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使用伊匹木单抗继发的IgA肾病。

IgA Nephropathy Secondary to Ipilimumab Use.

作者信息

Dougherty Sean C, Desai Nisa, Cathro Helen P, Renaghan Amanda

机构信息

Department of Internal Medicine, University of Virginia, Charlottesville, Virginia, USA.

Department of Pathology, University of Virginia, Charlottesville, Virginia, USA.

出版信息

Case Rep Nephrol Dial. 2021 Nov 15;11(3):327-333. doi: 10.1159/000519169. eCollection 2021 Sep-Dec.

Abstract

Ipilimumab is a human monoclonal antibody targeting cytotoxic T-lymphocyte-associated protein 4 approved for the treatment of non-small-cell lung cancer (NSCLC) and other malignancies. Despite a high prevalence of other immune-related adverse events (irAEs), checkpoint inhibitor (CPI)-related nephrotoxicity has been reported less frequently. In this clinical case report, we describe the evaluation of a 70-year-old female with stage IV NSCLC who presented with nephrotic range proteinuria 4 weeks after receiving her first cycle of ipilimumab. She underwent a renal biopsy and was found to have IgA nephropathy that was presumed to be secondary to ipilimumab use, given recent initiation of therapy and clinical history. Unfortunately, despite prompt initiation of corticosteroids, her acute kidney injury progressed and she required hemodialysis, later transitioning to hospice. To our knowledge, this is one of few reported cases of IgA nephropathy secondary to CPI use. With increasing use of CPIs, this case further emphasizes the need for continued surveillance for irAEs, which can occur at any point in a patient's treatment course.

摘要

伊匹木单抗是一种靶向细胞毒性T淋巴细胞相关蛋白4的人源单克隆抗体,已被批准用于治疗非小细胞肺癌(NSCLC)和其他恶性肿瘤。尽管其他免疫相关不良事件(irAE)的发生率很高,但检查点抑制剂(CPI)相关的肾毒性报告较少。在本临床病例报告中,我们描述了一名70岁IV期NSCLC女性患者在接受首个周期伊匹木单抗治疗4周后出现肾病范围蛋白尿的评估情况。她接受了肾活检,鉴于近期开始治疗及临床病史,发现患有IgA肾病,推测其继发于伊匹木单抗的使用。不幸的是,尽管迅速开始使用皮质类固醇,她的急性肾损伤仍进展,需要进行血液透析,后来转为临终关怀。据我们所知,这是少数几例报告的继发于CPI使用的IgA肾病病例之一。随着CPI使用的增加,该病例进一步强调了对irAE持续监测的必要性,irAE可在患者治疗过程的任何时间发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f1/8647129/8adfa9283074/cnd-0011-0327-g01.jpg

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