{"title":"顺铂相关急性肾损伤临床预测模型的外部验证和比较:一项单中心回顾性研究","authors":"Kazuki Saito, Satoru Nihei, Junichi Asaka, Kenzo Kudo","doi":"10.1186/s40780-025-00471-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Cisplatin-associated acute kidney injury (C-AKI) is a major complication of cisplatin therapy. Although two clinical prediction models have been developed for the US population, their external validity in the Japanese population remains unclear. This study aimed to evaluate the external validity of these models and compare their predictive performances in a Japanese cohort.</p><p><strong>Methods: </strong>We assessed the performance of two C-AKI prediction models developed by Motwani et al. and Gupta et al. in a retrospective cohort of 1,684 patients treated with cisplatin at Iwate Medical University Hospital. C-AKI was defined as a ≥ 0.3 mg/dL increase in serum creatinine or a ≥ 1.5-fold rise from baseline. Severe C-AKI was defined as a ≥ 2.0-fold increase or renal replacement therapy initiation. Model performance was evaluated using discrimination (area under the receiver operating characteristic curve [AUROC]), calibration, and decision curve analysis (DCA). Logistic recalibration was applied to adapt the model to the local population.</p><p><strong>Results: </strong>The discriminatory performance for C-AKI was similar between the Gupta and Motwani models (AUROC, 0.616 vs. 0.613; p = 0.84). However, the Gupta model showed better discrimination of severe C-AKI (AUROC, 0.674 vs. 0.594; p = 0.02). Both models exhibited poor initial calibrations, which improved after recalibration. The recalibrated models yielded a greater net benefit in the DCA, with the Gupta model demonstrating the highest clinical utility in severe C-AKI.</p><p><strong>Conclusions: </strong>Both models demonstrated discriminatory ability, with the Gupta model showing particular utility in predicting severe C-AKI. Given the observed miscalibration, recalibration is essential before applying these models in Japanese clinical practice.</p>","PeriodicalId":16730,"journal":{"name":"Journal of Pharmaceutical Health Care and Sciences","volume":"11 1","pages":"82"},"PeriodicalIF":1.2000,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12482746/pdf/","citationCount":"0","resultStr":"{\"title\":\"External validation and comparison of clinical prediction models for cisplatin-associated acute kidney injury: a single-centre retrospective study.\",\"authors\":\"Kazuki Saito, Satoru Nihei, Junichi Asaka, Kenzo Kudo\",\"doi\":\"10.1186/s40780-025-00471-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Cisplatin-associated acute kidney injury (C-AKI) is a major complication of cisplatin therapy. Although two clinical prediction models have been developed for the US population, their external validity in the Japanese population remains unclear. This study aimed to evaluate the external validity of these models and compare their predictive performances in a Japanese cohort.</p><p><strong>Methods: </strong>We assessed the performance of two C-AKI prediction models developed by Motwani et al. and Gupta et al. in a retrospective cohort of 1,684 patients treated with cisplatin at Iwate Medical University Hospital. C-AKI was defined as a ≥ 0.3 mg/dL increase in serum creatinine or a ≥ 1.5-fold rise from baseline. Severe C-AKI was defined as a ≥ 2.0-fold increase or renal replacement therapy initiation. Model performance was evaluated using discrimination (area under the receiver operating characteristic curve [AUROC]), calibration, and decision curve analysis (DCA). Logistic recalibration was applied to adapt the model to the local population.