Richard A Chaifetz School of Business, Saint Louis University, St. Louis, MO, United States.
School of Medicine, Saint Louis University, St. Louis, MO, United States.
JMIR Med Inform. 2024 Nov 19;12:e59480. doi: 10.2196/59480.
Prostate cancer is the second leading cause of death among American men. If detected and treated at an early stage, prostate cancer is often curable. However, an advanced stage such as metastatic castration-resistant prostate cancer (mCRPC) has a high risk of mortality. Multiple treatment options exist, the most common included docetaxel, abiraterone, and enzalutamide. Docetaxel is a cytotoxic chemotherapy, whereas abiraterone and enzalutamide are androgen receptor pathway inhibitors (ARPI). ARPIs are preferred over docetaxel due to lower toxicity. No study has used machine learning with patients' demographics, test results, and comorbidities to identify heterogeneous treatment rules that might improve the survival duration of patients with mCRPC.
This study aimed to measure patient-level heterogeneity in the association of medication prescribed with overall survival duration (in the form of follow-up days) and arrive at a set of medication prescription rules using patient demographics, test results, and comorbidities.
We excluded patients with mCRPC who were on docetaxel, cabaxitaxel, mitoxantrone, and sipuleucel-T either before or after the prescription of an ARPI. We included only the African American and white populations. In total, 2886 identified veterans treated for mCRPC who were prescribed either abiraterone or enzalutamide as the first line of treatment from 2014 to 2017, with follow-up until 2020, were analyzed. We used causal survival forests for analysis. The unit level of analysis was the patient. The primary outcome of this study was follow-up days indicating survival duration while on the first-line medication. After estimating the treatment effect, a prescription policy tree was constructed.
For 2886 veterans, enzalutamide is associated with an average of 59.94 (95% CI 35.60-84.28) more days of survival than abiraterone. The increase in overall survival duration for the 2 drugs varied across patient demographics, test results, and comorbidities. Two data-driven subgroups of patients were identified by ranking them on their augmented inverse-propensity weighted (AIPW) scores. The average AIPW scores for the 2 subgroups were 19.36 (95% CI -16.93 to 55.65) and 100.68 (95% CI 62.46-138.89). Based on visualization and t test, the AIPW score for low and high subgroups was significant (P=.003), thereby supporting heterogeneity. The analysis resulted in a set of prescription rules for the 2 ARPIs based on a few covariates available to the physicians at the time of prescription.
This study of 2886 veterans showed evidence of heterogeneity and that survival days may be improved for certain patients with mCRPC based on the medication prescribed. Findings suggest that prescription rules based on the patient characteristics, laboratory test results, and comorbidities available to the physician at the time of prescription could improve survival by providing personalized treatment decisions.
前列腺癌是美国男性死亡的第二大主要原因。如果在早期发现并治疗,前列腺癌通常是可以治愈的。然而,晚期如转移性去势抵抗性前列腺癌(mCRPC)的死亡率很高。有多种治疗选择,最常见的包括多西他赛、阿比特龙和恩扎鲁胺。多西他赛是一种细胞毒性化疗药物,而阿比特龙和恩扎鲁胺则是雄激素受体通路抑制剂(ARPI)。由于毒性较低,ARPI 优于多西他赛。没有研究使用机器学习结合患者的人口统计学、检测结果和合并症来识别可能改善 mCRPC 患者生存时间的异质治疗规则。
本研究旨在测量药物与总体生存时间(以随访天数的形式)之间关联的患者水平异质性,并根据患者的人口统计学、检测结果和合并症制定一套药物处方规则。
我们排除了在处方 ARPI 之前或之后接受多西他赛、卡巴他赛、米托蒽醌和 sipuleucel-T 治疗的 mCRPC 患者。我们仅包括非裔美国人和白人。共有 2886 名被诊断患有 mCRPC 的退伍军人在 2014 年至 2017 年期间接受了阿比特龙或恩扎鲁胺一线治疗,并进行了随访,直至 2020 年,对他们进行了分析。我们使用因果生存森林进行分析。分析的单位水平是患者。本研究的主要结局是一线药物治疗期间的随访天数,表明生存时间。在估计治疗效果后,构建了一个处方策略树。
对于 2886 名退伍军人,与阿比特龙相比,恩扎鲁胺平均可使生存时间延长 59.94(95%CI 35.60-84.28)天。两种药物的总体生存时间延长因患者的人口统计学、检测结果和合并症而异。通过对其增强逆倾向加权(AIPW)评分进行排名,确定了两组患者。两个亚组的平均 AIPW 评分为 19.36(95%CI-16.93 至 55.65)和 100.68(95%CI 62.46 至 138.89)。通过可视化和 t 检验,低和高亚组的 AIPW 评分具有统计学意义(P=.003),因此支持异质性。该分析基于医生在处方时可用的一些协变量,为两种 ARPI 制定了一套处方规则。
本研究对 2886 名退伍军人进行了研究,结果表明存在异质性,并且根据所开药物,某些 mCRPC 患者的生存时间可能会得到改善。研究结果表明,基于患者特征、实验室检测结果和医生在处方时可获得的合并症的处方规则,通过提供个性化的治疗决策,可能会改善生存。