Raval Amit D, Zhang Yiqiao, Korn Matthew, Constantinovici Niculae, McKay Rana R
Bayer HealthCare Pharmaceuticals, Whippany, NJ, USA.
Bayer Consumer Care, Basel, Switzerland.
Prostate Cancer Prostatic Dis. 2025 Apr 4. doi: 10.1038/s41391-025-00969-6.
The treatment landscape for metastatic castration-resistant prostate cancer (mCRPC) has evolved since radium-223 (Ra-223) was approved in the United States (2013). We examined treatment patterns and real-world overall survival (rwOS) of men with mCRPC treated with Ra-223 in the modern treatment era.
A retrospective cohort of men treated with Ra-223 was derived using private insurance data from the Komodo Health dataset from January 1, 2017 to June 30, 2022. Cox-regression analyses examined associations between Ra-223 use and rwOS with adjustment for covariates.
Of 1376 men, the median age was 68 years, 51% were White, and 89% had bone-only metastases. Overall, 17%, 35%, and 25% of men received Ra-223 as first-line, second-line, or third-line treatment for mCRPC, respectively. Thirty-six percent received Ra-223 as combination/layered therapy, mainly with enzalutamide, and 46% completed ≥5 cycles. Overall, median rwOS was 22.9 months. Median rwOS was longer in men who completed ≥5 Ra-223 cycles versus 1-4 cycles (30.3 versus 15.3 months) and combination/layered therapy versus monotherapy (26.6 versus 20.5 months). Combination/layered therapy and completion of ≥5 Ra-223 cycles were associated with 22% and 55% reductions in risk of death in adjusted analyses, respectively. Limitations include some clinical information not captured by claims databases.
Significant rwOS benefits were identified in men who received Ra-223 as an earlier line of therapy, received Ra-223 in combination with another therapy, and completed ≥5 Ra-223 cycles, underscoring the importance of Ra-223 in the current treatment landscape.
自镭-223(Ra-223)于2013年在美国获批以来,转移性去势抵抗性前列腺癌(mCRPC)的治疗格局不断演变。我们研究了在现代治疗时代接受Ra-223治疗的mCRPC男性患者的治疗模式和真实世界总生存期(rwOS)。
利用2017年1月1日至2022年6月30日来自科莫多健康数据集的私人保险数据,建立了一个接受Ra-223治疗的男性回顾性队列。Cox回归分析在对协变量进行调整的情况下,研究了Ra-223使用与rwOS之间的关联。
在1376名男性中,中位年龄为68岁,51%为白人,89%仅有骨转移。总体而言,分别有17%、35%和25%的男性将Ra-223作为mCRPC的一线、二线或三线治疗。36%的患者接受Ra-223作为联合/分层治疗,主要与恩杂鲁胺联合使用,46%的患者完成了≥5个周期的治疗。总体而言,中位rwOS为22.9个月。完成≥5个Ra-223周期的男性的中位rwOS长于完成1-4个周期的男性(30.3个月对15.3个月),联合/分层治疗的男性的中位rwOS长于单药治疗的男性(26.6个月对20.5个月)。在调整分析中,联合/分层治疗和完成≥5个Ra-223周期分别与死亡风险降低22%和55%相关。局限性包括索赔数据库未获取一些临床信息。
在将Ra-223作为早期治疗线、与另一种疗法联合使用并完成≥5个Ra-223周期的男性中,发现了显著的rwOS获益,这突出了Ra-223在当前治疗格局中的重要性。