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Updated: Nov 16, 2025

Trans-Tympanic Drug Delivery for the Treatment of Ototoxicity
Published on: March 16, 2018
Changing the time intervals between cisplatin cycles alter its ototoxic side effect.
Eric C Bielefeld1, Alicia Gonzalez1, J Riley DeBacker1
1Department of Speech and Hearing Science, The Ohio State University, 110 Pressey Hall, 1070 Carmack Road, Columbus, OH 43210, USA.
Increasing cisplatin dosing intervals reduces hearing loss and cochlear damage. Longer breaks between chemotherapy cycles minimize ototoxicity, but further research is needed to optimize timing and efficacy.
Area of Science:
- Ototoxicity research
- Cancer chemotherapy side effects
- Auditory neuroscience
Background:
- Cisplatin is a widely used chemotherapy drug.
- Ototoxicity, or hearing loss, is a common and serious side effect of cisplatin.
- Current strategies to minimize cisplatin ototoxicity include dose adjustments and early identification of hearing loss.
Purpose of the Study:
- To investigate the impact of varying inter-cycle intervals of cisplatin administration on ototoxicity.
- To determine if extending the rest periods between cisplatin cycles can reduce hearing damage.
Main Methods:
- CBA/CaJ mice received a cumulative dose of 48 mg/kg cisplatin in three cycles.
- Cycles were separated by 10, 17, or 87 days.
- Ototoxicity was assessed via auditory brainstem response threshold shifts and quantification of outer hair cell loss.
Main Results:
- Longer intervals between cisplatin cycles resulted in significantly lower auditory threshold shifts.
- Increased rest periods between doses led to reduced outer hair cell lesions in the cochlea.
- The findings suggest a dose-interval relationship in cisplatin-induced ototoxicity.
Conclusions:
- Increasing the rest intervals between cisplatin cycles is an effective strategy for reducing ototoxicity.
- Slowing down cisplatin administration by extending inter-cycle breaks can mitigate hearing loss and cochlear damage.
- Further studies are required to optimize these dosing schedules and evaluate their impact on anti-tumor efficacy.
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