Department of Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 1N4, Canada.
Medical Affairs, Bayer Inc., Mississauga, ON L4W 5R6, Canada.
Curr Oncol. 2023 Sep 1;30(9):8149-8158. doi: 10.3390/curroncol30090591.
Over the past decade, the treatment of metastatic castration-sensitive prostate cancer (mCSPC) has changed significantly. Current guidelines suggest the use of androgen deprivation therapy (ADT) plus an additional systemic therapy, regardless of disease burden and risk, based on phase 1 evidence showing improved overall survival. We sought to describe treatment patterns of patients with mCSPC in the province of Alberta.
This was a retrospective, population-based, cohort study of male patients aged ≥18 with mCSPC at the time of diagnosis and who initiated ADT between 1 January 2016 and 31 December 2020. Data were obtained from the Alberta Cancer Registry. Patients were assigned to an ADT-alone cohort or a treatment intensification cohort (cohorts 2-5). The primary objectives of this study were to describe baseline characteristics and the treatment of mCSPC patients who initiated ADT with or without treatment intensification. Overall survival between cohorts was a secondary objective. Descriptive statistics were used to describe differences in baseline characteristics of each cohort. Overall survival was calculated using the Kaplan-Meier method. All statistical tests were two-sided and are used to call out likely cohort differences descriptively.
Between 1 January 2016 and 31 December 2020, we identified a total of 960 patients with mCSPC (median age 74 years, IQR 66-82). Most patients received ADT alone (67%), followed by ADT plus abiraterone (18%), ADT plus docetaxel (12%), and ADT plus enzalutamide or apalutamide (3%). Over the study period, we observed an increase in the utilization of treatment intensification over time, in particular, the increased use of androgen-receptor-axis-targeted (ARAT) therapies. Patients who received ADT alone were older, were more likely to have more than one comorbid condition, had fewer sites of metastatic disease, and were less likely to be on opioid medications.
In this study, we show that patients who received ADT alone as treatment for mCSPC are older, have more comorbidities, and have less extensive disease. While there has been a decline over time in the number of patients treated with ADT alone, over 50% of all patients with mCSPC continue to receive ADT alone. Further work is needed to understand barriers to treatment intensification and for knowledge translation initiatives to improve the treatment of patients with mCSPC.
在过去的十年中,转移性去势敏感型前列腺癌(mCSPC)的治疗发生了重大变化。目前的指南建议根据显示总生存期改善的 1 期证据,无论疾病负担和风险如何,均使用雄激素剥夺疗法(ADT)加额外的全身治疗。我们旨在描述艾伯塔省 mCSPC 患者的治疗模式。
这是一项回顾性、基于人群的队列研究,纳入了 2016 年 1 月 1 日至 2020 年 12 月 31 日诊断时患有 mCSPC 且开始 ADT 的年龄≥18 岁的男性患者。数据来自艾伯塔癌症登记处。患者被分配到 ADT 单药治疗组或治疗强化组(队列 2-5)。本研究的主要目的是描述开始 ADT 治疗且未强化治疗或强化治疗的 mCSPC 患者的基线特征和治疗情况。各组之间的总生存期为次要目标。使用描述性统计来描述每个队列的基线特征差异。使用 Kaplan-Meier 法计算总生存期。所有统计检验均为双侧检验,用于描述性地指出可能的队列差异。
2016 年 1 月 1 日至 2020 年 12 月 31 日期间,共确定了 960 名患有 mCSPC 的患者(中位年龄 74 岁,IQR 66-82)。大多数患者接受 ADT 单药治疗(67%),其次是 ADT 联合阿比特龙(18%)、ADT 联合多西他赛(12%)和 ADT 联合恩杂鲁胺或阿帕鲁胺(3%)。在研究期间,我们观察到随着时间的推移,治疗强化的应用增加,特别是雄激素受体靶向(ARAT)治疗的应用增加。接受 ADT 单药治疗的患者年龄较大,合并症更多,转移性疾病部位更少,且使用阿片类药物的可能性较小。
在本研究中,我们表明接受 ADT 单药治疗 mCSPC 的患者年龄较大,合并症较多,疾病范围较小。虽然随着时间的推移,接受 ADT 单药治疗的患者数量有所下降,但仍有超过 50%的 mCSPC 患者继续接受 ADT 单药治疗。需要进一步研究以了解治疗强化的障碍,并开展知识转化举措,以改善 mCSPC 患者的治疗。