Clinical trials evaluating transtympanic otoprotectants for cisplatin-induced ototoxicity: what do we know so far?

Sofia Waissbluth1

  • 1Department of Otolaryngology, Pontificia Universidad Católica de Chile, Santiago, Chile. sofia.waissbluth@mail.mcgill.ca.

Abstract

Insights

Transtympanic otoprotectants show promise in preventing cisplatin-induced hearing loss. Further research is needed to optimize otoprotectant choice, dosage, and timing for this chemotherapy side effect.

Area of Science:

  • Ototoxicity research
  • Chemotherapy side effect management
  • Clinical trial analysis

Background:

  • Cisplatin (CDDP) chemotherapy is associated with significant, irreversible hearing loss.
  • Systemic otoprotective strategies have yielded inconsistent results and pose interaction risks with CDDP.
  • Limited clinical trials have explored alternative otoprotection methods.

Purpose of the Study:

  • To evaluate the efficacy and challenges of transtympanic otoprotectant strategies in clinical trials.
  • To identify key variables requiring further investigation for optimal transtympanic otoprotection.
  • To synthesize findings from existing literature on this emerging therapeutic approach.

Main Methods:

  • A comprehensive literature review was conducted.
  • Focused on clinical trials investigating the transtympanic administration of otoprotectants.
  • Six relevant clinical trials were identified and analyzed.

Main Results:

  • Transtympanic delivery potentially mitigates CDDP-induced ototoxicity and avoids systemic interactions.
  • Several challenges persist, including selection of the optimal otoprotectant (e.g., sodium thiosulfate, N-acetylcysteine, dexamethasone).
  • Unresolved issues include optimal timing of injections relative to CDDP treatment, dosage, number of administrations, and associated side effects like pain and dizziness.

Conclusions:

  • The transtympanic approach presents a promising strategy for otoprotection against cisplatin-induced hearing loss.
  • Further research is essential to determine the ideal otoprotectant, its precise dosage, and the optimal injection regimen.
  • Standardization of protocols is necessary to maximize the clinical utility of this approach.