College of Business, Korea Advanced Institute of Science and Technology, Seoul, Republic of Korea.
Department of Urology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Clin Genitourin Cancer. 2023 Aug;21(4):e211-e218.e4. doi: 10.1016/j.clgc.2023.03.012. Epub 2023 Mar 30.
Selecting a patient-specific sequencing strategy to maximize survival outcomes is a clinically unmet need for patients with castration-resistant prostate cancer (CRPC). We developed and validated an artificial intelligence-based decision support system (DSS) to guide optimal sequencing strategy selection.
Clinicopathological data of 46 covariates were retrospectively collected from 801 patients diagnosed with CRPC at 2 high-volume institutions between February 2004 and March 2021. Cox-proportional hazards regression survival (Cox) modeling in extreme gradient boosting (XGB) was used to perform survival analysis for cancer-specific mortality (CSM) and overall mortality (OM) according to the use of abiraterone acetate, cabazitaxel, docetaxel, and enzalutamide. The models were further stratified into first-, second-, and third-line models that each provided CSM and OM estimates for each line of treatment. The performances of the XGB models were compared with those of the Cox models and random survival forest (RSF) models in terms of Harrell's C-index.
The XGB models showed greater predictive performance for CSM and OM compared to the RSF and Cox models. C-indices of 0.827, 0.807, and 0.748 were achieved for CSM in the first-, second-, and third-lines of treatment, respectively, while C-indices of 0.822, 0.813, and 0.729 were achieved for OM regarding each line of treatment, respectively. An online DSS was developed to provide visualization of individualized survival outcomes according to each line of sequencing strategy.
Our DSS can be used in clinical practice by physicians and patients as a visualized tool to guide the sequencing strategy of CRPC agents.
为了最大程度地提高生存结果,选择针对特定患者的测序策略是去势抵抗性前列腺癌(CRPC)患者尚未满足的临床需求。我们开发并验证了一种基于人工智能的决策支持系统(DSS),以指导最佳测序策略选择。
回顾性收集了 2004 年 2 月至 2021 年 3 月期间在 2 家高容量机构被诊断为 CRPC 的 801 名患者的 46 个协变量的临床病理数据。使用极端梯度增强(XGB)的 Cox 比例风险生存(Cox)模型对醋酸阿比特龙、卡巴他赛、多西他赛和恩扎鲁胺的使用进行生存分析,以评估癌症特异性死亡率(CSM)和总死亡率(OM)。这些模型进一步分为一线、二线和三线模型,每个模型均为每条治疗线提供 CSM 和 OM 估计值。根据 Harrell's C 指数比较了 XGB 模型与 Cox 模型和随机生存森林(RSF)模型的性能。
与 RSF 和 Cox 模型相比,XGB 模型对 CSM 和 OM 的预测性能更高。在一线、二线和三线治疗中,CSM 的 C 指数分别为 0.827、0.807 和 0.748,而在每条治疗线中,OM 的 C 指数分别为 0.822、0.813 和 0.729。开发了一个在线 DSS,根据每个测序策略提供个体化生存结果的可视化。
我们的 DSS 可由医生和患者在临床实践中用作指导 CRPC 药物测序策略的可视化工具。