Prostate biopsy grading errors: A sampling problem?

Authors
Citation
Cr. King et Jp. Long, Prostate biopsy grading errors: A sampling problem?, INT J CANC, 90(6), 2000, pp. 326-330
Citations number
17
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF CANCER
ISSN journal
00207136 → ACNP
Volume
90
Issue
6
Year of publication
2000
Pages
326 - 330
Database
ISI
SICI code
0020-7136(200012)90:6<326:PBGEAS>2.0.ZU;2-I
Abstract
Potential reasons for discordance between the Gleason score in biopsies and surgical specimens are: 1) pathological interpretation bias, and 2) sampli ng effects. The importance of sampling effects in grading errors was examin ed in a series where the number of biopsy cores obtained was high. Biopsies were obtained using a technique whereby 18 directed cores were systematica lly obtained and mapped out within the gland. Gleason scores from biopsies and matched prostatectomy specimens were compared among 28 consecutive pati ents with localized prostate cancer. A pooled database from 10 series (n = 2,687) served as a baseline for comparison in the accuracy of Gleason score grading. With the present biopsy technique, an exact Gleason score match w as achieved in 57% of cases, compared with the pooled database (PD) mean of 42% (P = 0.055), and was within I point in 93% of cases compared with 78% (PD) (P = 0.029). Upgrading of biopsies was seen in 35% of cases, compared with 43% (PD) (P = 0.19). With respect to Gleason score 7, an exact match w as present in 78% of cases, compared with 63% (PD) (P = 0.17), and upgradin g was 0%, compared with 20% (PD) (P = 0.07). The data suggest a significant reduction in grade errors by minimizing sampling effects, one that it is o f the same order of magnitude as the reduction achieved from consensus path ologic evaluation. In our study, seven patients (25%) would have had their cancers missed altogether with sextant biopsies. Sampling effects may contr ibute significantly to grading errors in prostate needle biopsies, although a larger study is needed to confirm this. A methodology which adopts a hig her number of cores combined with a consensus pathologic evaluation could p otentially reduce grading errors substantially. The optimal number of cores remains to be determined in a larger study. Int. J. Cancer (Radiat. Oncol. Invest.) 90, 326-340 (2000). (C) 2000 Wiley-Liss, Inc.