Klotz Laurence H
Division of Urology, Sunnybrook & Women's College Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
Can J Urol. 2005 Feb;12 Suppl 1:53-7; discussion 101-2.
To summarize the case for active surveillance for good risk prostate cancer with selective delayed intervention for rapid biochemical or grade progression, and review the results of a large phase II experience using this approach.
A prospective phase II study of active surveillance with selective delayed intervention was initiated in 1995. Patients were managed initially with surveillance; those who had a PSA DT of 2 years or less, or grade progression on rebiopsy were offered radical intervention. The remainder were closely monitored.
The cohort consists of 299 patients with good risk prostate cancer, or intermediate risk prostate cancer in men over 70. The median PSA doubling time was 7.0 years. 35% had a PSA DT > 10 years. The majority of patients remain on surveillance. At 8 years, overall actuarial survival is 85%, and disease specific survival is 99%.
Most men with favorable risk prostate cancer will die of unrelated causes. The approach of active surveillance with selective delayed intervention based on PSA DT represents a practical compromise between radical therapy for all (which results in overtreatment for patients with indolent disease), and watchful waiting with palliative therapy only (which results in undertreatment for those with aggressive disease). The results at 8 years are favorable. Longer follow up will be required to confirm the safety of this approach in men with a long (>15 year) life expectancy.
总结对低风险前列腺癌进行主动监测并对快速生化进展或分级进展进行选择性延迟干预的情况,并回顾使用这种方法的大型II期研究结果。
1995年启动了一项关于主动监测并选择性延迟干预的前瞻性II期研究。患者最初接受监测;前列腺特异性抗原(PSA)倍增时间为2年或更短,或再次活检时出现分级进展的患者接受根治性干预。其余患者则进行密切监测。
该队列由299例低风险前列腺癌患者或70岁以上的中风险前列腺癌患者组成。PSA中位倍增时间为7.0年。35%的患者PSA倍增时间>10年。大多数患者仍在接受监测。8年时,总精算生存率为85%,疾病特异性生存率为99%。
大多数低风险前列腺癌男性将死于无关原因。基于PSA倍增时间进行主动监测并选择性延迟干预的方法是一种实际的折衷方案,介于对所有患者进行根治性治疗(这会导致对惰性疾病患者过度治疗)和仅进行观察等待及姑息治疗(这会导致对侵袭性疾病患者治疗不足)之间。8年的结果是良好的。需要更长时间的随访来证实这种方法对预期寿命长(>15年)的男性的安全性。