| SENSORY ORGAN RESEARCH INSTITUTE, SEOUL NATIONAL UNIVERSITY MEDICAL RESEARCH CENTER, SEOUL, REPUBLIC OF KOREA.1 DEPARTMENT OF OTORHINOLARYNGOLOGY-HEAD AND NECK SURGERY, SEOUL NATIONAL UNIVERSITY HOSPITAL, SEOUL NATIONAL UNIVERSITY COLLEGE OF MEDICINE, SEOUL, REPUBLIC OF KOREA.2 DEPARTMENT OF OTORHINOLARYNGOLOGY-HEAD & NECK SURGERY, SAMSUNG MEDICAL CENTER, SUNGKYUNKWAN UNIVERSITY SCHOOL OF MEDICINE3 DEPARTMENT OF OTORHINOLARYNGOLOGY-HNS, SEOUL ST.MARY'S HOSPITAL, THE CATHOLIC UNIVERSITY OF KOREA4 DEPT. OF OTORHINOLARYNGOLOGY, CHUNGNAM NATIONAL UNIVERSITY SEJONG HOSPITAL5 |
¸ñÀû: Platinum-based chemotherapies, notably cisplatin and carboplatin, are
vital in treating pediatric malignancies. However, their use is
frequently associated with ototoxicity, resulting in permanent hearing
loss which can impact the quality of life of cancer survivors.
Especially for children, hearing loss affects their cognitive and
psychosocial development. This study aims to evaluate the incidence
and severity of platinum-based ototoxicity in Korean pediatric
oncology patients and to analyze potential risk factors associated
with the development of hearing loss in children with cancer. ¹æ¹ý:A retrospective cohort analysis was conducted across three major
tertiary care centers from 2004 to 2024, encompassing 377 pediatric
oncology patients treated with platinum-based regimens for a variety
of malignancies. Patients were diagnosed before the age of 19.
Audiological assessments, including pure-tone audiometry (PTA),
auditory brainstem response (ABR), and distortion product otoacoustic
emissions (DPOAE), were used to evaluate hearing thresholds before,
during, and following chemotherapy. Hearing loss was defined as a
threshold shift of 25dB or more in any frequency. Demographic data,
tumor types, chemotherapy duration, chemotherapy regimen and
additional cranial irradiation were extracted. Statistical analyses
identified significant risk factors for ototoxicity. °á°ú:In total, 212 patients met the inclusion criteria. Median age at
diagnosis was 8.2 years. 178 patients had received cisplatin, 87
received carboplatin, and 59 received both agents. Ototoxicity was
reported in 110 patients (51.9%). Among these, 90 (81.8%) had received
cisplatin, 56 (50.9%) had received carboplatin, and 38 (34.5%) had
received both agents. Notably, among the 59 patients who received both
cisplatin and carboplatin, ototoxicity was observed in 64.4%. The
incidence of ototoxicity was highest in CNS tumors, with
medulloblastoma (n=36, 32.7%) being the most prevalent, followed by
neuroblastoma (n=27, 24.5%) and sarcoma (n=22, 20%). In terms of
radiation therapy, 49 (44.5%) had received radiotherapy targeting the
head and neck region. However, the mean radiation dose did not
significantly differ between those who developed ototoxicity (40.1 Gy)
and those who did not (39.8 Gy). Additionally, ototoxicity was
significantly more prevalent in males (n=78, 70.1%) than in females
(n=32, 29.1%), with a male-to-female ratio exceeding 2:1. Moreover,
younger children appeared to be more vulnerable, as 30 patients
(45.5%) under the age of five were affected, highlighting a combined
effect of sex and age as potential risk factors. °á·Ð:This study underscores the high prevalence of platinum-induced
ototoxicity in pediatric patients, with severity influenced by tumor
type, chemotherapy regimen, and concurrent cranial irradiation. Our
findings support previous studies suggesting that male sex and younger
age, particularly under five years old, may be risk factors for
ototoxicity. Further research is warranted to validate these
associations in larger cohorts. Regular hearing evaluation is
essential for the early detection of ototoxicity. Prevention
strategies, including the use of otoprotective agents, can be
considered. Furthermore, long-term follow-up is also recommended,
particularly for patients with identified risk factors for hearing
loss. Findings emphasize the importance of routine auditory monitoring
and the potential role of otoprotective measures to preserve hearing
and improve quality of life for pediatric cancer survivors. |