Gleason grading: past, present and future

• Published in: Histopathology Vol. 60; no. 1; pp. 75 - 86
• Main Authors: Delahunt, Brett, Miller, Rose J, Srigley, John R, Evans, Andrew J, Samaratunga, Hemamali
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01-01-2012; Wiley Subscription Services, Inc
• Subjects: Classification; Gleason; grade; Humans; International Society of Urological Pathology; Male; modified scoring; Neoplasm Grading - methods; Prognosis; Prostate - pathology; prostate adenocarcinoma; prostate-specific antigen; Prostatic Neoplasms - classification; Prostatic Neoplasms - diagnosis; Prostatic Neoplasms - pathology; radical prostatectomy; Reproducibility of Results; score; tertiary pattern; thin core biopsy; Tumors
• ISSN: 0309-0167; 1365-2559
• DOI: 10.1111/j.1365-2559.2011.04003.x

Delahunt B, Miller R J, Srigley J R, Evans A J & Samaratunga H 
(2012) Histopathology60, 75–86 
Gleason grading: past, present and future
In 1966 Donald Gleason developed his grading and scoring system for prostatic adenocarcinoma. This classification was refined in 1974 and gained almost universal acceptance, being classified as a category 1 prognostic parameter by the College of American Pathologists. Modifications to the classification were recommended at a conference convened by the International Society of Urological Pathology (ISUP) in 2005. This modified classification has resulted in a significant upgrading of tumours, although some studies have shown a greater concordance between needle biopsy and radical prostatectomy scores when compared to classical Gleason (CG) grading. The ISUP consensus conference recommended that for needle biopsies higher tertiary patterns should be incorporated into the final Gleason score, and this has been correlated with biochemical failure, tumour volume and mortality. Recently the validity of including cribriform glands as a component of Gleason pattern 3 has been questioned and it has been recommended that all tumours showing cribriform architecture should be classified as Gleason pattern 4. The recommendations arising from the 2005 Consensus Conference were largely unsupported by validating data, yet this new grading system has achieved widespread usage. It is unfortunate that recent suggestions for further modification are similarly lacking in supporting evidence. In view of this it is recommended that the Modified Gleason Scoring Classification should continue to be utilized in its original (2005) format and that any future alterations should be implemented only when mandated by tumour‐related outcome studies.