Department of Pathology, Clinica Universidad de Navarra (CUN), Pamplona, Spain.
Department of Oncology, Clinica Universidad de Navarra (CUN), Pamplona, Spain.
Oncoimmunology. 2020 May 13;9(1):1760676. doi: 10.1080/2162402X.2020.1760676.
Checkpoint inhibitors have improved the survival of patients with advanced tumors and show a manageable toxicity profile. However, auto-immune colitis remains a relevant side effect, and combinations of anti-PD1/PDL1 and anti-CTLA-4 increase its incidence and severity. Here, we report the case of a 50-year-old patient diagnosed with stage IV cervical cancer that relapsed following radical surgery, external radiation/brachytherapy and standard chemotherapy. She was subsequently treated with Nivolumab and Ipilimumab combination and developed grade 2 colitis presenting a dissociation between endoscopic and pathological findings. At cycle 10 the patient reported grade 3 diarrhea and abdominal discomfort, without blood or mucus in the stools. Immunotherapy was withheld and a colonoscopy was performed, showing normal mucosa in the entire colon. Puzzlingly, histologic evaluation of randomly sampled mucosal biopsy of the distal colon showed an intense intraepithelial lymphocyte infiltration with crypt loss and some regenerating crypts with a few apoptotic bodies set in a chronically inflamed lamina propria, consistent with the microscopic diagnosis of colitis. Treatment with methylprednisolone 2 mg/kg was initiated which led to a decrease in the number of stools to grade 1. Additional investigations to exclude other causes of diarrhea rendered negative results. The patient experienced a major partial response and, following the resolution of diarrhea, she was re-challenged again with immunotherapy, with the reappearance of grade 2 diarrhea, leading to permanent immunotherapy interruption. We conclude and propose that performing random colonic biopsies should be considered in cases of immune checkpoint-associated unexplained diarrhea, even when colonoscopy shows macroscopically normal colonic mucosa inflammatory lesions.
检查点抑制剂提高了晚期肿瘤患者的生存率,并表现出可管理的毒性特征。然而,自身免疫性结肠炎仍然是一个相关的副作用,抗 PD1/PDL1 和抗 CTLA-4 的联合使用增加了其发生率和严重程度。在这里,我们报告了一例 50 岁的患者,该患者被诊断为 IV 期宫颈癌,根治性手术后复发,接受了外部放射治疗/近距离放射治疗和标准化疗。随后,她接受了 Nivolumab 和 Ipilimumab 的联合治疗,并出现了 2 级结肠炎,表现为内镜和病理检查结果不一致。在第 10 个周期时,患者报告出现 3 级腹泻和腹部不适,粪便中没有血液或粘液。免疫治疗被暂停,并进行了结肠镜检查,整个结肠的黏膜均正常。令人费解的是,远端结肠随机取样黏膜活检的组织学评估显示,上皮内淋巴细胞浸润强烈,伴有隐窝丢失,一些再生隐窝中可见少量凋亡小体,固有层呈慢性炎症,符合结肠炎的微观诊断。开始使用 2mg/kg 的甲基强的松龙进行治疗,这导致粪便次数减少至 1 级。进一步排除其他腹泻原因的检查结果均为阴性。患者经历了主要的部分缓解,腹泻缓解后,再次重新接受免疫治疗,出现 2 级腹泻,导致免疫治疗永久中断。我们得出结论并提出,即使结肠镜检查显示宏观上正常的结肠黏膜炎症病变,对于免疫检查点相关的不明原因腹泻,应考虑进行随机结肠活检。