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Review
. 2023 May;19(5):278-283.
doi: 10.1200/OP.22.00710. Epub 2023 Mar 15.

Cisplatin-Induced Ototoxicity: A Concise Review of the Burden, Prevention, and Interception Strategies

Affiliations
Review

Cisplatin-Induced Ototoxicity: A Concise Review of the Burden, Prevention, and Interception Strategies

Asmi Chattaraj et al. JCO Oncol Pract. 2023 May.

Abstract

Cisplatin is a bedrock of cancer management and one of the most used chemotherapeutic agents in the treatment of germ cell, lung, bladder, ovarian, and head and neck cancers. Approximately 500,000 patients diagnosed annually with these cancer types in the United States could be candidates for treatment with cisplatin. There is a 5-fold increase in the risk of hearing impairment or ototoxicity with cisplatin, which can manifest as ringing in the ear (tinnitus), high-frequency hearing loss, and at late stages, a decreased ability to hear normal conversation. More than half of adult and pediatric patients with cancer treated with cisplatin developed hearing impairment with major impact on patients' health-related quality of life. A considerable evidence gap persists regarding the burden and effective prevention and interception strategies for cisplatin-induced ototoxicity, especially in adult patients with cancer. We conducted a review of the published literature to provide an update on the status of this important clinical challenge. We also surveyed practicing oncologists within our network of academic and community practices to gain a better understanding of how the published literature compares with real-world practice. Our review of the literature showed a lack of standardized guidelines for monitoring and treatment of cisplatin-induced ototoxicity, especially in the adult cancer patient population. Our survey of practicing oncologists mirrored the findings from the published literature with a heterogeneity of practice, which highlights the need for standardization.

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Conflict of interest statement

The following represents disclosure information provided by authors of this manuscript. All relationships are considered compensated unless otherwise noted. Relationships are self-held unless noted. I = Immediate Family Member, Inst = My Institution. Relationships may not relate to the subject matter of this manuscript. For more information about ASCO's conflict of interest policy, please refer to www.asco.org/rwc or ascopubs.org/op/authors/author-center.

Open Payments is a public database containing information reported by companies about payments made to US-licensed physicians (Open Payments).

Taofeek Owonikoko

Stock and Other Ownership Interests: CAMBIUM MEDICAL TECHNOLOGIES, Taobob LLC, GenCart, Coherus Biosciences

Consulting or Advisory Role: Novartis, Celgene, AbbVie, Eisai, G1 Therapeutics, Takeda, Bristol Myers Squibb, MedImmune, BerGenBio, Lilly, Amgen, AstraZeneca, PharmaMar, Boehringer Ingelheim, EMD Serono, Xcovery, Bayer, Merck, Jazz Pharmaceuticals, Zentalis, Wells Fargo, Ipsen, Eisai, Roche/Genentech, Janssen, Exelixis, BeiGene, Triptych Health Partners, Daichi, Xcovery, Coherus Biosciences

Speakers' Bureau: AbbVie

Research Funding: Novartis (Inst), Astellas Pharma (Inst), Bayer (Inst), Regeneron (Inst), AstraZeneca/MedImmune (Inst), AbbVie (Inst), G1 Therapeutics (Inst), Bristol Myers Squibb (Inst), Corvus Pharmaceuticals, United Therapeutics (Inst), Amgen (Inst), Loxo/Lilly (Inst), Fujifilm (Inst), Pfizer (Inst), Aeglea Biotherapeutics (Inst), Incyte (Inst), Merck (Inst), Oncorus (Inst), Ipsen (Inst), GlaxoSmithKline (Inst), Calithera Biosciences (Inst), Eisai (Inst), WindMIL (Inst), Turning Point Therapeutics (Inst), Roche/Genentech (Inst), Mersana (Inst), Meryx Pharmaceuticals (Inst), Boehringer Ingelheim (Inst), Boehringer Ingelheim (Inst)

Patents, Royalties, Other Intellectual Property: OVERCOMING ACQUIRED RESISTANCE TO CHEMOTHERAPY TREATMENTS THROUGH SUPPRESSION OF STAT3 (Inst), SELECTIVE CHEMOTHERAPY TREATMENTS AND DIAGNOSTIC METHODS RELATED THERETO (Inst), DR4 Modulation and its Implications in EGFR-Target Cancer Therapy Ref:18,089 PROV (CSP) United States Patent Application No. 62/670,210 June 26, 2018 (Co-Inventor) (Inst), Soluble FAS ligand as a biomarker of recurrence in thyroid cancer; provisional patent 61/727,519 (Inventor) (Inst)

Other Relationship: Roche/Genentech, EMD Serono, Novartis

Uncompensated Relationships: Reflexion Medical

Open Payments Link: https://openpaymentsdata.cms.gov/physician/253457

No other potential conflicts of interest were reported.

Figures

FIG 1.
FIG 1.
Prevalence of current ototoxicity monitoring practices by oncologists in our network (N = 35).
FIG 2.
FIG 2.
Current audiogram ordering practices by oncologists in our network (N = 35).

Comment in

References

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