Cai Lie, Deutsch Thomas M, Sidey-Gibbons Chris, Kobel Michelle, Riedel Fabian, Smetanay Katharina, Fremd Carlo, Michel Laura, Golatta Michael, Heil Joerg, Schneeweiss Andreas, Pfob André
Department of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
MD Anderson Center for INSPiRED Cancer Care (Integrated Systems for Patient-Reported Data), The University of Texas MD Anderson Cancer Center, Houston, TX.
JCO Clin Cancer Inform. 2024 Dec;8:e2400010. doi: 10.1200/CCI.24.00010. Epub 2024 Dec 23.
Toxicity to systemic cancer treatment represents a major anxiety for patients and a challenge to treatment plans. We aimed to develop machine learning algorithms for the upfront prediction of an individual's risk of experiencing treatment-relevant toxicity during the course of treatment.
Clinical records were retrieved from a single-center, consecutive cohort of patients who underwent neoadjuvant treatment for early breast cancer. We developed and validated machine learning algorithms to predict grade 3 or 4 toxicity (anemia, neutropenia, deviation of liver enzymes, nephrotoxicity, thrombopenia, electrolyte disturbance, or neuropathy). We used 10-fold cross-validation to develop two algorithms (logistic regression with elastic net penalty [GLM] and support vector machines [SVMs]). Algorithm predictions were compared with documented toxicity events and diagnostic performance was evaluated via area under the curve (AUROC).
A total of 590 patients were identified, 432 in the development set and 158 in the validation set. The median age was 51 years, and 55.8% (329 of 590) experienced grade 3 or 4 toxicity. The performance improved significantly when adding referenced treatment information (referenced regimen, referenced summation dose intensity product) in addition to patient and tumor variables: GLM AUROC 0.59 versus 0.75, = .02; SVM AUROC 0.64 versus 0.75, = .01.
The individual risk of treatment-relevant toxicity can be predicted using machine learning algorithms. We demonstrate a promising way to improve efficacy and facilitate proactive toxicity management of systemic cancer treatment.
全身癌症治疗的毒性是患者的主要担忧,也是治疗计划面临的挑战。我们旨在开发机器学习算法,用于在治疗过程中预先预测个体发生与治疗相关毒性的风险。
从一个单中心连续队列中检索接受早期乳腺癌新辅助治疗患者的临床记录。我们开发并验证了机器学习算法以预测3级或4级毒性(贫血、中性粒细胞减少、肝酶偏差、肾毒性、血小板减少、电解质紊乱或神经病变)。我们使用10折交叉验证来开发两种算法(带弹性网罚项的逻辑回归[GLM]和支持向量机[SVM])。将算法预测结果与记录的毒性事件进行比较,并通过曲线下面积(AUROC)评估诊断性能。
共纳入590例患者,其中432例在开发集,158例在验证集。中位年龄为51岁,55.8%(590例中的329例)发生3级或4级毒性。除患者和肿瘤变量外,加入参考治疗信息(参考方案、参考总剂量强度乘积)时性能显著提高:GLM的AUROC从0.59提高到0.75,P = 0.02;SVM的AUROC从0.64提高到0.75,P = 0.01。
可使用机器学习算法预测与治疗相关毒性的个体风险。我们展示了一种有望提高全身癌症治疗疗效并促进主动毒性管理的方法。