The Third Department of Internal Medicine, Faculty of Medicine, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.
Department of Diagnostic Pathology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
BMC Gastroenterol. 2020 Oct 27;20(1):355. doi: 10.1186/s12876-020-01507-5.
Diarrhea is a common adverse event of fluoropyrimidine-based chemotherapy. However, limited data are available on the frequency and risk factors of complicated chemotherapy-induced diarrhea (CID) and small intestinal mucosal damage. In this current study, we aimed to determine the incidence of complicated CID and mucosal injury among patients with complicated CID receiving fluoropyrimidine via small bowel capsule endoscopy (CE) and determined baseline risk factors associated with complicated CID.
In total, 536 patients with advanced or recurrent gastrointestinal cancer who received fluoropyrimidine-based chemotherapy were retrospectively analyzed. Diarrhea was evaluated using the Common Terminology Criteria for Adverse Events version 4. Complicated CID was defined according to the American Society of Clinical Oncology guidelines. To evaluate small intestinal mucosal injury in patients with complicated CID, CE was performed. Multivariate analysis was performed to identify risk factors for complicated CID.
Total number of 32 (6%) patients developed complicated CID. Complicating symptoms were noted in 25 (78%) patients, with cramping, vomiting, and sepsis being observed in 15 (60%), 8 (32%), and 3 (12%) patients, respectively. Among the 13 patients who underwent CE, 11 (85%) showed abnormal findings. Multivariate analysis revealed that oral fluoropyrimidine administration was a risk factor for complicated CID (odds ratio 2.95; 95% confidence interval 1.06-8.19).
Despite the relatively low incidence of complicated CID, mucosal injury of small intestine was common in patients with complicated fluoropyrimidine-induced diarrhea and oral fluoropyrimidine was an independent risk factor.
腹泻是氟嘧啶类化疗的常见不良反应。然而,关于复杂化疗引起的腹泻(CID)和小肠黏膜损伤的频率和危险因素的数据有限。在本研究中,我们旨在通过小肠胶囊内镜(CE)确定接受氟嘧啶的复杂 CID 患者中复杂 CID 的发生率和黏膜损伤,并确定与复杂 CID 相关的基线危险因素。
回顾性分析了 536 例接受氟嘧啶类化疗的晚期或复发性胃肠道癌患者。腹泻采用美国国家癌症研究所不良事件通用术语标准 4.0 版进行评估。根据美国临床肿瘤学会指南定义复杂 CID。为了评估复杂 CID 患者的小肠黏膜损伤,进行了 CE。采用多变量分析确定复杂 CID 的危险因素。
共有 32 例(6%)患者发生复杂 CID。25 例(78%)患者出现并发症症状,15 例(60%)、8 例(32%)和 3 例(12%)患者分别出现痉挛、呕吐和脓毒症。在接受 CE 的 13 例患者中,11 例(85%)显示异常。多变量分析显示,口服氟嘧啶给药是复杂 CID 的危险因素(比值比 2.95;95%置信区间 1.06-8.19)。
尽管复杂 CID 的发生率相对较低,但在有复杂氟嘧啶引起的腹泻的患者中小肠黏膜损伤很常见,并且口服氟嘧啶是一个独立的危险因素。