Guimaraes Marbele S, Quintal Maisa M, Meirelles Luciana R, Magna Luis A, Ferreira Ubirajara, Billis Athanase
Department of Anatomic Pathology, School of Medicine, State University of Campinas (Unicamp), Campinas, SP, Brazil.
Int Braz J Urol. 2008 Jan-Feb;34(1):23-9. doi: 10.1590/s1677-55382008000100005.
There is evidence showing that Gleason grading of prostatic adenocarcinoma is one of the most powerful predictors of biological behavior and one of the most influential factors used to determine treatment for prostate cancer. The aim of the current study was to compare the Gleason score for needle biopsy to the Gleason score for the correspondent surgical specimen, find any possible difference in the biochemical (PSA) progression following surgery in upgraded cases, correlate Gleason score in the specimens to several clinicopathologic variables, and compare outcomes between patients with low-grade vs. high-grade Gleason and Gleason scores 3+4 vs. 4+3.
The study population consisted of 200 consecutive patients submitted to radical prostatectomy. Biochemical progression was defined as PSA > or = 0.2 ng/mL. Time to PSA progression was studied using the Kaplan-Meier product-limit analysis.
In 47.1% of the cases, there was an exact correlation and 40.6% of cases were underestimated in the biopsies. Half of the tumors graded Gleason 6 at biopsy were Gleason score 7 at surgery. These upgraded tumors had outcomes similar to tumors with Gleason score 7 in both biopsy and surgery. There was a positive correlation of high-grade Gleason score in the surgical specimens to higher preoperative PSA, more extensive tumors, positive margins and more advanced pathologic staging. Tumors with a Gleason score > or = 7 have lower PSA progression-free survival vs. Gleason scores < 7. In this series, there was no significant difference when comparing Gleason scores of 3+4 vs. 4+3.
The findings support the importance of Gleason grading for nomograms, which are used by clinicians to counsel individual patients and help them make important decisions regarding their disease.
有证据表明,前列腺腺癌的Gleason分级是生物学行为最有力的预测指标之一,也是用于确定前列腺癌治疗方案的最具影响力的因素之一。本研究的目的是比较穿刺活检的Gleason评分与相应手术标本的Gleason评分,找出升级病例术后生化(PSA)进展的任何可能差异,将标本中的Gleason评分与几个临床病理变量相关联,并比较低级别与高级别Gleason评分以及Gleason评分3+4与4+3患者的预后。
研究人群包括200例连续接受根治性前列腺切除术的患者。生化进展定义为PSA≥0.2 ng/mL。使用Kaplan-Meier乘积限分析研究PSA进展时间。
在47.1%的病例中,活检结果与手术标本完全相关,40.6%的病例在活检中被低估。活检时Gleason评分为6级的肿瘤,一半在手术时Gleason评分为7级。这些升级的肿瘤在活检和手术中的预后与Gleason评分为7级的肿瘤相似。手术标本中高级别Gleason评分与术前PSA水平较高、肿瘤范围更广、切缘阳性及病理分期更晚呈正相关。Gleason评分≥7的肿瘤与Gleason评分<7的肿瘤相比,无PSA进展生存期更短。在本系列中,比较Gleason评分3+4与4+3时无显著差异。
这些发现支持了Gleason分级对列线图的重要性,临床医生使用列线图为个体患者提供咨询,并帮助他们就其疾病做出重要决策。