Long-term salvage radiotherapy outcome after radical prostatectomy and relapse predictors

被引:26
作者
Brooks, JP
Albert, PS
Wilder, RB
Gant, DA
McLeod, DG
Poggi, MM
机构
[1] USN, Div Radiat Oncol, Natl Med Ctr, Bethesda, MD 20889 USA
[2] Walter Reed Army Med Ctr, Dept Urol, Washington, DC 20307 USA
[3] Walter Reed Army Med Ctr, Sect Radiat Oncol, Washington, DC 20307 USA
[4] NCI, Biometr Res Branch, Bethesda, MD 20892 USA
关键词
prostate; prostatic neoplasms; radiation; prostatectomy; salvage therapy;
D O I
10.1097/01.ju.0000181223.99576.ff
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: We assessed the efficacy of salvage radiotherapy (SRT) and analyzed predictors of biochemical progression-free survival (bPFS) and distant metastasis-free survival in patients with clinically localized disease recurrence after radical prostatectomy. Materials and Methods: The records of 114 patients treated with SRT at 2 institutions between 1991 and 2001 were retrospectively reviewed. Time to biochemical recurrence and to distant metastases was analyzed using the Kaplan-Meier estimation. Candidate predictors of bPFS and distant metastasis-free survival were analyzed using the log rank test and Cox regression. Acute and late complications were scored using Radiation Therapy Oncology Group/European Organization for Research and Treatment of Cancer criteria. Results: At a median followup of 6.3 years (range 1.9 to 13.3) for SRT 4 and 6-year bPFS was 50% (95% CI 42% to 61%) and 33% (95% CI 24% to 43%), respectively. The 6-year actuarial probability of distant metastases after SRT was 14%. Multivariate analysis demonstrated an independent association of increasing Gleason score, lymphovascular invasion and lack of a complete response to SRT with decreased 5-year bDFS. These factors were associated with significantly less 5-year distant metastasis-free survival. Pre-RT prostate specific antigen greater than 2.0 ng/ml was associated with significantly decreased 5-year bDFS and distant metastasis-free survival, although it was not maintained on multivariate analysis. Conclusions: SRT results in durable prostate specific antigen control in select patients. It is well tolerated with few severe late effects. Increasing Gleason score, lymphovascular invasion and lack of a complete response to SRT are significant risks for disease progression requiring additional management.
引用
收藏
页码:2204 / 2208
页数:5
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