Division of Digestive Diseases, Faculty of Medicine, Imperial College London, London, UK.
The Royal Marsden Hospital, London, UK.
Aliment Pharmacol Ther. 2020 Nov;52(9):1432-1452. doi: 10.1111/apt.15998. Epub 2020 Sep 13.
Immune checkpoint inhibitors have revolutionised cancer treatment, but at the cost of off-target immune-mediated organ damage. This includes checkpoint inhibitor-induced enterocolitis which frequently requires hospitalisation and may be life-threatening. Empiric treatment typically includes corticosteroids and infliximab, although no large-scale studies have confirmed their effectiveness.
To investigate the effectiveness of anti-inflammatory therapy in checkpoint inhibitor-induced enterocolitis METHODS: We performed a systematic review and meta-analysis of studies reporting clinical outcomes of checkpoint inhibitor-induced enterocolitis in adult cancer patients treated with anti-inflammatory agents. We searched Medline, EMBASE, and the Cochrane library through April and extracted the proportion of patients responding to anti-inflammatory therapy. Variation in effect size was studied using a random-effects meta-regression analysis, with checkpoint inhibitor agent and tumour type as the variables.
Data were pooled from 1210 treated patients across 39 studies. Corticosteroids were effective in 59% (95% CI 54- 65) of patients, with response significantly more favourable in patients treated with anti-PD-1/L1 monotherapy, compared with anti-CTLA-4 containing regimens (78%, 95% CI 69-85 vs 56 %, 95% CI 49-63, P = 0.003), and more favourable in lung cancer patients compared with melanoma patients (88%, 95% CI 62-97 vs 55%, 95% CI 47-63, P = 0.04). Infliximab was effective in 81% (95% CI 73-87) of patients, and vedolizumab in 85% (95% CI 60-96).
Corticosteroids, infliximab and vedolizumab, are effective in the treatment of checkpoint inhibitor-induced enterocolitis. Checkpoint inhibitor regimen and cancer type were significant moderators in response to corticosteroid therapy.
免疫检查点抑制剂改变了癌症治疗的格局,但也带来了靶向免疫介导的器官损伤的风险。这包括免疫检查点抑制剂诱导的肠炎,这种肠炎经常需要住院治疗,甚至可能危及生命。经验性治疗通常包括皮质类固醇和英夫利昔单抗,但没有大规模的研究证实它们的疗效。
研究抗炎治疗在免疫检查点抑制剂诱导的肠炎中的疗效。
我们对报告了接受抗炎治疗的成年癌症患者中免疫检查点抑制剂诱导的肠炎的临床结果的研究进行了系统评价和荟萃分析。我们检索了 Medline、EMBASE 和 Cochrane 图书馆,检索时间截至 4 月,并提取了接受抗炎治疗的患者对治疗有反应的比例。使用随机效应荟萃回归分析研究了效应大小的变异性,以检查点抑制剂药物和肿瘤类型为变量。
从 39 项研究中汇总了 1210 例接受治疗的患者的数据。皮质类固醇在 59%(95%CI 54-65)的患者中有效,与含有抗 CTLA-4 的方案相比,抗 PD-1/L1 单药治疗的患者反应明显更有利(78%,95%CI 69-85 与 56%,95%CI 49-63,P=0.003),且肺癌患者比黑色素瘤患者更有利(88%,95%CI 62-97 与 55%,95%CI 47-63,P=0.04)。英夫利昔单抗有效率为 81%(95%CI 73-87),vedolizumab 为 85%(95%CI 60-96)。
皮质类固醇、英夫利昔单抗和 vedolizumab 对免疫检查点抑制剂诱导的肠炎有效。检查点抑制剂方案和癌症类型是皮质类固醇治疗反应的显著调节剂。