Faraj Sheila F, Bezerra Stephania M, Yousefi Kasra, Fedor Helen, Glavaris Stephanie, Han Misop, Partin Alan W, Humphreys Elizabeth, Tosoian Jeffrey, Johnson Michael H, Davicioni Elai, Trock Bruce J, Schaeffer Edward M, Ross Ashley E, Netto George J
Department of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland, United States of America.
GenomeDx Biosciences, Vancouver, British Columbia, Canada.
PLoS One. 2016 Jan 5;11(1):e0146189. doi: 10.1371/journal.pone.0146189. eCollection 2016.
In 2005, the International Society of Urological Pathology (ISUP) introduced several modifications to the original Gleason system that were intended to enhance the prognostic power of Gleason score (GS). The objective of this study was to clinically validate the 2005 ISUP Gleason grading system for its ability to detect metastasis. We queried our institutional RP database for men with NCCN clinically localized intermediate to high-risk disease undergoing radical prostatectomy (RP) between 1992 and 2010 with no additional treatment until the time of metastatic progression. A case-cohort design was utilized. A total of 333 available RP samples were re-reviewed and GS was reassigned per the 2005 ISUP Gleason system. Cumulative incidence of metastasis was 0%, 8.4%, 24.5% and 44.4% among specimens that were downgraded, unchanged, had one point GS increase and two point GS increase, respectively. The hazard ratio for metastasis raised in GS 8 and 9 compared to GS 7 from 2.77 and 5.91 to 3.49 and 9.31, respectively. The survival c-index of GS increased from 0.70 to 0.80 when samples were re-graded at 5 years post RP. The c-index of the reassigned GS was higher than the original GS (0.77 vs 0.64) for predicting PCSM at 10 years post RP. The regraded GS improved the prediction of metastasis and PCSM. This validates the updated Gleason grading system using an unambiguous clinical endpoint and highlights the need for reassignment of Gleason grading according to 2005 ISUP system when considering comparisons of novel biomarkers to clinicopathological variables in archival cohorts.
2005年,国际泌尿病理学会(ISUP)对原有的 Gleason 系统进行了多项修改,旨在增强 Gleason 评分(GS)的预后预测能力。本研究的目的是对2005年 ISUP Gleason 分级系统检测转移的能力进行临床验证。我们查询了本机构的根治性前列腺切除术(RP)数据库,纳入1992年至2010年间接受 RP 治疗的 NCCN 临床局限性中高危疾病男性患者,在出现转移进展之前未接受其他治疗。采用病例队列设计。共重新评估了333份可用的 RP 样本,并根据2005年 ISUP Gleason 系统重新分配 GS。在分级降低、不变、GS 增加1分和 GS 增加2分的标本中,转移的累积发生率分别为0%、8.4%、24.5%和44.4%。与 GS 7相比,GS 8和 GS 9转移的风险比分别从2.77和5.91提高到3.49和9.31。RP 后5年重新分级时,GS 的生存 c 指数从0.70提高到0.80。重新分配的 GS 在预测 RP 后10年的前列腺癌特异性死亡率(PCSM)方面,其 c 指数高于原始 GS(分别为0.77和0.64)。重新分级的 GS 改善了对转移和 PCSM 的预测。这验证了使用明确临床终点的更新后的 Gleason 分级系统,并强调在考虑将新型生物标志物与存档队列中的临床病理变量进行比较时,需要根据2005年 ISUP 系统重新分配 Gleason 分级。