Predictors of secondary treatment following biochemical recurrence after radical prostatectomy: results from the Shared Equal Access Regional Cancer Hospital database

被引:21
作者
Moreira, Daniel M. [1 ,2 ,3 ]
Banez, Lionel L. [1 ,2 ,3 ]
Presti, Joseph C., Jr. [5 ,6 ]
Aronson, William J. [7 ,8 ]
Terris, Martha K. [9 ,10 ]
Kane, Christopher J. [11 ]
Amling, Christopher L. [12 ,13 ]
Freedland, Stephen J. [1 ,2 ,3 ,4 ]
机构
[1] Duke Univ, Div Urol Surg, Sch Med, Dept Surg, Durham, NC 27710 USA
[2] Duke Univ, Duke Prostate Ctr, Sch Med, Durham, NC 27710 USA
[3] Vet Affairs Med Ctr, Urol Sect, Durham, NC USA
[4] Duke Univ, Dept Pathol, Sch Med, Durham, NC 27710 USA
[5] Stanford Univ, Med Ctr, Dept Urol, Palo Alto, CA 94304 USA
[6] Vet Affairs Med Ctr, Urol Sect, Dept Surg, Palo Alto, CA 94304 USA
[7] Vet Affairs Med Ctr, Urol Sect, Dept Surg, Los Angeles, CA USA
[8] Univ Calif Los Angeles, Med Ctr, Dept Urol, Los Angeles, CA 90024 USA
[9] Vet Affairs Med Ctr, Urol Sect, Dept Surg, Augusta, GA USA
[10] Med Coll Georgia, Dept Surg, Div Urol Surg, Augusta, GA 30912 USA
[11] Univ Calif San Diego, Med Ctr, Dept Surg, Div Urol, San Diego, CA 92103 USA
[12] Univ Alabama, Dept Surg, Div Urol, Birmingham, AL 35294 USA
[13] Vet Affairs Med Ctr, Urol Sect, Dept Surg, Birmingham, AL USA
关键词
prostate cancer; prostatectomy; radiotherapy; prostate-specific antigen; androgen; salvage therapy; combined therapy; antineoplastic agents; AFFAIRS MEDICAL-CENTERS; SEARCH DATABASE; GEOGRAPHIC-VARIATION; PATTERNS; THERAPY; OUTCOMES; SURVIVAL; FAILURE; CAPSURE; CARE;
D O I
10.1111/j.1464-410X.2009.08684.x
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
Level of Evidence 2b OBJECTIVE To investigate the predictors of secondary treatment for recurrent prostate cancer after radical prostatectomy (RP) among subjects from the Shared Equal Access Regional Cancer Hospital (SEARCH) database. PATIENTS AND METHODS We used Kaplan-Meier curves and Cox proportional hazard models to identify factors associated with time to secondary treatment and type of secondary treatment received among 697 men who developed biochemical recurrence (BCR) after RP. RESULTS During a median follow-up of 45 months after BCR, 357 men received salvage treatment. The 1-, 3-, and 5-year risk of receiving any salvage treatment was 29% (95% confidence interval (CI) 26-33%), 48% (95%CI 44-52%), and 53% (95%CI 49-57%), respectively. In multivariate analysis, more recent year of recurrence, centre, shorter disease-free interval, and pathological high-grade disease (Gleason 8-10) predicted increased risk of salvage treatment (all P < 0.01). Predictors of specifically receiving radiotherapy were shorter disease-free interval, centre, and more recent year of BCR (all P < 0.001). Predictors of specifically receiving hormonal therapy were shorter disease-free interval, more recent year of BCR, centre, high Gleason score, and higher tumour stage (all P < 0.05). In a subset analysis of men with available prostate-specific antigen doubling time (PSADT) data, shorter PSADT predicted receipt of any salvage treatment as well as radiation and hormonal therapy separately. CONCLUSIONS Among men who recur after RP, salvage treatment was associated with disease severity, centre and year of BCR; patient-specific factors (race, body mass index and age) were not predictive of secondary treatment. Although patients are being treated more aggressively in contemporary years, the affect on long-term survival is unknown.
引用
收藏
页码:28 / 33
页数:6
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