Gleason grading and prognostic factors in carcinoma of the prostate

被引:349
作者
Humphrey, PA [1 ]
机构
[1] Washington Univ, Med Ctr, Dept Pathol & Immunol, Sch Med, St Louis, MO 63110 USA
关键词
prostate; cancer; Gleason grade; prognosis;
D O I
10.1038/modpathol.3800054
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Gleason grade of adenocarcinoma of the prostate is an established prognostic indicator that has stood the test of time. The Gleason grading method was devised in the 1960s and 1970s by Dr Donald F Gleason and members of the Veterans Administration Cooperative Urological Research Group. This grading system is based entirely on the histologic pattern of arrangement of carcinoma cells in H&E-stained sections. Five basic grade patterns are used to generate a histologic score, which can range from 2 to 10. These patterns are illustrated in a standard drawing that can be employed as a guide for recognition of the specific Gleason grades. Increasing Gleason grade is directly related to a number of histopathologic end points, including tumor size, margin status, and pathologic stage. Indeed, models have been developed that allow for pretreatment prediction of pathologic stage based upon needle biopsy Gleason grade, total serum prostate-specific antigen level, and clinical stage. Gleason grade has been linked to a number of clinical end points, including clinical stage, progression to metastatic disease, and survival. Gleason grade is often incorporated into nomograms used to predict response to a specific therapy, such as radiotherapy or surgery. Needle biopsy Gleason grade is routinely used to plan patient management and is also often one of the criteria for eligibility for clinical trials testing new therapies. Gleason grade should be routinely reported for adenocarcinoma of the prostate in all types of tissue samples. Experimental approaches that could be of importance in the future include determination of percentage of high-grade Gleason pattern 4 or 5, and utilization of markers discovered by gene expression profiling or by genetic testing for DNA abnormalities. Such markers would be of prognostic usefulness if they provided added value beyond the established indicators of Gleason grade, serum prostate-specific antigen, and stage. Currently, established prognostic factors for prostatic carcinoma recommended for routine reporting are TNM stage, surgical margin status, serum prostate-specific antigen, and Gleason grade.
引用
收藏
页码:292 / 306
页数:15
相关论文
共 63 条
[31]  
GLEASON DONALD F., 1966, CANCER CHEMO THERAP REP, V50, P125
[32]   Tumor marker utility grading system: A framework to evaluate clinical utility of tumor markers [J].
Hayes, DF ;
Bast, RC ;
Desch, CE ;
Fritsche, H ;
Kemeny, NE ;
Jessup, JM ;
Locker, GY ;
MacDonald, JS ;
Mennel, RG ;
Norton, L ;
Ravdin, P ;
Taube, S ;
Winn, RJ .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (20) :1456-1466
[33]  
Humphrey P., 2003, PROSTATE PATHOLOGY, P338
[34]   Prospective characterization of pathological features of prostatic carcinomas detected via serum prostate specific antigen based screening [J].
Humphrey, PA ;
Keetch, DW ;
Smith, DS ;
Shepherd, DL ;
Catalona, WJ .
JOURNAL OF UROLOGY, 1996, 155 (03) :816-820
[35]   INTRAGLANDULAR TUMOR EXTENT AND PROGNOSIS IN PROSTATIC-CARCINOMA - APPLICATION OF A GRID METHOD TO PROSTATECTOMY SPECIMENS [J].
HUMPHREY, PA ;
VOLLMER, RT .
HUMAN PATHOLOGY, 1990, 21 (08) :799-804
[36]   Pseudohyperplastic prostatic adenocarcinoma [J].
Humphrey, PA ;
Kaleem, Z ;
Swanson, PE ;
Vollmer, RT .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1998, 22 (10) :1239-1246
[37]   Postoperative nomogram for disease recurrence after radical prostatectomy for prostate cancer [J].
Kattan, MW ;
Wheeler, TM ;
Scardino, PT .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (05) :1499-1507
[38]   Patterns of treatment of patients with prostate cancer initially managed with surveillance: Results from the CaPSURE database [J].
Koppie, TM ;
Grossfeld, GD ;
Miller, D ;
Yu, J ;
Stier, D ;
Broering, JM ;
Lubeck, D ;
Henning, JM ;
Flanders, SC ;
Carroll, PR .
JOURNAL OF UROLOGY, 2000, 164 (01) :81-88
[39]  
Kronz JD, 2000, CANCER, V89, P1818, DOI 10.1002/1097-0142(20001015)89:8<1818::AID-CNCR23>3.3.CO
[40]  
2-A