Upgrading and downgrading of prostate needle biopsy specimens: Risk factors and clinical implications

被引:150
作者
Freedland, Stephen J.
Kane, Christopher J.
Amling, Christopher L.
Aronson, William J.
Terris, Martha K.
Presti, Joseph C., Jr.
机构
[1] Durham Vet Affairs Med Ctr, Dept Surg, Durham, NC USA
[2] Duke Univ, Sch Med, Div Urol Surg, Dept Surg, Durham, NC USA
[3] Duke Univ, Sch Med, Div Urol Surg, Dept Pathol, Durham, NC USA
[4] Duke Univ, Sch Med, Duke Prostate Ctr, Durham, NC USA
[5] San Francisco VA Med Ctr, Dept Surg, Urol Sect, San Francisco, CA USA
[6] Univ Calif San Francisco, Sch Med, Dept Urol, San Francisco, CA 94143 USA
[7] Univ Alabama, Dept Urol, Birmingham, AL USA
[8] San Diego Naval Hosp, Dept Urol, San Diego, CA USA
[9] Vet Affairs Greater Los Angeles Healthcare Syst, Dept Surg, Urol Sect, Los Angeles, CA USA
[10] Univ Calif Los Angeles, Sch Med, Dept Urol, Los Angeles, CA USA
[11] Med Coll Georgia, Augusta Vet Affairs Med Ctr, Dept Surg, Augusta, GA 30912 USA
[12] Stanford Univ, Sch Med, Dept Urol, Stanford, CA 94305 USA
[13] Vet Affairs Palo Alto Healthcare Syst, Dept Surg, Urol Sect, Palo Alto, CA USA
关键词
D O I
10.1016/j.urology.2006.10.036
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The prostate biopsy Gleason grade frequently differs from the radical prostatectomy (RP) grade. Given the critical role that needle biopsy plays in treatment decisions, we sought to determine the risk factors for upgrading and downgrading the prostate biopsy specimen. METHODS We determined the significant predictors of upgrading (worse RP grade than biopsy grade) and downgrading (better RP grade than biopsy grade) among 1113 men treated with RP from 1996 to 2005 within the Shared Equal Access Regional Cancer Hospital (SEARCH) database who had undergone at least sextant biopsy. The Gleason sum was examined as a categorical variable of 2 to 6, 3+4, and 4+3 or greater. RESULTS Overall, the disease of 299 men (27%) was upgraded and 123 (11%) was downgraded, and 691 men (62%) had identical biopsy and pathologic Gleason sum groups. Upgrading was associated with adverse pathologic features (P <= 0.001) and the risk of biochemical progression (P = 0.001). Downgrading was associated with more favorable pathologic features (P <= 0.01) and a decreased risk of progression (P = 0.04). On multivariate analysis, greater prostate-specific antigen levels (P < 0.001), more biopsy cores with cancer (P = 0.001), and obesity (P = 0.003) were all significantly and positively associated with upgrading. In contrast, biopsy Gleason sum 3+4 (P = 0.001) and obtaining eight or more biopsy cores (P = 0.01) were associated with a lower likelihood of upgrading. CONCLUSIONS Men whose disease was upgraded were at a greater risk of adverse pathologic features and biochemical progression. Men with "high-risk" cancer (greater prostate-specific antigen levels, more positive cores, and obese) were more likely to have their disease category upgraded, and obtaining more biopsy cores reduced the likelihood of upgrading.
引用
收藏
页码:495 / 499
页数:5
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