Department of Pediatric Oncology, Princess Maxima Center for Pediatric Oncology, Utrecht, the Netherlands.
British Columbia Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
Cancer. 2022 Jan 1;128(1):169-179. doi: 10.1002/cncr.33848. Epub 2021 Sep 7.
Ototoxicity is a common adverse event of cisplatin treatment. The authors investigated the development of cisplatin-induced hearing loss (CIHL) over time in children with cancer by age and examined the influence of other clinical characteristics on the course of CIHL.
Data from Canadian patients with childhood cancer were retrospectively reviewed. Hearing loss was graded according to International Society of Pediatric Oncology criteria. The Kaplan-Meier method was applied to estimate the cumulative incidence of CIHL for the total cohort and according to age. Cox regression models were used to explore the effects of independent variables on CIHL development up to 3 years after the start of therapy.
In total, 368 patients with 2052 audiological assessments were included. Three years after initiating therapy, the cumulative incidence of CIHL was highest in patients aged ≤5 years (75%; 95% confidence interval [CI], 66%-84%), with a rapid increase observed to 27% (95% CI, 21%-35%) at 3 months and to 61% (95% CI, 53%-69%) at 1 year, compared with patients aged >5 years (48%; 95% CI, 37%-62%; P < .001). The total cumulative dose of cisplatin at 3 months (per 100 mg/m increase: hazard ratio [HR], 1.20; 95% CI, 1.01-1.41) vincristine (HR, 2.87; 95% CI, 1.89-4.36) and the total duration of concomitantly administered antibiotics (>30 days: HR, 1.85; 95% CI, 1.17-2.95) further influenced CIHL development over time.
In young children, the cumulative incidence of CIHL is higher compared with that in older children and develops early during therapy. The course of CIHL is further influenced by the total cumulative dose of cisplatin and other ototoxic (co-)medication. These results highlight the need for audiological monitoring at each cisplatin cycle.
耳毒性是顺铂治疗的常见不良反应。作者通过年龄研究了癌症患儿顺铂诱导听力损失(CIHL)随时间的发展,并检查了其他临床特征对 CIHL 进程的影响。
回顾性分析加拿大儿童癌症患者的数据。根据国际儿科肿瘤学会标准对听力损失进行分级。应用 Kaplan-Meier 法估计总队列和按年龄分层的 CIHL 累积发生率。Cox 回归模型用于探索独立变量对治疗开始后 3 年内 CIHL 发展的影响。
共纳入 368 例患者,共进行了 2052 次听力评估。治疗开始后 3 年,≤5 岁患者的 CIHL 累积发生率最高(75%;95%置信区间 [CI],66%-84%),在 3 个月时迅速增加至 27%(95% CI,21%-35%),在 1 年时增加至 61%(95% CI,53%-69%),而>5 岁患者的 CIHL 累积发生率为 48%(95% CI,37%-62%;P <.001)。3 个月时顺铂总累积剂量(每增加 100mg/m:风险比 [HR],1.20;95% CI,1.01-1.41)、长春新碱(HR,2.87;95% CI,1.89-4.36)和同时使用抗生素的总持续时间(>30 天:HR,1.85;95% CI,1.17-2.95)进一步影响 CIHL 随时间的发展。
在幼儿中,CIHL 的累积发生率高于年长儿童,且在治疗早期即发展。CIHL 的进程还受到顺铂总累积剂量和其他耳毒性(联合)药物的影响。这些结果强调了在每个顺铂周期都需要进行听力监测。