A novel predictor of clinical progression in patients on active surveillance for prostate cancer

被引:3
作者
Tan, Guan Hee [1 ,2 ,3 ]
Finelli, Antonio [1 ,2 ,3 ]
Ahmad, Ardalan [1 ,2 ,3 ]
Wettstein, Marian S. [1 ,2 ,3 ]
Chandrasekar, Thenappan [4 ]
Zlotta, Alexandre R. [1 ,2 ,3 ]
Fleshner, Neil E. [1 ,2 ,3 ]
Hamilton, Robert J. [1 ,2 ,3 ]
Kulkarni, Girish S. [1 ,2 ,3 ]
Ajib, Khaled [1 ,2 ,3 ]
Nason, Gregory [1 ,2 ,3 ]
Perlis, Nathan [1 ,2 ,3 ]
机构
[1] Univ Hlth Network, Princess Margaret Canc Enter, Div Urol, Toronto, ON, Canada
[2] Univ Hlth Network, Toronto Gen Hosp, Toronto, ON, Canada
[3] Univ Toronto, Div Urol, Toronto, ON, Canada
[4] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Dept Urol, Philadelphia, PA USA
来源
CUAJ-CANADIAN UROLOGICAL ASSOCIATION JOURNAL | 2019年 / 13卷 / 08期
关键词
FOLLOW-UP; RISK; OUTCOMES; BIOPSY; SELECTION; COHORT; MEN;
D O I
10.5489/cuaj.6122
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
Introduction: Active surveillance (AS) is standard of care in low-risk prostate cancer (PCa). This study describes a novel total cancer location (TCLo) density metric and aims to determine its performance in predicting clinical progression (CP) and grade progression (GP). Methods: This was a retrospective study of patients on AS after confirmatory biopsy (CBx). We excluded patients with Gleason >= 7 at CBx and <2 years followup. TCLo was the number of locations with positive cores at diagnosis (DBx) and CBx. TCLo density was TCLo/prostate volume (PV). CP was progression to any active treatment while GP occurred if Gleason >= 7 was identified on repeat biopsy or surgical pathology. Independent predictors of time to CP or GP were estimated with Cox regression. Kaplan-Meier analysis compared progression-free survival (PFS) curves between TCLo density groups. Test characteristics of TCLo density were explored with receiver operating characteristic (ROC) curves. Results: We included 181 patients who had CBx from 2012-2015 and met inclusion criteria. The mean age of patients was 62.58 years (standard deviation [SD] 7.13) and median followup was 60.9 months (interquartile range [IQR] 23.4). A high TCLo density score (>0.05) was independently associated with time to CP (hazard ratio [HR] 4.70; 95% confidence interval [CI] 2.62-8.42; p<0.001) and GP (HR 3.85; 95% CI 1.91-7.73; p<0.001). ROC curves showed TCLo density has greater area under the curve than number of positive cores at CBx in predicting progression. Conclusions: TCLo density is able to stratify patients on AS for risk of CP and GP. With further validation, it could be added to the decision-making algorithm in AS for low-risk localized PCa.
引用
收藏
页码:250 / 255
页数:6
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