A Multi-institutional Evaluation of Active Surveillance for Low Risk Prostate Cancer

被引:82
作者
Eggener, Scott E. [1 ]
Mueller, Alex
Berglund, Ryan K.
Ayyathurai, Raj [2 ,3 ]
Soloway, Cindy [2 ]
Soloway, Mark S. [2 ]
Abouassaly, Robert
Klein, Eric A. [3 ]
Jones, Steven J. [3 ]
Zappavigna, Chris [4 ]
Goldenberg, Larry [4 ]
Scardino, Peter T.
Eastham, James A.
Guillonneau, Bertrand
机构
[1] Univ Chicago, Chicago, IL 60637 USA
[2] Univ Miami, Miami, FL USA
[3] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[4] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
基金
美国国家卫生研究院;
关键词
prostatic neoplasms; biopsy; treatment outcome; THERAPY; MEN; PROBABILITY; EXPERIENCE; MANAGEMENT; TIME;
D O I
10.1016/j.juro.2008.11.109
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: For select men with low risk prostate cancer active surveillance is more often being considered a management strategy. In a multicenter retrospective study we evaluated the actuarial rates and predictors of remaining on active surveillance, the incidence of cancer progression and the pathological findings of delayed radical prostatectomy. Materials and Methods: A cohort of 262 men from 4 institutions met the inclusion criteria of age 75 years or younger, prostate specific antigen 10 ng/ml or less, clinical stage T1-T2a, biopsy Gleason sum 6 or less, 3 or less positive cores at diagnostic biopsy, repeat biopsy before active surveillance and no treatment for 6 months following the repeat biopsy. Active surveillance started on the date of the second biopsy. Actuarial rates of remaining on active surveillance were calculated and univariate Cox regression was used to assess predictors of discontinuing active surveillance. Results: With a median followup of 29 months 43 patients ultimately received active treatment. The 2 and 5-year probabilities of remaining on active surveillance were 91% and 75%, respectively. Patients with cancer on the second biopsy (HR 2.23, 95% CI 1.23-4.06, p = 0.007) and a higher number of cancerous cores from the 2 biopsies combined (p = 0.002) were more likely to undergo treatment. Age, prostate specific antigen, clinical stage, prostate volume and number of total biopsy cores sampled were not predictive of outcome. Skeletal metastases developed in 1 patient 38 months after starting active surveillance. Of the 43 patients undergoing delayed treatment 41 (95%) are without disease progression at a median of 23 months following treatment. Conclusions: With a median followup of 29 months active surveillance for select patients appears to be safe and associated with a low risk of systemic progression. Cancer at restaging biopsy and a higher total number of cancerous cores are associated with a lower likelihood of remaining on active surveillance. A restaging biopsy should be strongly considered to finalize eligibility for active surveillance.
引用
收藏
页码:1635 / 1641
页数:7
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