Cancer Prevention Program, Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, Washington.
Department of Urology, University of Washington, Seattle.
JAMA. 2024 Jun 25;331(24):2084-2093. doi: 10.1001/jama.2024.6695.
Outcomes from protocol-directed active surveillance for favorable-risk prostate cancers are needed to support decision-making.
To characterize the long-term oncological outcomes of patients receiving active surveillance in a multicenter, protocol-directed cohort.
DESIGN, SETTING, AND PARTICIPANTS: The Canary Prostate Active Surveillance Study (PASS) is a prospective cohort study initiated in 2008. A cohort of 2155 men with favorable-risk prostate cancer and no prior treatment were enrolled at 10 North American centers through August 2022.
Active surveillance for prostate cancer.
Cumulative incidence of biopsy grade reclassification, treatment, metastasis, prostate cancer mortality, overall mortality, and recurrence after treatment in patients treated after the first or subsequent surveillance biopsies.
Among 2155 patients with localized prostate cancer, the median follow-up was 7.2 years, median age was 63 years, 83% were White, 7% were Black, 90% were diagnosed with grade group 1 cancer, and median prostate-specific antigen (PSA) was 5.2 ng/mL. Ten years after diagnosis, the incidence of biopsy grade reclassification and treatment were 43% (95% CI, 40%-45%) and 49% (95% CI, 47%-52%), respectively. There were 425 and 396 patients treated after confirmatory or subsequent surveillance biopsies (median of 1.5 and 4.6 years after diagnosis, respectively) and the 5-year rates of recurrence were 11% (95% CI, 7%-15%) and 8% (95% CI, 5%-11%), respectively. Progression to metastatic cancer occurred in 21 participants and there were 3 prostate cancer-related deaths. The estimated rates of metastasis or prostate cancer-specific mortality at 10 years after diagnosis were 1.4% (95% CI, 0.7%-2%) and 0.1% (95% CI, 0%-0.4%), respectively; overall mortality in the same time period was 5.1% (95% CI, 3.8%-6.4%).
In this study, 10 years after diagnosis, 49% of men remained free of progression or treatment, less than 2% developed metastatic disease, and less than 1% died of their disease. Later progression and treatment during surveillance were not associated with worse outcomes. These results demonstrate active surveillance as an effective management strategy for patients diagnosed with favorable-risk prostate cancer.
需要了解协议指导的主动监测对低危前列腺癌的长期肿瘤学结果,以支持决策。
描述多中心、协议指导队列中接受主动监测的患者的长期肿瘤学结局。
设计、地点和参与者:Canary 前列腺主动监测研究(PASS)是一项前瞻性队列研究,于 2008 年启动。通过 2022 年 8 月在 10 个北美中心招募了 2155 名患有低危前列腺癌且无既往治疗的男性患者。
前列腺癌的主动监测。
经首次或后续监测活检治疗后患者的活检分级重新分类、治疗、转移、前列腺癌死亡率、总死亡率和治疗后复发的累积发生率。
在 2155 名局限性前列腺癌患者中,中位随访时间为 7.2 年,中位年龄为 63 岁,83%为白人,7%为黑人,90%诊断为 1 级肿瘤组,中位前列腺特异性抗原(PSA)为 5.2ng/ml。诊断后 10 年,活检分级重新分类和治疗的发生率分别为 43%(95%CI,40%-45%)和 49%(95%CI,47%-52%)。有 425 名和 396 名患者在确认性或后续监测活检后接受了治疗(分别在诊断后 1.5 年和 4.6 年中位数),5 年复发率分别为 11%(95%CI,7%-15%)和 8%(95%CI,5%-11%)。21 名患者进展为转移性癌症,有 3 例前列腺癌相关死亡。诊断后 10 年估计的转移或前列腺癌特异性死亡率分别为 1.4%(95%CI,0.7%-2%)和 0.1%(95%CI,0%-0.4%);同期总死亡率为 5.1%(95%CI,3.8%-6.4%)。
在这项研究中,诊断后 10 年,49%的男性无进展或无治疗,不到 2%发生转移性疾病,不到 1%死于疾病。监测期间的晚期进展和治疗与较差的结局无关。这些结果表明主动监测是一种有效的管理策略,适用于诊断为低危前列腺癌的患者。