4.6 Article

Long-term overall survival and metastasis-free survival for men with prostate-specific antigen-recurrent prostate cancer after prostatectomy: analysis of the Center for Prostate Disease Research National Database

期刊

BJU INTERNATIONAL
卷 108, 期 3, 页码 378-385

出版社

WILEY
DOI: 10.1111/j.1464-410X.2010.09878.x

关键词

metastasis-free survival; natural history; overall survival; prostate cancer; PSA recurrence

资金

  1. Department of Defense
  2. Congressional Special Interest (CSI) biomedical research programme

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OBJECTIVE To describe metastasis-free survival (MFS) and overall survival (OS) among men with prostate-specific antigen (PSA)-recurrent prostate cancer after radical prostatectomy who did not receive additional therapy until metastasis, using a multicentre database capturing a wide ethnic mix. PATIENTS AND METHODS A retrospective analysis of the Center for Prostate Disease Research National Database (comprised of five US military hospitals and one civilian centre) was performed for patients with PSA relapse (>= 0.2 ng/mL) after radical prostatectomy who had no additional therapy until the time of radiographic metastatic disease. We investigated factors influencing metastasis and all-cause mortality using univariate and multivariate Cox regression analysis. RESULTS There were a total of 346 men who underwent radical prostatectomy between May 1983 and November 2008 and fulfilled the entry criteria. All patients had information on survival and 190 men had information on metastasis. Among patients with survival data (n = 346), 10-year OS was 79% after a median follow-up of 8.6 years from biochemical recurrence. Among men with metastasis data (n = 190), 10-year MFS was 46% after a median follow-up of 7.5 years. In Cox regressions, four clinical factors (Gleason score, pathological stage, time to PSA relapse and PSA doubling time), as well as age, were predictive of OS and/or MFS in univariate analysis, although only PSA doubling time (>= 9 vs 3-8.9 vs < 3 months) remained independently predictive of these outcomes in multivariate analysis (P < 0.001). CONCLUSIONS This multicentre multi-ethnic dataset shows that OS and MFS can be extensive for men with PSA-recurrent prostate cancer, even in the absence of further therapy before metastasis. This unique patient cohort, the second largest of its type after the Johns Hopkins cohort, confirms that PSA doubling time is the strongest determinant of OS and MFS in men with PSA-recurrent disease. Longer follow-up and more events will be required to determine whether other variables may also contribute to these outcomes.

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