患者,并随访至 2019 年 2 月。
患者、临床和治疗特征;3 级或更高级别的 irAEs;治疗反应;和生存。
共有 415 名(9.5%)患者患有 AID,分为风湿性 AID(=227)、内分泌 AID(=143)、炎症性肠病(IBD)(=55)或“其他”(=8)。其中,228 名(55%)患者接受 ICI 治疗(vs. 无 AID 的 2546 名[58%]);87 名接受抗细胞毒性 T 淋巴细胞相关蛋白 4(CTLA-4)治疗,187 名接受抗程序性细胞死亡 1(PD-1)治疗,34 名接受联合治疗。AID 患者发生 3 级或更高级别的 irAEs 的发生率为 30%(95%CI,21%至 41%)与抗 CTLA-4,17%(CI,12%至 23%)与抗 PD-1,和 44%(CI,27%至 62%)与联合治疗;对于无 AID 的患者,发生率分别为 30%(CI,27%至 33%)(=916)、13%(CI,12%至 15%)(=1540)和 48%(CI,43%至 53%)(=388)。与无 AID 的患者相比,AID 患者因毒性而更频繁地停止抗 PD-1 治疗(17%[CI,12%至 23%]与 9%[CI,8%至 11%])。患有 IBD 的患者比患有其他 AID(6/31=19%[CI,7%至 37%])和无 AID 的患者(2%[CI,2%至 3%])更容易发生抗 PD-1 诱导的结肠炎。接受抗 CTLA-4、抗 PD-1 或联合治疗的 AID 患者与无 AID 患者的客观缓解率相似(抗 CTLA-4:10%[CI,5%至 19%]与 16%[CI,14%至 19%];抗 PD-1:40%[CI,33%至 47%]与 44%[CI,41%至 46%];联合治疗:39%[CI,20%至 59%]与 43%[CI,38%至 49%])。有和没有 AID 的患者的生存没有差异(中位生存时间,13 个月[CI,10 至 16 个月]与 14 个月[CI,13 至 15 个月])。
关于 AID 严重程度和免疫抑制治疗的信息有限。
在晚期黑色素瘤患者中,接受抗 CTLA-4、抗 PD-1 或联合治疗的反应率以及任何 3 级或更高级别的 irAEs 的总发生率在有和没有预先存在 AID 的患者中相似。然而,预先存在的 IBD 患者更常发生严重结肠炎和需要早期停止治疗的毒性,需要密切随访。
荷兰健康研究与发展组织。