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Prospective Assessment of Otologic Adverse Events due to Teprotumumab: Preliminary Results.
Kay-Rivest, Emily; Belinsky, Irina; Kozlova, Anna; Byrd, Erin; McMenomey, Sean O; Jethanamest, Daniel.
Afiliación
  • Kay-Rivest E; Department of Otolaryngology-Head & Neck Surgery, NYU Grossman School of Medicine, New York, New York, USA.
  • Belinsky I; Department of Ophthalmology, NYU Grossman School of Medicine, New York, New York, USA.
  • Kozlova A; Department of Ophthalmology, NYU Grossman School of Medicine, New York, New York, USA.
  • Byrd E; Department of Audiology, NYU Grossman School of Medicine, New York, New York, USA.
  • McMenomey SO; Department of Otolaryngology-Head & Neck Surgery, NYU Grossman School of Medicine, New York, New York, USA.
  • Jethanamest D; Department of Otolaryngology-Head & Neck Surgery, NYU Grossman School of Medicine, New York, New York, USA.
Otolaryngol Head Neck Surg ; 168(5): 1164-1169, 2023 05.
Article en En | MEDLINE | ID: mdl-36939482
OBJECTIVE: To assess a series of patients receiving teprotumumab therapy and objectively quantify the rates of otologic adverse events. STUDY DESIGN: A prospective cohort study of adult patients receiving teprotumumab between May 2020 and January 2022. SETTING: Tertiary referral center. METHODS: Prior to treatment initiation, an ototoxicity-specific audiometric battery was completed, which included conventional audiometry (frequencies 250-8000 Hz), ultrahigh-frequency audiometry (9000-20,000 Hz), tympanometry, speech discrimination scores, and distortion product otoacoustic emissions (DPOAEs). Testing was then repeated after treatment completion. RESULTS: In total, 35 patients were recruited, with a median (range) age of 48.5 years (21-74), and 8 (22.8%) were male. The most common subjective symptom reported was a hearing decline (25.7%), followed by aural fullness (17.1%) and tinnitus (14.3%). Fourteen patients had both pre- and posttreatment audiometric data. Among them, 3 patients (21.4%) were found to have changes in standard frequency audiometry, and 10 (71.4%) had changes in high-frequency audiometry, with 2 patients having changes in both. Less than half (n = 5) of the 11 patients with changes in standard or high-frequency pure tone hearing noted subjective hearing decline. Changes in DPOAE were noted in 4 patients out of 13 (30.7%). Two patients discontinued treatment due to hearing decline. Finally, 3 patients (8.6%) were diagnosed with patulous eustachian tube (PET) by an otolaryngologist, and another 3 patients are suspected to have PET based on symptom description during ophthalmologic follow-up. CONCLUSION: In our cohort, a high incidence of otologic symptoms was found to be associated with teprotumumab usage. Subjective hearing decline, changes in ultrahigh-frequency hearing as well as eustachian tube dysfunction may be encountered and suggest the potential ototoxicity of teprotumumab.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Emisiones Otoacústicas Espontáneas / Ototoxicidad Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Otolaryngol Head Neck Surg Asunto de la revista: OTORRINOLARINGOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Emisiones Otoacústicas Espontáneas / Ototoxicidad Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Otolaryngol Head Neck Surg Asunto de la revista: OTORRINOLARINGOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido