Delahunt B, Egevad L, Srigley J R, Steigler A, Murray J D, Atkinson C, Matthews J, Duchesne G, Spry N A, Christie D, Joseph D, Attia J, Denham J W
1Department of Pathology and Molecular Medicine, Wellington School of Medicine and Health Sciences, Wellington, New Zealand 2Department of Oncology - Pathology, Karolinska Institute, Stockholm, Sweden 3Department of Pathology and Molecular Medicine, McMaster University, Toronto, Canada 4School of Medicine and Public Health, University of Newcastle, Newcastle, NSW, Australia 5St Georges Cancer Care Centre, Christchurch 6Auckland Hospital, Auckland, New Zealand 7Peter MacCallum Cancer Centre, Melbourne, Vic 8Sir Charles Gairdner Hospital, Perth, WA 9Genesis Care, Tugun, Qld 10Hunter Medical Research Institute, Newcastle, NSW, Australia.
Pathology. 2015 Oct;47(6):520-5. doi: 10.1097/PAT.0000000000000318.
In 2014 a consensus conference convened by the International Society of Urological Pathology (ISUP) adopted amendments to the criteria for Gleason grading and scoring (GS) for prostatic adenocarcinoma. The meeting defined a modified grading system based on 5 grading categories (grade 1, GS 3+3; grade 2, GS 3+4; grade 3, GS 4+3; grade 4, GS 8; grade 5, GS 9-10). In this study we have evaluated the prognostic significance of ISUP grading in 496 patients enrolled in the TROG 03.04 RADAR Trial. There were 19 grade 1, 118 grade 2, 193 grade 3, 88 grade 4 and 79 grade 5 tumours in the series, with follow-up for a minimum of 6.5 years. On follow-up 76 patients experienced distant progression of disease, 171 prostate specific antigen (PSA) progression and 39 prostate cancer deaths. In contrast to the 2005 modified Gleason system (MGS), the hazards of the distant and PSA progression endpoints, relative to grade 2, were significantly greater for grades 3, 4 and 5 of the 2014 ISUP grading scheme. Comparison of predictive ability utilising Harrell's concordance index, showed 2014 ISUP grading to significantly out-perform 2005 MGS grading for each of the three clinical endpoints.
2014年,国际泌尿病理学会(ISUP)召开了一次共识会议,通过了前列腺腺癌Gleason分级和评分(GS)标准的修订案。该会议定义了一种基于5个分级类别的改良分级系统(1级,GS 3+3;2级,GS 3+4;3级,GS 4+3;4级,GS 8;5级,GS 9-10)。在本研究中,我们评估了ISUP分级在496例参与TROG 03.04 RADAR试验的患者中的预后意义。该系列中有19例1级肿瘤、118例2级肿瘤、193例3级肿瘤、88例4级肿瘤和79例5级肿瘤,随访时间至少为6.5年。随访期间,76例患者出现疾病远处进展,171例出现前列腺特异性抗原(PSA)进展,39例死于前列腺癌。与2005年改良Gleason系统(MGS)相比,2014年ISUP分级方案中3级、4级和5级相对于2级的远处和PSA进展终点的风险显著更高。利用Harrell一致性指数进行预测能力比较,结果显示2014年ISUP分级在三个临床终点上均显著优于2005年MGS分级。