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Accuracy of biopsy Gleason scores from a large uropathology laboratory: use of a diagnostic protocol to minimize observer variability.

机译:大型泌尿病理学实验室活检的Gleason评分的准确性:使用诊断规程以最小化观察者的变异性。

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OBJECTIVES: To examine the correlation of biopsy Gleason scores with radical prostatectomy specimens from a laboratory that uses protocols designed to minimize observer variability. This protocol mandates consensus case review of all nonbenign cases. METHODS: Between August 24, 1993 and June 26, 1997, 106 patients who underwent radical prostatectomy at Johns Hopkins Hospital, Baltimore, Maryland had their prostate cancer diagnosed and graded at one laboratory (DIANON Systems). We analyzed the Gleason scores from the biopsy and radical prostatectomy specimens. RESULTS: Exact correlation existed between biopsy and radical prostatectomy Gleason scores for 72 (68%) cases; 103 (97%) correlated within 1 grade, all cases correlated within 2 grades; 26 (25%) biopsies were undergraded and 8 (8%) were overgraded. Positive predictive values for biopsy Gleason scores 5, 6, and 7 were 66%, 67%, and 71%, respectively. Grouped Gleason scores (well differentiated [2 to 4], moderately differentiated [5, 6], moderately to poorly differentiated [7], and poorly differentiated [8 to 10]) correlated exactly for 74 (70%) cases and within 1 group for all cases. Patient age, digital rectal examination results, total number of positive cores, and maximum percentage of tumor on biopsy did not affect correlation, but prostate-specific antigen (PSA) levels did affect correlation (exact correlation 96% when the PSA level was less than 5 ng/mL; 50% when the PSA level was 11 ng/mL or greater, P <0.01). CONCLUSIONS: The combination of experience and the protocol described minimizes intra- and interobserver variability, thereby improving the predictive value of biopsy Gleason grading. Biopsy and radical prostatectomy Gleason scores correlate more poorly when the PSA level is high (11 ng/mL or greater) than when the PSA level is low (less than 5 ng/mL).
机译:目的:为了检查活检格里森评分与根治性前列腺切除术标本的相关性,该实验室标本采用旨在最小化观察者变异的方案。该协议要求对所有非良性案例进行共识案例审查。方法:在1993年8月24日至1997年6月26日之间,在马里兰州巴尔的摩市约翰霍普金斯医院接受根治性前列腺切除术的106例患者在一个实验室(DIANON Systems)进行了前列腺癌的诊断和分级。我们分析了活检和前列腺癌根治术标本的格里森评分。结果:72例(68%)病例的活检与根治性前列腺切除术的格里森评分之间存在确切的相关性; 1个等级中有103个(97%)相关,而2个等级中所有情况都具有相关性; 26例(25%)的活组织检查被低估,8例(8%)的被高估。活检Gleason评分5、6和7的阳性预测值分别为66%,67%和71%。分组的Gleason评分(高分化[2至4],中分化[5、6],中至低分化[7]和低分化[8至10])与74(70%)例且在1组内准确相关对于所有情况。患者年龄,直肠指检结果,阳性核心总数和活检肿瘤的最大百分比均不影响相关性,但前列腺特异性抗原(PSA)水平确实影响相关性(当PSA水平低于90%时,准确相关性为96% 5 ng / mL;当PSA水平为11 ng / mL或更高时为50%,P <0.01)。结论:经验和描述的协议相结合,最大限度地减少了观察者之间和观察者之间的差异,从而提高了活检格里森分级的预测价值。当PSA水平高(11 ng / mL或更高)时,活检和根治性前列腺切除术的Gleason评分相关性比PSA水平低(小于5 ng / mL)时的相关性更差。

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