Millstein Joshua, Rassekh Shahrad R, Brown Austin L, Nie Qi, Esbenshade Adam J, Knight Kristin R, Scheurer Michael E, Sung Lillian, Brooks Beth, Moke Diana J, Ross Colin J D, Wright Michael, Mena Victoria, Rushing Teresa, Carleton Bruce C, Orgel Etan
University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, CA.
Division of Pediatric Hematology/Oncology/BMT, Department of Pediatrics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
J Clin Oncol. 2025 Jul;43(19):2173-2183. doi: 10.1200/JCO-24-01861. Epub 2025 May 5.
Cisplatin treats many common tumors but causes permanent and debilitating hearing loss (HL). The objective of this study was to develop and externally validate a predictive model of HL in cisplatin-treated children and adolescent cancer survivors.
The Pediatric Holistic Evaluation of Auditory Risk (PedsHEAR) model architecture used several machine learning approaches followed by an ensemble predictor. The primary end point was post-treatment communication-affecting HL (International Society of Pediatric Oncology Ototoxicity Scale [SIOP] Grade ≥2). PedsHEAR was developed from a multicenter data set of cisplatin-exposed patients up to 21 years old (1984-2017) and externally validated using data from the Children's Oncology Group ACCL05C1 study (2007-2012) and two combined institutional cohorts (1988-2022). The model predicts post-treatment HL in each patient (probability [%], 95% CI) and classifies patients as low, intermediate, or high risk for HL (probability HL <0.33, 0.33-0.60, >0.60, respectively).
In the training data set (n = 1,115, median age 6.3 years, SIOP Grade ≥2 HL 44%), PedsHEAR demonstrated excellent discrimination (AUC, 0.93 [95% CI, 0.92 to 0.95]) and then successfully validated within the internal (testing; AUC, 0.79 [95% CI, 0.74 to 0.85]) and two external validation cohorts (AUC, 0.74 and AUC, 0.67). In an aggregate validation cohort (n = 631), the model predicted the probability of HL (AUC, 0.76 [95% CI, 0.72 to 0.79]) and classified 22% (141/631), 71% (447/631), and 7% (43/631) of patients as low, intermediate, or high risk for HL.
PedsHEAR predicted SIOP Grade ≥2 HL in pediatric cisplatin-treated patients. This is the first validated model to successfully predict cisplatin-induced HL in a broadly representative population treated with diverse regimens across a range of treatment settings.
顺铂可治疗多种常见肿瘤,但会导致永久性且使人衰弱的听力损失(HL)。本研究的目的是开发并外部验证一个针对接受顺铂治疗的儿童和青少年癌症幸存者HL的预测模型。
儿童听觉风险综合评估(PedsHEAR)模型架构采用了多种机器学习方法,随后是一个集成预测器。主要终点是治疗后影响沟通的HL(国际小儿肿瘤学会耳毒性量表[SIOP]≥2级)。PedsHEAR是根据一个多中心数据集开发的,该数据集涵盖了年龄在21岁以下(1984 - 2017年)接受顺铂治疗的患者,并使用儿童肿瘤组ACCL05C1研究(2007 - 2012年)的数据以及两个合并的机构队列(1988 - 2022年)进行外部验证。该模型预测每位患者治疗后的HL(概率[%],95%置信区间),并将患者分类为HL低、中或高风险(HL概率分别<0.33、0.33 - 0.60、>0.60)。
在训练数据集中(n = 1115,中位年龄6.3岁,SIOP≥2级HL占44%),PedsHEAR显示出出色的辨别能力(AUC,0.93 [95%置信区间,0.92至0.95]),然后在内部(测试;AUC,0.79 [95%置信区间,0.74至0.85])和两个外部验证队列(AUC,0.74和AUC,0.67)中成功得到验证。在一个汇总验证队列(n = 631)中,该模型预测了HL的概率(AUC,0.76 [95%置信区间,0.72至0.79]),并将22%(141/631)、71%(447/631)和7%(43/631)的患者分类为HL低、中或高风险。
PedsHEAR预测了接受顺铂治疗的儿科患者的SIOP≥2级HL。这是第一个在广泛代表性人群中成功预测顺铂诱导的HL的经过验证的模型,该人群接受了多种治疗方案,涉及一系列治疗环境。