Does the Extent of Carcinoma in Prostatic Biopsies Predict Prostate-Specific Antigen Recurrence? A Systematic Review

被引:32
作者
Harnden, Patricia [1 ]
Shelley, Michael D. [2 ]
Naylor, Brian [3 ]
Coles, Bernadette [2 ]
Mason, Malcolm D. [4 ]
机构
[1] St James Univ Hosp, Canc Res UK Clin Ctr, Bexley Wing, Leeds LS9 7TF, W Yorkshire, England
[2] Velindre NHS Trust, Cochrane Urol Canc Unit, Cardiff CF14 2TL, S Glam, Wales
[3] Airedale Dist Gen Hosp, Keighley, Yorks, England
[4] Cardiff Univ, Cardiff CF10 1AA, S Glam, Wales
关键词
Prostate cancer; Biopsy prognostic factors; Tumour extent;
D O I
10.1016/j.eururo.2008.06.068
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
Context: The biologic potential of prostate cancer (pCA) is variable, and the ability to identify tumours that might cause morbidity and mortality is limited. Objective: This systematic review sought to establish whether measurement of tumour extent in biopsies provides additional prognostic information on the risk of disease progression. Evidence acquisition: A comprehensive 31-step search strategy was run in MEDLINE, EMBASE, and the Web of Knowledge (January 1990-July 2007) and supplemented by the hand-searching of references in retrieved articles and relevant journals to identify publications related to the measurement of the length of cancer in biopsies and biochemical or clinical recurrence or pCA death. Thirteen papers reporting on at least 100 patients were identified and included patients treated by watchful waiting or hormonal therapy (n = 1), radical prostatectomy (n = 11), or radiotherapy (n = 1). Only two studies reported on clinical progression or mortality. Sources of bias included patient selection and missing data resulting from the retrospective nature of the studies. Confounding factors included differences in biopsy strategies and measurement methods. Evidence synthesis: The percentage of cancer in biopsies (overall percentage or the greatest percentage in the most involved core) was an independent predictor of prostate-specific antigen (PSA) and clinical outcomes regardless of the form of treatment and was generally superior to simply counting the number of positive cores. The marked variability in study design, conduct, and reporting precluded meta-analysis of the data and precise risk estimation. Conclusions: Tumour quantitation is a promising prognostic tool in the assessment of risk of pCA progression. However, well-designed, population-based studies, controlling for confounding factors, are required to provide more accurate risk estimation and develop management strategies. This review highlights the need for new approaches in the assessment of pathologic prognostic factors to reach the level of evidence achieved in other areas of medical practice. (C) 2008 Published by Elsevier B.V. on behalf of European Association of Urology.
引用
收藏
页码:728 / 739
页数:12
相关论文
共 45 条
[11]   Current practice of diagnosis and reporting of prostate cancer on needle biopsy among genitourinary pathologists [J].
Egevad, L ;
Allsbrook, WC ;
Epstein, JI .
HUMAN PATHOLOGY, 2006, 37 (03) :292-297
[12]   Diagnostic value of systematic biopsy methods in the investigation of prostate cancer: A systematic review [J].
Eichler, K ;
Hempel, S ;
Wilby, J ;
Myers, L ;
Bachmann, LM ;
Kleijnen, J .
JOURNAL OF UROLOGY, 2006, 175 (05) :1605-1612
[13]   Preoperative model for predicting prostate specific antigen recurrence after radical prostatectomy using percent of biopsy tissue with cancer, biopsy Gleason grade and serum prostate specific antigen [J].
Freedland, SJ ;
Terris, MK ;
Csathy, GS ;
Kane, CJ ;
Amling, CL ;
Presti, JC ;
Dorey, F ;
Aronson, WJ .
JOURNAL OF UROLOGY, 2004, 171 (06) :2215-2220
[14]   The percentage of prostate needle biopsy cores with carcinoma from the more involved side of the biopsy as a predictor of prostate specific antigen recurrence after radical prostatectomy - Results from the shared equal access regional cancer hospital (SEARCH) database [J].
Freedland, SJ ;
Aronson, WJ ;
Terris, MK ;
Kane, CJ ;
Amling, CL ;
Dorey, F ;
Presti, JC .
CANCER, 2003, 98 (11) :2344-2350
[15]   Comparison of percentage of total prostate needle biopsy tissue with cancer to percentage of cores with cancer for predicting PSA recurrence after radical prostatectomy: Results from the search database [J].
Freedland, SJ ;
Aronson, WJ ;
Csathy, GS ;
Kane, CJ ;
Amling, CL ;
Presti, JC ;
Dorey, F ;
Terris, MK .
UROLOGY, 2003, 61 (04) :742-747
[16]  
Fröhner M, 2006, EUR UROL, V50, P926
[17]  
Gambacorta M Antonietra, 2005, Rays, V30, P181
[18]   Using the percentage of biopsy cores positive for cancer, pretreatment PSA, and highest biopsy Gleason sum to predict pathologic stage after radical prostatectomy: The center for prostate disease research nomograms [J].
Gancarczyk, KJ ;
Wu, HY ;
McLeod, DG ;
Kane, C ;
Kusuda, L ;
Lance, R ;
Herring, J ;
Foley, J ;
Baldwin, D ;
Bishoff, JT ;
Soderdahl, D ;
Moul, JW .
UROLOGY, 2003, 61 (03) :589-595
[19]   Substratification of Stage T1c prostate cancer based on the probability of biochemical recurrence [J].
Gretzer, MB ;
Epstein, JI ;
Pound, CR ;
Walsh, PC ;
Partin, AW .
UROLOGY, 2002, 60 (06) :1034-1039
[20]   Prostatic pathology reporting in the UK: development of a national external quality assurance scheme [J].
Harnden, P. ;
Coleman, D. ;
Moss, S. ;
Kodikara, S. ;
Patnick, J. ;
Melia, J. .
HISTOPATHOLOGY, 2008, 52 (02) :147-157