Role of repeated biopsy of the prostate in predicting disease progression in patients with prostate cancer on active surveillance

被引:58
作者
Al Otaibi, Mohammed [1 ]
Ross, Philip [1 ]
Fahmy, Nader [1 ]
Jeyaganth, Suganthiny [1 ]
Trottier, Helen [2 ]
Sircar, Kanishka [3 ]
Begin, Louis R. [3 ]
Souhami, Luis [4 ]
Kassouf, Wassim [1 ]
Aprikian, Armen [1 ]
Tanguay, Simon [1 ]
机构
[1] McGill Univ, Ctr Hlth, Div Urol, Dept Surg, Montreal, PQ H3G 1A4, Canada
[2] McGill Univ, Ctr Hlth, Div Canc Epidemiol, Montreal, PQ H3G 1A4, Canada
[3] McGill Univ, Ctr Hlth, Dept Pathol, Montreal, PQ H3G 1A4, Canada
[4] McGill Univ, Ctr Hlth, Dept Radiat Oncol, Montreal, PQ H3G 1A4, Canada
关键词
prostate cancer; active surveillance; prostatic biopsy; disease progression;
D O I
10.1002/cncr.23575
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Active surveillance (AS) with deferred treatment is an established management option for patients with prostate cancer and favorable clinical parameters. The impact of repeat biopsy after diagnosis was examined in a cohort of men with prostate cancer on AS. METHODS. In all, 186 men with prostate cancer with favorable parameters or who refused treatment were conservatively managed by AS. Of these, 92 patients had at least I biopsy after diagnosis. Patients were followed every 3 to 6 months with prostate-specific antigen (PSA) and physical examination and were offered rebiopsy annually or if there were any changes on physical examination or in the PSA value. Disease progression while on AS was defined as having >= 1 of the following: >= cT2b disease, >= 3 positive cores, >50% of cancer in at least I core, or a predominant Gleason pattern of 4 in rebiopsies. RESULTS. The median age of the patients at the time of diagnosis was 67 years (range, 49-78 years). The median follow-up was 76 months (range, 20-169 months). Of the 92 patients who underwent repeat biopsies, 42 patients, 25 patients, 13 patients, 10 patients, and 2 patients had 1, 2, 3, 4, and 5 rebiopsies, respectively. A total of 34 patients (36%) demonstrated disease progression on rebiopsy. The first rebiopsy was positive for cancer in 48 patients (52.2%) and negative in 44 patients (47.8%). The 5-year actuarial progression-free probability was 82% for patients with a negative first repeat biopsy compared with 50% for patients with a positive first rebiopsy (P = .02). A PSA doubling time <67 months was associated an increased risk of disease progression on biopsy. CONCLUSIONS. Negative rebiopsy in patients with prostate cancer on AS is associated with low-volume disease. The result of first repeated biopsy appears to have a strong impact on disease progression. Patients with a positive first repeated biopsy should be considered for treatment. An intensive biopsy protocol within the first 2 years is required to identify and treat those patients.
引用
收藏
页码:286 / 292
页数:7
相关论文
共 27 条
[1]  
[Anonymous], J UROL 2
[2]   LATENT CARCINOMA OF PROSTATE AT AUTOPSY IN 7 AREAS - COLLABORATIVE STUDY ORGANIZED BY INTERNATIONAL-AGENCY-FOR-RESEARCH-ON-CANCER, LYONS, FRANCE [J].
BRESLOW, N ;
CHAN, CW ;
DHOM, G ;
DRURY, RAB ;
FRANKS, LM ;
GELLEI, B ;
LEE, YS ;
LUNDBERG, S ;
SPARKE, B ;
STERNBY, NH ;
TULINIUS, H .
INTERNATIONAL JOURNAL OF CANCER, 1977, 20 (05) :680-688
[3]   Expectant management of nonpalpable prostate cancer with curative intent: Preliminary results [J].
Carter, HB ;
Walsh, PC ;
Landis, P ;
Epstein, JI .
JOURNAL OF UROLOGY, 2002, 167 (03) :1231-1234
[4]   RESULTS OF CONSERVATIVE MANAGEMENT OF CLINICALLY LOCALIZED PROSTATE-CANCER [J].
CHODAK, GW ;
THISTED, RA ;
GERBER, GS ;
JOHANSSON, JE ;
ADOLFSSON, J ;
JONES, GW ;
CHISHOLM, GD ;
MOSKOVITZ, B ;
LIVNE, PM ;
WARNER, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (04) :242-248
[5]   THE ROLE OF WATCHFUL WAITING IN THE MANAGEMENT OF LOCALIZED PROSTATE-CANCER [J].
CHODAK, GW .
JOURNAL OF UROLOGY, 1994, 152 (05) :1766-1768
[6]   Feasibility study: Watchful waiting for localized low to intermediate grade prostate carcinoma with selective delayed intervention based on prostate specific antigen, histological and/or clinical progression [J].
Choo, R ;
Klotz, L ;
Danjoux, C ;
Morton, GC ;
DeBoer, G ;
Szumacher, E ;
Fleshner, N ;
Bunting, P ;
Hruby, G .
JOURNAL OF UROLOGY, 2002, 167 (04) :1664-1669
[7]   PSA doubling time of prostate carcinoma managed with watchful observation alone [J].
Choo, R ;
DeBoer, G ;
Klotz, L ;
Danjoux, C ;
Morton, GC ;
Rakovitch, E ;
Fleshner, N ;
Bunting, P ;
Kapusta, L ;
Hruby, G .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 50 (03) :615-620
[8]   Prostate cancer characteristics and prostate specific antigen changes in screening detected patients initially treated with a watchful waiting policy [J].
de Vries, SH ;
Raaijmakers, R ;
Kranse, R ;
Blijenberg, BG ;
Schröder, FH .
JOURNAL OF UROLOGY, 2004, 172 (06) :2193-2196
[9]   The role of serial free/total prostate-specific antigen ratios in a watchful observation protocol for men with localized prostate cancer [J].
Do, V ;
Choo, R ;
De Boer, G ;
Klotz, L ;
Danjoux, C ;
Morton, G ;
Szumacher, E ;
Fleshner, N ;
Bunting, P .
BJU INTERNATIONAL, 2002, 89 (07) :703-709
[10]   PATHOLOGICAL AND CLINICAL FINDINGS TO PREDICT TUMOR EXTENT OF NONPALPABLE (STAGE-T1C) PROSTATE-CANCER [J].
EPSTEIN, JI ;
WALSH, PC ;
CARMICHAEL, M ;
BRENDLER, CB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1994, 271 (05) :368-374