Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California, USA.
Department of Urology, Los Angeles Medical Center, Kaiser Permanente Southern California, Los Angeles, California, USA.
Cancer Rep (Hoboken). 2023 Mar;6(3):e1749. doi: 10.1002/cnr2.1749. Epub 2022 Nov 8.
Few studies have evaluated the effect of statin exposure on metastasis risk among prostate cancer patients not receiving curative treatment.
We included men diagnosed with localized prostate cancer at an integrated health care system between 1997 and 2006 who did not receive curative treatment within 6 months of diagnosis. We followed these men until a metastatic event, disenrollment, death, or 12/31/2016. We collected all data from electronic health records supplemented by chart review. We used Cox regressions to examine the association between post-diagnostic statin exposure and metastasis, controlling for clinical characteristics and pre-diagnostic statin exposure.
There were 4245 men included. Mean age of diagnosis was 68.02 years. 46.6% of men used statins after prostate cancer diagnosis. During follow-up, 192 men developed metastasis (cumulative incidence rate: 14.5%). In the adjusted Cox model, statin use post-prostate cancer diagnosis was not significantly associated with a metastatic event (HR = 0.97, 95% CI = 0.69, 1.36). Pre-diagnostic statin use was also not associated with development of metastasis (HR = 0.76, 95% CI = 0.53, 1.10). We did not observe a dose-response for the proportion of person-time at-risk post-prostate cancer diagnosis on statins (HR = 0.98 per 10% increase in person-time exposed [95% CI = 0.93, 1.03]).
We did not find an inverse association between post-diagnosis statin exposure and metastasis development in localized prostate cancer patients who did not receive active treatment. Our results did not offer support to the chemopreventive potential of post-diagnostic statin use among men on active surveillance.
很少有研究评估在未接受根治性治疗的前列腺癌患者中,他汀类药物暴露对转移风险的影响。
我们纳入了 1997 年至 2006 年在一个综合医疗保健系统中被诊断为局限性前列腺癌且在诊断后 6 个月内未接受根治性治疗的男性。我们对这些男性进行随访,直到发生转移事件、退出、死亡或 2016 年 12 月 31 日。我们从电子病历中收集所有数据,并通过病历回顾进行补充。我们使用 Cox 回归来检验诊断后他汀类药物暴露与转移之间的关系,同时控制临床特征和诊断前他汀类药物暴露。
共纳入 4245 名男性。诊断时的平均年龄为 68.02 岁。46.6%的男性在前列腺癌诊断后使用了他汀类药物。在随访期间,192 名男性发生了转移(累积发病率:14.5%)。在调整后的 Cox 模型中,前列腺癌诊断后使用他汀类药物与转移事件无显著相关性(HR=0.97,95%CI=0.69,1.36)。诊断前使用他汀类药物也与转移的发生无关(HR=0.76,95%CI=0.53,1.10)。我们没有观察到前列腺癌诊断后他汀类药物暴露的时间比例与发病风险之间存在剂量反应关系(HR=0.98,每增加 10%的暴露时间风险比例增加 0.93[95%CI=0.93,1.03])。
我们没有发现在未接受积极治疗的局限性前列腺癌患者中,诊断后他汀类药物暴露与转移发展之间存在负相关关系。我们的结果并没有为在接受主动监测的男性中使用诊断后他汀类药物的化学预防潜力提供支持。