Chen Jonathan H, Pezhouh Maryam K, Lauwers Gregory Y, Masia Ricard
*Department of Pathology and Laboratory Medicine, Massachusetts General Hospital, Boston †Department of Pathology, Johns Hopkins Medical Institutions, Baltimore, MA ‡Department of Anatomic Pathology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Am J Surg Pathol. 2017 May;41(5):643-654. doi: 10.1097/PAS.0000000000000829.
Programmed cell death protein 1 (PD-1) blocking agents are novel immunotherapeutics used for treatment of advanced-stage malignancies. They have shown promise in the treatment of several malignancies, with greater efficacy and better tolerability than cytotoxic T-lymphocyte antigen 4 (CTLA-4) blocking agents. However, as with anti-CTLA-4 agents, clinically significant colitis remains an important complication. Although there is growing awareness of the histopathologic features of anti-CTLA-4 therapy, there is little information on the pathologic features of anti-PD-1 colitis. We describe here the histopathologic findings in 8 patients who developed colitis while on anti-PD-1 monotherapy. The most common pattern of injury observed (5/8 cases) was an active colitis with neutrophilic crypt microabscesses and with prominent crypt epithelial cell apoptosis and crypt atrophy/dropout. These latter features are reminiscent of other colitides with prominent apoptosis such as acute graft-versus-host disease or certain drug-induced colitides. The remainder of cases (3/8) showed a lymphocytic colitis-like pattern, characterized by increased intraepithelial lymphocytes and surface epithelial injury. Apoptosis was also often increased in these cases but crypt atrophy/dropout was not present. In patients who experienced recurrence of anti-PD-1 colitis, histologic features were similar to the initial insult but, in addition, features of chronicity developed that mimicked inflammatory bowel disease (basal lymphoplasmacytosis and crypt architectural irregularity, and Paneth cell metaplasia in 1 case). Awareness of the clinical scenario, however, should allow pathologists to suggest anti-PD-1 colitis. Interestingly, recurrent colitis was observed in patients who had been off anti-PD-1 therapy for many months. As anti-PD-1 agents are increasingly used in oncology, we present this series to increase awareness of anti-PD-1 colitis among pathologists, to facilitate its timely diagnosis and treatment.
程序性细胞死亡蛋白1(PD-1)阻断剂是用于治疗晚期恶性肿瘤的新型免疫疗法。它们在治疗多种恶性肿瘤方面已显示出前景,与细胞毒性T淋巴细胞抗原4(CTLA-4)阻断剂相比,具有更高的疗效和更好的耐受性。然而,与抗CTLA-4药物一样,临床上显著的结肠炎仍然是一个重要的并发症。尽管人们对抗CTLA-4治疗的组织病理学特征的认识不断提高,但关于抗PD-1结肠炎的病理学特征的信息却很少。我们在此描述了8例在接受抗PD-1单药治疗时发生结肠炎的患者的组织病理学发现。观察到的最常见损伤模式(5/8例)是活动性结肠炎,伴有嗜中性隐窝微脓肿,隐窝上皮细胞凋亡显著,隐窝萎缩/脱落。后一种特征让人联想到其他具有显著凋亡的结肠炎,如急性移植物抗宿主病或某些药物性结肠炎。其余病例(3/8)表现为淋巴细胞性结肠炎样模式,其特征为上皮内淋巴细胞增多和表面上皮损伤。这些病例中凋亡也常常增加,但不存在隐窝萎缩/脱落。在经历抗PD-1结肠炎复发的患者中,组织学特征与最初的损伤相似,但此外,还出现了模仿炎症性肠病的慢性特征(基底淋巴细胞浆细胞增多和隐窝结构不规则,1例出现潘氏细胞化生)。然而,了解临床情况应能使病理学家提示抗PD-1结肠炎。有趣的是,在停用抗PD-1治疗数月的患者中观察到了复发性结肠炎。随着抗PD-1药物在肿瘤学中的应用越来越广泛,我们展示本系列病例以提高病理学家对抗PD-1结肠炎的认识,促进其及时诊断和治疗。