Department of Internal Medicine, The University of Texas Health Science Center, Houston, TX, USA.
Department of Gastroenterology, Hepatology and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
J Cancer Res Clin Oncol. 2023 Jul;149(8):4805-4816. doi: 10.1007/s00432-022-04405-3. Epub 2022 Oct 15.
Immune checkpoint inhibitors (ICIs) are efficacious for treating various malignancies. In addition to immune-related adverse events (irAEs), growing evidence suggests that ICIs might also be associated with diverticulitis. We aim to assess the clinical presentations and management of colonic diverticulitis among cancer patients after ICI treatment.
A retrospective study was conducted on ICI-treated adult cancer patients between 01/2010 and 06/2020. Patients were grouped based on when diverticulitis developed relative to ICI treatment, either before (controls) or after (cases). Patient clinical characters, treatment, and outcomes were compared between both groups.
77 eligible patients were included: 63 patients developed diverticulitis after ICI exposure (46 had initial episode after ICI exposure, 17 had a history of diverticulitis prior then recurred after ICI exposure), and 14 had diverticulitis before ICI exposure. Diverticulitis occurred after a median of 129 days after ICI initiation. Clinical characteristics overlapped with traditional diverticulitis. 93% of patients had symptom resolution after treatment, while 23.8% experienced complications. These patients exhibited higher rates of hospitalization (87% vs 48%, P = 0.015) and surgery/interventional radiology procedures (27% vs 0, P = 0.002), and worse overall survival (P = 0.022). History of diverticulitis was not associated with a more severe disease course. Immunosuppressants (e.g., corticosteroids) were rarely required unless for concurrent ICI-mediated colitis.
Colonic diverticulitis can occur after ICI therapy at very low incidence (0.5%). Its clinical presentation, evaluation, and management are similar to traditional diverticulitis, but associated with higher complication rates requiring surgical intervention and has lower overall survival.
免疫检查点抑制剂(ICI)在治疗各种恶性肿瘤方面具有疗效。除免疫相关不良反应(irAE)外,越来越多的证据表明,ICI 还可能与憩室炎有关。我们旨在评估 ICI 治疗后癌症患者的结肠憩室炎的临床表现和治疗方法。
对 2010 年 1 月至 2020 年 6 月期间接受 ICI 治疗的成年癌症患者进行了回顾性研究。根据憩室炎相对于 ICI 治疗的发生时间将患者分组,要么在 ICI 治疗之前(对照组),要么在 ICI 治疗之后(病例组)。比较两组患者的临床特征、治疗和结局。
共纳入 77 例符合条件的患者:63 例患者在接受 ICI 暴露后发生憩室炎(46 例患者在 ICI 暴露后首次发作,17 例患者有憩室炎病史,然后在 ICI 暴露后复发),14 例患者在接受 ICI 暴露前发生憩室炎。ICI 起始后中位数 129 天后发生憩室炎。临床特征与传统憩室炎重叠。93%的患者经治疗后症状缓解,23.8%的患者出现并发症。这些患者的住院率(87% vs 48%,P=0.015)和手术/介入放射学程序发生率(27% vs 0,P=0.002)更高,总体生存率更差(P=0.022)。憩室炎病史与更严重的疾病过程无关。除非同时发生 ICI 介导的结肠炎,否则很少需要使用免疫抑制剂(如皮质类固醇)。
ICI 治疗后结肠憩室炎的发生率非常低(0.5%)。其临床表现、评估和治疗与传统憩室炎相似,但并发症发生率较高,需要手术干预,总体生存率较低。