{"title":"Case report: A case of pseudo-acute kidney injury due to cyclin-dependent kinase inhibitor","authors":"P. Errabelli, Maulik K Lathiya, Devender Singh","doi":"10.3389/fneph.2024.1389562","DOIUrl":null,"url":null,"abstract":"Various classes of targeted therapies have emerged in the last few years, which have revolutionized cancer treatment, and improved the prognosis and survival of cancer patients. Unfortunately, these agents have serious toxic effects on the kidneys. Some of the toxic effects are hypertension, acute kidney injury (AKI), and proteinuria. One interesting phenomenon that has emerged recently is pseudo-acute kidney injury due to the interference with the tubular secretion of creatinine by some of the targeted therapeutic agents. Understanding this physiology is needed to avoid unnecessary investigation and withholding of lifesaving chemo regimen. Alternative methods to assess renal function such as cystatin C-based estimated glomerular filtration rate (eGFR) can differentiate true AKI from pseudo-AKI. Here, we describe one such case of pseudo-AKI from cyclin-dependent kinase (CDK) 4/6 inhibitor, abemaciclib, which inhibits tubular secretion of creatinine. Using cystatin-C-based eGFR revealed pseudo-AKI in this case.","PeriodicalId":502454,"journal":{"name":"Frontiers in Nephrology","volume":" 44","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Nephrology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fneph.2024.1389562","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Various classes of targeted therapies have emerged in the last few years, which have revolutionized cancer treatment, and improved the prognosis and survival of cancer patients. Unfortunately, these agents have serious toxic effects on the kidneys. Some of the toxic effects are hypertension, acute kidney injury (AKI), and proteinuria. One interesting phenomenon that has emerged recently is pseudo-acute kidney injury due to the interference with the tubular secretion of creatinine by some of the targeted therapeutic agents. Understanding this physiology is needed to avoid unnecessary investigation and withholding of lifesaving chemo regimen. Alternative methods to assess renal function such as cystatin C-based estimated glomerular filtration rate (eGFR) can differentiate true AKI from pseudo-AKI. Here, we describe one such case of pseudo-AKI from cyclin-dependent kinase (CDK) 4/6 inhibitor, abemaciclib, which inhibits tubular secretion of creatinine. Using cystatin-C-based eGFR revealed pseudo-AKI in this case.
过去几年中出现的各类靶向疗法给癌症治疗带来了革命性的变化,改善了癌症患者的预后和存活率。遗憾的是,这些药物对肾脏有严重的毒性作用。其中一些毒副作用包括高血压、急性肾损伤(AKI)和蛋白尿。最近出现的一个有趣现象是假性急性肾损伤,这是由于一些靶向治疗药物干扰了肾小管分泌肌酐。需要了解这一生理现象,以避免不必要的检查和暂停挽救生命的化疗方案。评估肾功能的其他方法,如基于胱抑素 C 的估计肾小球滤过率(eGFR),可以区分真正的 AKI 和假性 AKI。在这里,我们描述了一例由细胞周期蛋白依赖性激酶(CDK)4/6抑制剂阿柏西尼(abemaciclib)引起的假性AKI,阿柏西尼会抑制肾小管分泌肌酐。使用基于胱抑素 C 的 eGFR 发现该病例为假性 AKI。