耳蜗剂量和放疗年龄可预测髓母细胞瘤患儿接受被动散射质子疗法和顺铂治疗后的严重听力损失。

IF 16.4 1区 医学 Q1 CLINICAL NEUROLOGY Neuro-oncology Pub Date : 2024-10-03 DOI:10.1093/neuonc/noae114
Mohammad H Abu-Arja, Austin L Brown, Jack M Su, M Fatih Okcu, Holly B Lindsay, Susan L McGovern, Mary Frances McAleer, David R Grosshans, Murali M Chintagumpala, Arnold C Paulino
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It was 8.9% (95% CI: 2.3-31.6) and 15.6% (95% CI: 5.3-41.1) for children with Dmc <36 Gy and age at radiotherapy ≥7 and <7 years, respectively (P = .78).</p><p><strong>Conclusions: </strong>Children <7 years at radiotherapy with a Dmc ≥36 Gy are at higher risk for HL.</p>","PeriodicalId":19377,"journal":{"name":"Neuro-oncology","volume":" ","pages":"1912-1920"},"PeriodicalIF":16.4000,"publicationDate":"2024-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11449093/pdf/","citationCount":"0","resultStr":"{\"title\":\"The cochlear dose and the age at radiotherapy predict severe hearing loss after passive scattering proton therapy and cisplatin in children with medulloblastoma.\",\"authors\":\"Mohammad H Abu-Arja, Austin L Brown, Jack M Su, M Fatih Okcu, Holly B Lindsay, Susan L McGovern, Mary Frances McAleer, David R Grosshans, Murali M Chintagumpala, Arnold C Paulino\",\"doi\":\"10.1093/neuonc/noae114\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Hearing loss (HL) is associated with worse neurocognitive outcomes among patients with medulloblastoma. 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引用次数: 0

摘要

背景:听力损失(HL)与髓母细胞瘤患者较差的神经认知结果有关。我们旨在确定与严重听力损失相关的风险因素,并评估已发表的听力损失计算器在接受被动散射质子疗法(PSPT)和顺铂治疗的患者中的通用性:我们确定了2007-2022年间在本中心接受治疗的3-21岁患者。采用国际儿科肿瘤学会波士顿分级法对听力图进行分级。使用 Kaplan-Meier 模型和多变量 Cox 模型评估 3-4 级 HL 的发生时间,以估计危险比 (HR) 和 95% 置信区间 (CI):79名患者接受了PSPT治疗,中位年龄为7.5岁(3.1-21.1岁)。平均耳蜗剂量(Dmc)(±S.D.)为 31.5±8.5 Gy,累计顺铂剂量为 295±50 mg/m2。59名患者(75%)接受了阿米福星治疗。患者完成的听力检查中位数为 9 次(范围:4-22),听力检查随访中位数为 49 个月(范围:6-177)。27名患者(34%)患有3-4级HL。在调整后的 Cox 模型中,只有较高的 Dmc(HR=1.12,95% CI:1.06-1.18)与 3-4 级 HL 相关。预测3-4级HL的3年发生率为40.0%(95% CI:21.3-66.3),Dmc≥36 Gy且放疗时年龄≥7岁的儿童为66.7%(95% CI:35.4-93.7):儿童
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The cochlear dose and the age at radiotherapy predict severe hearing loss after passive scattering proton therapy and cisplatin in children with medulloblastoma.

Background: Hearing loss (HL) is associated with worse neurocognitive outcomes among patients with medulloblastoma. We aimed to identify risk factors associated with severe HL and to evaluate the generalizability of a published HL calculator among patients treated with passive scattering proton therapy (PSPT) and cisplatin.

Methods: We identified patients aged 3-21 years who were treated at our centers between 2007 and 2022. Audiograms were graded using the International Society of Pediatric Oncology (SIOP) Boston scale. Time to grades 3-4 HL was evaluated using Kaplan-Meier and multivariable Cox models to estimate hazard ratios and 95% confidence intervals (CI).

Results: Seventy-nine patients were treated with PSPT at a median age of 7.5 years (range: 3.1-21.1). The mean cochlear dose (Dmc) (±SD) was 31.5 ± 8.5 Gy, and the cumulative cisplatin dose was 295 ± 50 mg/m2. Fifty-nine patients (75%) received amifostine. Patients completed a median of 9 audiograms (range: 4-22) with a median audiogram follow-up of 49 months (range: 6-177). Twenty-seven patients (34%) had grades 3-4 HL. In adjusted Cox models, only higher Dmc (HR = 1.12, 95% CI:1.06-1.18) was associated with grades 3-4 HL. The predicted 3-year incidence of grades 3-4 HL was 40.0% (95% CI: 21.3-66.3) and 66.7% (95% CI: 35.4-93.7) for children with Dmc ≥36 Gy and age at radiotherapy ≥7 and <7 years, respectively (P = .042). It was 8.9% (95% CI: 2.3-31.6) and 15.6% (95% CI: 5.3-41.1) for children with Dmc <36 Gy and age at radiotherapy ≥7 and <7 years, respectively (P = .78).

Conclusions: Children <7 years at radiotherapy with a Dmc ≥36 Gy are at higher risk for HL.

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来源期刊
Neuro-oncology
Neuro-oncology 医学-临床神经学
CiteScore
27.20
自引率
6.30%
发文量
1434
审稿时长
3-8 weeks
期刊介绍: Neuro-Oncology, the official journal of the Society for Neuro-Oncology, has been published monthly since January 2010. Affiliated with the Japan Society for Neuro-Oncology and the European Association of Neuro-Oncology, it is a global leader in the field. The journal is committed to swiftly disseminating high-quality information across all areas of neuro-oncology. It features peer-reviewed articles, reviews, symposia on various topics, abstracts from annual meetings, and updates from neuro-oncology societies worldwide.
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