Prognostic factors in prostate cancer

被引:0
作者
A Buhmeida
S Pyrhönen
M Laato
Y Collan
机构
[1] Turku University Hospital,Departments of Oncology and Radiotherapy
[2] Turku University Hospital,Departments of Pathology
[3] Turku University Hospital,Departments of Surgery
来源
Diagnostic Pathology | / 1卷
关键词
Prostate Cancer; Prostate Specific Antigen; Radical Prostatectomy; Gleason Score; Localize Prostate Cancer;
D O I
暂无
中图分类号
学科分类号
摘要
Prognostic factors in organ confined prostate cancer will reflect survival after surgical radical prostatectomy. Gleason score, tumour volume, surgical margins and Ki-67 index have the most significant prognosticators. Also the origins from the transitional zone, p53 status in cancer tissue, stage, and aneuploidy have shown prognostic significance. Progression-associated features include Gleason score, stage, and capsular invasion, but PSA is also highly significant. Progression can also be predicted with biological markers (E-cadherin, microvessel density, and aneuploidy) with high level of significance. Other prognostic features of clinical or PSA-associated progression include age, IGF-1, p27, and Ki-67. In patients who were treated with radiotherapy the survival was potentially predictable with age, race and p53, but available research on other markers is limited. The most significant published survival-associated prognosticators of prostate cancer with extension outside prostate are microvessel density and total blood PSA. However, survival can potentially be predicted by other markers like androgen receptor, and Ki-67-positive cell fraction. In advanced prostate cancer nuclear morphometry and Gleason score are the most highly significant progression-associated prognosticators. In conclusion, Gleason score, capsular invasion, blood PSA, stage, and aneuploidy are the best markers of progression in organ confined disease. Other biological markers are less important. In advanced disease Gleason score and nuclear morphometry can be used as predictors of progression. Compound prognostic factors based on combinations of single prognosticators, or on gene expression profiles (tested by DNA arrays) are promising, but clinically relevant data is still lacking.
引用
收藏
相关论文
共 814 条
[1]  
Badalament RA(1991)Prostate cancer Dis Mon 37 199-268
[2]  
Drago JR(1992)Geographic patterns of prostate cancer mortality. Evidence for a protective effect of ultraviolet radiation Cancer 70 2861-2869
[3]  
Hanchette CL(2001)Cancer statistics, 2001 CA Cancer J Clin 51 15-36
[4]  
Schwartz GG(1996)Molecular biology of prostate cancer World J Urol 14 318-328
[5]  
Greenlee RT(2003)Prostate cancer Cooper DN (editor) 4 743-757
[6]  
Hill-Harmon MB(2004)Molecular pathology of prostate cancer: the key to identifying new biomarkers of disease Endocr Relat Cancer 11 477-88
[7]  
Murray T(2004)Whole genome scanning identifies genotypes associated with recurrence and metastasis in prostate tumours Hum Mol Genet 13 1303-1313
[8]  
Thun M(1995)Genetic characteristics of prostate cancer Cancer Epidemiol Biomarkers Prev 4 681-687
[9]  
Shi XB(2000)Molecular cytogenetics of prostate cancer Microsc Res Tech 51 456-463
[10]  
Gumerlock PH(2001)5q11, 8p11 and 10q22 are recurrent chromosomal breakpoints in prostate cancer cell lines Genes Chromosomes Cancer 30 187-195