Table of Contents Table of Contents
Previous Page  329 476 Next Page
Information
Show Menu
Previous Page 329 476 Next Page
Page Background

Brief Correspondence

Quantified Clinical Risk Change as an End Point During Prostate

Cancer Active Surveillance

Michael S. Leapman

a , * ,

Niloufar Ameli

a ,

Matthew R. Cooperberg

a , b ,

Carissa Chu

a ,

Ahmed Hussein

c

[2_TD$DIFF]

,

Katsuto Shinohara

a ,

Peter R. Carroll

a

a

Department of Urology, Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA;

b

Epidemiology and Biostatistics,

Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA;

[3_TD$DIFF]

c

Department of Urology, Cairo University, Egypt

For men with favorable-risk prostate cancer (PCa) managed

with active surveillance (AS), firm end points have not been

prospectively evaluated. As a result, definitive intervention is

often undertaken in the setting of changes in biopsy grade,

prostate-specific antigen (PSA), tumor volume estimates, or

personal preference

[1]

. While periodic monitoring of such

clinical characteristics offers numerous opportunities for risk

appraisal, it is unclear whether changes in individual

parameters offer equal value in informing the necessity of

treatment. Furthermore, it is unknown if changes inmultiple

relevant characteristics may serve as an improved end point

for men managed with surveillance. Consequently, we

E U R O P E A N U R O L O G Y 7 2 ( 2 0 1 7 ) 3 2 9 – 3 3 2

ava ilable at

www.sciencedirect.com

journal homepage:

www.eu ropeanurology.com

Article info

Article history:

Accepted April 20, 2016

Associate Editor:

Giacomo Novara

Keywords:

Prostate cancer

Active surveillance

End point

CAPRA

Abstract

For men with low-stage prostate cancer (PCa) managed with active surveillance (AS),

clinical thresholds for intervention have not been definitively established. We aimed to

evaluate whether the magnitude of quantitative risk change may serve as a refined end

point. We identified 735 men managed with AS at our institution who received a

minimum of two biopsies and who were followed for a median of 52 mo. We described

the relative changes in the Cancer of the Prostate Risk Assessment (CAPRA) score from

diagnosis to last follow-up and evaluated the proportion of patients experiencing

changes in constituent clinical variables. Among patients treated with radical prosta-

tectomy (RP), the association between change in CAPRA score and the occurrence of

adverse pathology (pT3a or higher and/or primary Gleason pattern 4) was assessed

using logistic regression models. Among patients ultimately treated with RP (

n

= 196),

unit increases in CAPRA score from diagnosis were associated with the occurrence of

adverse pathology (odds ratio: 1.60; 95% confidence interval, 1.25–2.04;

p

<

[4_TD$DIFF]

0.01). On

this basis, disease reclassification should be regarded from the vantage of multiple

parameters.

Patient summary:

In this study of men with favorable-risk prostate cancer on active

surveillance, we evaluated the change in risk status from initial diagnosis to last biopsy

using a readily tabulated clinical instrument. Unit change in the Cancer of the Prostate

Risk Assessment (CAPRA) score was associated with increasing risk of adverse patho-

logic findings at delayed prostatectomy. This framework may be useful to stratify men

based on the degree of clinical change from baseline over time.

#

2016 European Association of Urology. Published by Elsevier B.V. All rights reserved.

* Corresponding author. 550 16th Street, UCSF Box 1695, San Francisco, CA 94143-1695, USA.

Tel. +1 415 353 9779; Fax: +1 415 353 9932.

E-mail address:

michael.leapman@ucsf.edu

(M.S. Leapman).

http://dx.doi.org/10.1016/j.eururo.2016.04.021

0302-2838/

#

2016 European Association of Urology. Published by Elsevier B.V. All rights reserved.