</p><p><strong>Results: </strong>The discriminatory performance for C-AKI was similar between the Gupta and Motwani models (AUROC, 0.616 vs. 0.613; p = 0.84). However, the Gupta model showed better discrimination of severe C-AKI (AUROC, 0.674 vs. 0.594; p = 0.02). Both models exhibited poor initial calibrations, which improved after recalibration. The recalibrated models yielded a greater net benefit in the DCA, with the Gupta model demonstrating the highest clinical utility in severe C-AKI.</p><p><strong>Conclusions: </strong>Both models demonstrated discriminatory ability, with the Gupta model showing particular utility in predicting severe C-AKI. Given the observed miscalibration, recalibration is essential before applying these models in Japanese clinical practice.</p>\",\"PeriodicalId\":16730,\"journal\":{\"name\":\"Journal of Pharmaceutical Health Care and Sciences\",\"volume\":\"11 1\",\"pages\":\"82\"},\"PeriodicalIF\":1.2000,\"publicationDate\":\"2025-09-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12482746/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pharmaceutical Health Care and Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1186/s40780-025-00471-0\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmaceutical Health Care and Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s40780-025-00471-0","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
摘要
背景:顺铂相关性急性肾损伤(C-AKI)是顺铂治疗的主要并发症。虽然已经为美国人群开发了两种临床预测模型,但它们在日本人群中的外部有效性仍不清楚。本研究旨在评估这些模型的外部有效性,并比较它们在日本队列中的预测性能。方法:我们评估了Motwani等人和Gupta等人开发的两种C-AKI预测模型在岩手医科大学医院接受顺铂治疗的1,684例患者的回顾性队列中的性能。C-AKI定义为血清肌酐升高≥0.3 mg/dL或较基线升高≥1.5倍。重度C-AKI定义为≥2.0倍增加或开始肾脏替代治疗。使用鉴别(受试者工作特征曲线下面积[AUROC])、校准和决策曲线分析(DCA)来评估模型的性能。采用Logistic再校准使模型适应当地人口。结果:Gupta模型和Motwani模型对C-AKI的区分性能相似(AUROC, 0.616 vs. 0.613; p = 0.84)。然而,Gupta模型对严重C-AKI有更好的区分(AUROC, 0.674比0.594;p = 0.02)。两种模型都表现出较差的初始校准,重新校准后有所改善。重新校准的模型在DCA中产生了更大的净收益,Gupta模型在严重C-AKI中显示出最高的临床效用。结论:两种模型都显示出区分能力,Gupta模型在预测严重C-AKI方面显示出特别的效用。鉴于观察到的校准错误,在将这些模型应用于日本临床实践之前,重新校准是必不可少的。
External validation and comparison of clinical prediction models for cisplatin-associated acute kidney injury: a single-centre retrospective study.
Background: Cisplatin-associated acute kidney injury (C-AKI) is a major complication of cisplatin therapy. Although two clinical prediction models have been developed for the US population, their external validity in the Japanese population remains unclear. This study aimed to evaluate the external validity of these models and compare their predictive performances in a Japanese cohort.
Methods: We assessed the performance of two C-AKI prediction models developed by Motwani et al. and Gupta et al. in a retrospective cohort of 1,684 patients treated with cisplatin at Iwate Medical University Hospital. C-AKI was defined as a ≥ 0.3 mg/dL increase in serum creatinine or a ≥ 1.5-fold rise from baseline. Severe C-AKI was defined as a ≥ 2.0-fold increase or renal replacement therapy initiation. Model performance was evaluated using discrimination (area under the receiver operating characteristic curve [AUROC]), calibration, and decision curve analysis (DCA). Logistic recalibration was applied to adapt the model to the local population.
Results: The discriminatory performance for C-AKI was similar between the Gupta and Motwani models (AUROC, 0.616 vs. 0.613; p = 0.84). However, the Gupta model showed better discrimination of severe C-AKI (AUROC, 0.674 vs. 0.594; p = 0.02). Both models exhibited poor initial calibrations, which improved after recalibration. The recalibrated models yielded a greater net benefit in the DCA, with the Gupta model demonstrating the highest clinical utility in severe C-AKI.
Conclusions: Both models demonstrated discriminatory ability, with the Gupta model showing particular utility in predicting severe C-AKI. Given the observed miscalibration, recalibration is essential before applying these models in Japanese clinical practice.