肿瘤靶向治疗与免疫治疗药物致皮肤不良反应的危险因素分析及预测模型的建立

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Zimin Zhang, Mingyang Zhu, Weiwei Jiang
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引用次数: 0

摘要

肿瘤靶向治疗和免疫治疗药物比细胞毒性化疗药物具有更高的疗效和耐受性。然而,与这些新疗法相关的皮肤药物不良反应更为常见,并且仍然难以预测。迫切需要一种有效的预测模型。本回顾性研究纳入1052例患者,分为训练集、测试集和外部验证集。作为一项数据驱动的研究,共收集了76个变量。采用单因素逻辑分析、最小绝对收缩和选择算子回归、逐步逻辑回归进行特征筛选。最后,构建了9个机器学习模型并进行了比较,并进行了网格搜索来调整参数。采用标定曲线和接收机工作特性曲线下面积(AUROC)对模型性能进行评价。最终确定了9个危险因素:年龄、治疗方式、癌症类型、过敏史、年龄校正Charlson合并症指数、嗜酸性粒细胞百分比、单核细胞绝对数量、东部肿瘤合作组性能状态和c反应蛋白。其中logistic模型表现最好,在测试集(AUROC = 0.734)和外部验证集(AUROC = 0.817)上表现较好。本研究确定了9个显著的危险因素,并建立了nomogram预测模型。这些发现对于从处理皮肤药物不良反应的角度优化治疗效果和维持患者的生活质量具有重要意义。试验注册:ChiCTR2400088422。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Risk Factors Analysis of Cutaneous Adverse Drug Reactions Caused by Targeted Therapy and Immunotherapy Drugs for Oncology and Establishment of a Prediction Model

Risk Factors Analysis of Cutaneous Adverse Drug Reactions Caused by Targeted Therapy and Immunotherapy Drugs for Oncology and Establishment of a Prediction Model

Targeted therapy and immunotherapy drugs for oncology have greater efficacy and tolerability than cytotoxic chemotherapeutic drugs. However, the cutaneous adverse drug reactions associated with these newer therapies are more common and remain poorly predicted. An effective prediction model is urgently needed and essential. This retrospective study included 1052 patients, divided into train set, test set, and external validation set. As a data-driven study, a total of 76 variables were collected. Univariate logistic analysis, least absolute shrinkage and selection operator regression, and stepwise logistic regression were utilized for feature screening. Finally, nine machine-learning models were constructed and compared, and grid search was performed to adjust the parameters. Model performance was evaluated using calibration curve and the area under the receiver operating characteristic curve (AUROC). Nine risk factors were eventually identified: age, treatment modality, cancer types, history of allergies, age-corrected Charlson comorbidity index, percentage of eosinophils, absolute number of monocytes, Eastern Cooperative Oncology Group Performance Status, and C-reactive protein. Among the models, the logistic model performed best, demonstrating strong performance in test set (AUROC = 0.734) and external validation set (AUROC = 0.817). This study identified nine significant risk factors and developed a nomogram prediction model. These findings have important implications for optimizing therapeutic efficacy and maintaining the quality of life of patients from the perspective of managing cutaneous adverse drug reactions.

Trial Registration: ChiCTR2400088422

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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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