Division of Gastroenterology, Department of Internal Medicine, Iwate Medical University, Iwate, Japan.
Division of Molecular Diagnostic Pathology, Department of Pathology, School of Medicine, Iwate Medical University, Iwate, Japan.
Dig Endosc. 2020 May;32(4):616-620. doi: 10.1111/den.13555. Epub 2019 Nov 12.
We reviewed the records of patients with immune checkpoint inhibitor (ICI)-induced diarrhea during 2015 to 2019. ICI included nivolumab and ipilimumab. There were 11 patients with ICI-induced diarrhea aged 46-81 years (median, 63 years). On colonoscopy, four patients appeared normal, whereas loss of vascularity, erythema, granularity, erosions or ulcerations apparently mimicking ulcerative colitis were found in seven patients. Those seven patients had acute inflammation, cryptitis, crypt abscess and apoptosis, suggestive of ICI-induced colitis. Five of the seven patients were treated with prednisolone, two of whom were resistant to prednisolone and required infliximab. In contrast, none of the four patients without ICI-induced colitis required further treatment. Our observations suggest that diversity exists in the clinical, endoscopic and histological severity of patients with ICI-induced diarrhea. Colonoscopy together with biopsy is inevitable for the diagnosis of ICI-induced colitis, which requires intensive treatment.
我们回顾了 2015 年至 2019 年期间免疫检查点抑制剂(ICI)诱导性腹泻患者的记录。ICI 包括纳武利尤单抗和伊匹单抗。有 11 名 ICI 诱导性腹泻患者年龄在 46-81 岁之间(中位数为 63 岁)。结肠镜检查时,4 名患者表现正常,而 7 名患者出现血管丧失、红斑、颗粒状、糜烂或溃疡,明显类似于溃疡性结肠炎。这 7 名患者有急性炎症、隐窝炎、隐窝脓肿和细胞凋亡,提示为 ICI 诱导性结肠炎。7 名患者中有 5 名接受了泼尼松龙治疗,其中 2 名对泼尼松龙耐药,需要使用英夫利昔单抗。相比之下,无 ICI 诱导性结肠炎的 4 名患者无需进一步治疗。我们的观察表明,ICI 诱导性腹泻患者的临床、内镜和组织学严重程度存在差异。结肠镜检查结合活检是 ICI 诱导性结肠炎诊断所必需的,需要强化治疗。