Section of Nephrology, Division of Internal Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Division of Renal Diseases and Hypertension, Department of Internal Medicine, University of Texas Health Science Center at Houston, McGovern Medical School, Houston, TX, United States.
Front Immunol. 2022 Jul 28;13:898811. doi: 10.3389/fimmu.2022.898811. eCollection 2022.
Diagnosing immune checkpoint inhibitor (ICI)-associated nephritis can be challenging since it is a rare complication of therapy, associated with a spectrum of immune-mediated pathologies, and can present months after ICI therapy discontinuation (i.e., late-onset). ICIs are increasingly administered in combination with other cancer therapies with associated nephrotoxicity, further obfuscating the diagnosis of ICI-associated nephritis. In this report, we describe the first suspected case of late-onset ICI-associated membranous nephropathy (MN) in a patient with metastatic clear cell renal cell carcinoma (RCC) who had discontinued ICI therapy 6 months prior to presentation. Prompt recognition of the suspected late-onset immune-related adverse event (irAE) resulted in the successful treatment of MN and continuation of RCC therapy.
A 57-year-old man with metastatic clear cell RCC was responsive to third-line RCC therapy with lenvatinib (oral TKI) and everolimus (oral mTOR inhibitor) when he presented with nephrotic range proteinuria and acute kidney injury (AKI). His kidney biopsy revealed probable secondary MN with subendothelial and mesangial immune complex deposits and negative staining for both phospholipase A2 receptor (PLA2R) and thrombospondin type-1 domain-containing 7A (THSD7A). While a diagnosis of paraneoplastic MN could not be excluded, the patient was responding to cancer therapy and had tumor regression. However, 6 months prior to presentation, the patient had received pembrolizumab, an ICI, with his first-line RCC treatment. Due to concern that the patient may be presenting with late-onset ICI-associated MN, he was effectively treated with rituximab, which allowed for his continued RCC therapy.
This report highlights the first case of suspected late-onset ICI-associated MN and the increasing complexity of recognizing renal irAEs. With the growing indications for the use of ICIs in combination with other cancer therapies, recognizing the various presentations of ICI-immune nephritis can help guide patient management and treatment.
诊断免疫检查点抑制剂(ICI)相关性肾炎具有挑战性,因为它是治疗的罕见并发症,与一系列免疫介导的病理有关,并且可以在 ICI 治疗停药后数月(即迟发性)出现。ICI 越来越多地与其他具有肾毒性的癌症治疗联合使用,进一步混淆了 ICI 相关性肾炎的诊断。在本报告中,我们描述了首例疑似迟发性 ICI 相关性膜性肾病(MN)的病例,患者为转移性透明细胞肾细胞癌(RCC),在出现症状前 6 个月已停止 ICI 治疗。对疑似迟发性免疫相关不良事件(irAE)的及时识别导致 MN 得到成功治疗,并继续进行 RCC 治疗。
一名 57 岁男性,患有转移性透明细胞 RCC,在接受三线 RCC 治疗(仑伐替尼[口服 TKI]和依维莫司[口服 mTOR 抑制剂])时出现肾病范围蛋白尿和急性肾损伤(AKI)。他的肾脏活检显示可能为继发性 MN,伴有内皮下和系膜免疫复合物沉积,磷脂酶 A2 受体(PLA2R)和血小板反应蛋白 1 型域包含 7A(THSD7A)均为阴性染色。虽然不能排除副肿瘤性 MN 的诊断,但患者对癌症治疗有反应且肿瘤有消退。然而,在出现症状前 6 个月,患者接受了 pembrolizumab(一种 ICI)作为一线 RCC 治疗。由于担心患者可能出现迟发性 ICI 相关性 MN,因此给予他有效的 rituximab 治疗,从而使他继续接受 RCC 治疗。
本报告强调了首例疑似迟发性 ICI 相关性 MN 的病例,以及识别肾 irAE 的日益复杂性。随着 ICI 与其他癌症治疗联合使用的适应证不断增加,识别 ICI-免疫性肾炎的各种表现有助于指导患者管理和治疗。