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Updated: Apr 30, 2026

Trans-Tympanic Drug Delivery for the Treatment of Ototoxicity
Published on: March 16, 2018
A new grading system for ototoxicity in adults
Eleonoor A R Theunissen1, Wouter A Dreschler2, Merel N Latenstein3
1Department of Head and Neck Oncology and Surgery, The Netherlands Cancer Institute, Amsterdam, The Netherlands n.theunissen@nki.nl.
A new ototoxicity grading system enhances sensitivity to hearing loss effects on speech and ultra-high sounds. This system, tested on cancer patients, proves feasible for clinical and research use.
Area of Science:
- Audiology
- Ototoxicology
- Cancer Therapeutics
Background:
- Ototoxicity, often a side effect of cancer treatments like chemotherapy and radiotherapy, can significantly impair hearing.
- Current grading systems may not fully capture the functional impact of hearing loss on daily activities.
- There is a need for a more sensitive ototoxicity assessment tool.
Purpose of the Study:
- To develop and validate a novel ototoxicity grading system.
- To enhance sensitivity to hearing deficits affecting speech intelligibility and ultra-high sound perception.
- To compare the feasibility of the new system against existing criteria (CTCAEv4, ASHA).
Main Methods:
- Incorporated pure tone averages (PTAs) for speech (1-2-4 kHz) and ultra-high frequencies (8-10-12.5 kHz).
- Considered threshold shifts and post-treatment hearing levels.
- Evaluated criteria on head and neck cancer patients undergoing (chemo-)radiotherapy ([C]RT).
Main Results:
- Grades 1 & 2 based on threshold shifts and subjective complaints.
- Grades 3 & 4 defined by specific dB hearing loss thresholds at speech-relevant frequencies.
- New criteria showed comparable results to CTCAEv4/ASHA in high-dose cisplatin cases, but higher sensitivity in RT/low-dose cisplatin scenarios.
Conclusions:
- The proposed grading system demonstrates increased sensitivity to ototoxicity compared to CTCAEv4 and ASHA.
- It offers valuable insights into how hearing loss impacts daily life functions.
- The system is deemed feasible for both clinical practice and research applications.
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