Oral AZD5438 is a clinically translatable otoprotectant against cisplatin-induced hearing loss

Cisplatin-based chemotherapy causes hearing loss in 40-60 % of all patients, yet effective preventative options remain limited. Building on prior animal studies, we demonstrate that oral administration of AZD5438, a potent and selective CDK2 inhibitor, provides dose-dependent protection against hearing loss in a clinically relevant multi-dose cisplatin mouse model. Protective doses (4.7 and 9.4 mg/kg b.i.d.) fall within the human-equivalent maximum tolerated dose range established in AstraZeneca trials, and exhibit plasma pharmacokinetics comparable to those in humans. Importantly, AZD5438 at 9.4 mg/kg b.i.d. does not reduce cisplatin's anti-tumor efficacy in a testicular cancer xenograft model, consistent with in vitro findings. These results support AZD5438 as a promising candidate for clinical trials to prevent cisplatin-induced hearing loss while preserving cancer treatment efficacy.

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Publication Details

Journal
Neoplasia
Published
2025-11-03
DOI
https://doi.org/10.1016/j.neo.2025.101250
Primary Topic
Hearing, Cochlea, Tinnitus, Genetics
Type
article
Field-Weighted Citation Impact
0.00
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article

Oral AZD5438 is a clinically translatable otoprotectant against cisplatin-induced hearing loss

Yunlong Huang, Tal Teitz, Jian Zuo, Xianzhi Zhang et al.
Neoplasia
Hearing, Cochlea, Tinnitus, Genetics
article

Oral AZD5438 is a clinically translatable otoprotectant against cisplatin-induced hearing loss

Yunlong Huang, Tal Teitz, Jian Zuo, Xianzhi Zhang, Enrick Vesanes
article en

Abstract

Cisplatin-based chemotherapy causes hearing loss in 40-60 % of all patients, yet effective preventative options remain limited. Building on prior animal studies, we demonstrate that oral administration of AZD5438, a potent and selective CDK2 inhibitor, provides dose-dependent protection against hearing loss in a clinically relevant multi-dose cisplatin mouse model. Protective doses (4.7 and 9.4 mg/kg b.i.d.) fall within the human-equivalent maximum tolerated dose range established in AstraZeneca trials, and exhibit plasma pharmacokinetics comparable to those in humans. Importantly, AZD5438 at 9.4 mg/kg b.i.d. does not reduce cisplatin's anti-tumor efficacy in a testicular cancer xenograft model, consistent with in vitro findings. These results support AZD5438 as a promising candidate for clinical trials to prevent cisplatin-induced hearing loss while preserving cancer treatment efficacy.

NeoplasiaVol. 71
Therapeutics Clinical Research (US), Fate Therapeutics (United States) (US), Scintillon Institute (US)
Openalex Percentile: Top 68%
Hearing, Cochlea, Tinnitus, Genetics
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