Short-term outcomes of the prospective multicentre 'Prostate Cancer Research International: Active Surveillance' study

被引:130
作者
van den Bergh, Roderick C. N. [1 ]
Vasarainen, Hanna [9 ]
van der Poel, Henk G. [3 ]
Vis-Maters, Jenneke J. [4 ]
Rietbergen, John B. [2 ]
Pickles, Tom [10 ]
Cornel, Erik B. [5 ]
Valdagni, Riccardo [11 ]
Jaspars, Joris J. [6 ]
van der Hoeven, John [7 ]
Staerman, Frederic [12 ]
Oomens, Eric H. G. M. [8 ]
Rannikko, Antti [9 ]
Roemeling, Stijn [1 ]
Steyerberg, Ewout W.
Roobol, Monique J. [1 ]
Schroder, Fritz H. [1 ]
Bangma, Chris H. [1 ]
机构
[1] Univ Med Ctr, Erasmus MC, Dept Urol, NL-3000 CA Rotterdam, Netherlands
[2] St Franciscus Hosp, Dept Urol, Rotterdam, Netherlands
[3] Antoni Van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Urol, Amsterdam, Netherlands
[4] Albert Schweitzer Hosp, Dept Urol, Dordrecht, Netherlands
[5] Hosp Grp Twente, Dept Urol, Hengelo, Netherlands
[6] Oosterschelde Hosp, Dept Urol, Goes, Netherlands
[7] Reinier de Graaf Hosp, Dept Urol, Delft, Netherlands
[8] Amphia Hosp, Dept Urol, Breda, Netherlands
[9] Univ Helsinki, Cent Hosp, Dept Urol, Helsinki, Finland
[10] British Columbia Canc Agcy, Radiat Program, Vancouver, BC V5Z 4E6, Canada
[11] Fdn IRCCS Inst Nazl Tumori, Sci Directorate, Prostate Program, Dept Urol, Milan, Italy
[12] Ctr Hosp Univ, Dept Urol, Reims, France
关键词
active surveillance; biopsy; outcomes; prostate cancer; PSA; watchful waiting; MANAGEMENT; BIOPSY; MEN; PROGRESSION; VALIDATION; ANTIGEN; ANXIETY; TRIAL; GRADE;
D O I
10.1111/j.1464-410X.2009.08887.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
OBJECTIVE To evaluate the short-term outcomes of the prospective international Prostate Cancer Research International: Active Surveillance ('PRIAS') study (Dutch Trial Register NTR1718), as active surveillance (AS) for early prostate cancer might provide a partial solution to the current overtreatment dilemma in this disease. PATIENTS AND METHODS The first 500 (of > 950) participants with asymptomatic T1c/T2 prostate cancer, with a prostate-specific antigen (PSA) level of < 10.0 ng/mL, a PSA density of < 0.2 ng/mL/mL, a Gleason score of < 3 + 3 = 6, and one or two positive biopsy cores, were analysed. The follow-up protocol consisted of frequent PSA measurements, digital rectal examinations, and standard repeat biopsies (the first after 1 year). The primary outcome is survival free of active therapy; the secondary endpoints are reasons for stopping AS, findings in 1-year repeat biopsies, and outcomes after radical prostatectomy (RP). RESULTS Patients were included between December 2006 and July 2008. The median (25-75th percentile) follow-up after diagnosis was 1.02 (0.6-1.5) years. The 2-year survival rate free from active therapy was 73%. Of the 82 men who changed to active therapy during the follow-up, 68 (83%) did so based on the protocol. Of the 261 repeat biopsies available for analysis, 90 (34%) showed no cancer, while 57 (22%) showed a Gleason score of > 6 or more than two positive biopsy cores. There was a relatively unfavourable PSA doubling time of 0-10 years in 53% (102/194) and 62% (33/53) of men with favourable and unfavourable re-biopsy results, respectively. After RP, four of 24 (17%) men had T3 disease and 12 (50%) had a Gleason score of > 6. CONCLUSION AS seems feasible, but mortality outcomes are unknown. A strict follow-up protocol including standard 1-year repeat biopsies resulted in a quarter of men stopping AS after 2 years.
引用
收藏
页码:956 / 962
页数:7
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