Shatila Malek, Devalaraju Samanthika, Takigawa Kei, Catinis Christine, Lee Irene, Baerman Elliot, Ngo Sean, Mittal Nitish, Glombicki Stephen, Machado Antonio Pizuorno, Lu Linfeng, Aleem Abdullah Sagar, Thompson John, Funchain Pauline, Grover Shilpa, Zhang Hao Chi, Thomas Anusha Shirwaiker, Wang Yinghong
1Department of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX.
2Department of Internal Medicine, Baylor College of Medicine, Houston, TX.
J Natl Compr Canc Netw. 2025 Jun 18;23(7):e257023. doi: 10.6004/jnccn.2025.7023.
Immune checkpoint inhibitors (ICIs) for cancer carry a risk of immune-related adverse events (irAEs). Upper and lower gastrointestinal tract inflammation are common toxicities. Proton pump inhibitors (PPIs) are used to treat upper gastrointestinal irAEs. Studies have suggested these agents may also worsen lower gastrointestinal irAEs. Our study evaluated the effect of PPI exposure on gastrointestinal irAE severity.
This was a single-center retrospective chart review including all patients receiving ICIs between January 2010 and February 2024 who developed upper or lower gastrointestinal toxicity. Patients were grouped based on PPI use, defined as receiving a PPI any time from 3 months before ICI initiation until gastrointestinal toxicity diagnosis.
A total of 1,228 patients were included: 88 (7.2%) with upper gastrointestinal toxicity and 1,140 (92.8%) with lower toxicity. Upper gastrointestinal irAEs were more severe among PPI users (69.6% with grade 3 toxicity in the PPI group vs 29.6% in the non-PPI group; P<.05). Similarly, lower gastrointestinal irAEs were more severe among PPI users, with a higher need for multiple lines of biologic treatment, higher hospitalization rates, and longer hospital stays (P<.05 for all). PPI use was associated with significantly worse overall survival among patients receiving ICIs (P<.05).
Our study is the largest to date showing the impact of PPI use on immunotherapy toxicity. PPI use may predispose to more severe toxicities and worse outcomes. PPIs may also reduce immunotherapy efficacy, as reflected by worse overall survival. These findings support the judicious use of PPIs in patients receiving ICIs and call for prospective studies to validate our results.
用于癌症治疗的免疫检查点抑制剂(ICI)存在免疫相关不良事件(irAE)的风险。上、下胃肠道炎症是常见的毒性反应。质子泵抑制剂(PPI)用于治疗上胃肠道irAE。研究表明,这些药物也可能使下胃肠道irAE恶化。我们的研究评估了PPI暴露对胃肠道irAE严重程度的影响。
这是一项单中心回顾性病历审查,纳入了2010年1月至2024年2月期间接受ICI治疗并出现上或下胃肠道毒性的所有患者。根据PPI使用情况对患者进行分组,PPI使用定义为从ICI开始前3个月至胃肠道毒性诊断的任何时间接受PPI治疗。
共纳入1228例患者:88例(7.2%)出现上胃肠道毒性,1140例(92.8%)出现下胃肠道毒性。PPI使用者的上胃肠道irAE更严重(PPI组3级毒性患者占69.6%,非PPI组为29.6%;P<0.05)。同样,PPI使用者的下胃肠道irAE更严重,需要更多线生物治疗的需求更高,住院率更高,住院时间更长(所有P<0.05)。接受ICI治疗的患者中,使用PPI与总体生存率显著降低相关(P<0.05)。
我们的研究是迄今为止显示PPI使用对免疫治疗毒性影响的最大规模研究。使用PPI可能易导致更严重的毒性和更差的预后。PPI也可能降低免疫治疗疗效,总体生存率更差即反映了这一点。这些发现支持在接受ICI治疗的患者中谨慎使用PPI,并呼吁进行前瞻性研究以验证我们的结果。