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卡非佐米相关的肾毒性是常见且不可预测的:114 例多发性骨髓瘤患者的综合分析。

Carfilzomib-associated renal toxicity is common and unpredictable: a comprehensive analysis of 114 multiple myeloma patients.

机构信息

Department of Clinical Therapeutics, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Fist Department of Pathology, National and Kapodistrian University of Athens, Athens, Greece.

出版信息

Blood Cancer J. 2020 Nov 3;10(11):109. doi: 10.1038/s41408-020-00381-4.

Abstract

Carfilzomib (CFZ) is a non-reversible proteasome inhibitor approved for the treatment of patients with relapsed and refractory myeloma (RRMM). Its use has been associated with cardiovascular toxicity but although recently a signal of clinically significant renal complications has also been identified, it is less extensively investigated. We analyzed data of 114 consecutive patients with RRMM who received CFZ-based regimens. Renal complications not related to MM progression were observed in 19 (17%) patients; thrombotic microangiopathy (TMA) was seen in 6 (5%) patients, albuminuria >1 gr/day in 7 patients (6%) and at least grade 3 acute kidney injury (AKI) which could not be otherwise explained in 6 patients (5%). A total of 15 patients discontinued CFZ and dosing was reinitiated at a lower level in one patient with AKI. Albuminuria was associated with focal segmental glomerulosclerosis in the renal biopsy (performed in a total of 6 patients). Renal complications during CFZ therapy are common, occur mostly early and are unpredictable. A potential effect of CFZ on the renal endothelium could be implicated in the pathogenesis of these complications and may also share common pathophysiology with cardiovascular effects of CFZ.

摘要

卡非佐米(CFZ)是一种不可逆的蛋白酶体抑制剂,已被批准用于治疗复发和难治性多发性骨髓瘤(RRMM)患者。它的使用与心血管毒性有关,但尽管最近也发现了与临床显著肾脏并发症相关的信号,但对其研究还不够广泛。我们分析了 114 例接受 CFZ 为基础方案治疗的 RRMM 连续患者的数据。19 例(17%)患者出现与 MM 进展无关的肾脏并发症;6 例(5%)患者出现血栓性微血管病(TMA),7 例(6%)患者出现白蛋白尿>1g/天,6 例(5%)至少出现 3 级急性肾损伤(AKI),且无法用其他原因解释。共有 15 例患者停止使用 CFZ,其中 1 例 AKI 患者降低剂量重新开始治疗。在总共 6 例进行肾活检的患者中,白蛋白尿与局灶节段性肾小球硬化有关。CFZ 治疗期间的肾脏并发症很常见,大多发生在早期,且不可预测。CFZ 对肾脏内皮的潜在影响可能与这些并发症的发病机制有关,并且可能与 CFZ 的心血管作用具有共同的病理生理学机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0830/7642386/b9ece9463a65/41408_2020_381_Fig1_HTML.jpg

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