Nephrotoxicity in Bispecific Antibodies Recipients: Focus on T-Cell-Engaging Bispecific Antibodies

被引:1
作者
Wen, Xiaoli [1 ]
Xu, Gaosi [1 ]
机构
[1] Nanchang Univ, Affiliated Hosp 2, Jiangxi Med Coll, Dept Nephrol, Nanchang, Jiangxi, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2024年 / 17卷
关键词
bispecific antibodies; nephrotoxicity; acute kidney injury; cytokine release syndrome; tumor lysis syndrome; cancer; PHASE-I TRIAL; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; MONOCLONAL-ANTIBODY; CATUMAXOMAB; MANAGEMENT; EFFICACY; SAFETY;
D O I
10.2147/OTT.S465679
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Recently, bispecific antibodies (BsAbs) are evolving the landscape of cancer treatment and have significantly improved the outcomes of relapsed or refractory cancer patients. As increasing BsAbs entered clinical practice, specific toxicities have emerged, and renal side-effects have been described. However, there are a lack of studies analyzing the nephrotoxicity in the anti-cancer BsAbs recipients systematically. In this review, we demonstrate the etiologies, mechanisms, other risk factors and treatment options of kidney injury in the BsAbs recipients to provide a more comprehensive insight into the nephrotoxicity post-BsAbs therapy. Significantly, due to the limited clinical trial data on each subject, we mainly conclude the related etiologies, mechanisms, and risk factors of nephrotoxicity that occur in T-cell-engaging BsAbs recipients. Nephrotoxicity associated with non-T-cell BsAbs may be associated with adverse nephrotoxicity of related monoclonal antibodies to two specific antigens. The aim of this paper is to provide nephrologists and oncologists with theoretical knowledge to provide better medical management for recipients who receive BsAbs, especially T-cellengaging BsAbs treatment.
引用
收藏
页码:545 / 556
页数:12
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