Determining Clinically Based Factors Associated With Reclassification in the Pre-MRI Era using a Large Prospective Active Surveillance Cohort.


Journal

Urology
ISSN: 1527-9995
Titre abrégé: Urology
Pays: United States
ID NLM: 0366151

Informations de publication

Date de publication:
04 2020
Historique:
received: 28 08 2019
revised: 05 11 2019
accepted: 12 11 2019
pubmed: 4 1 2020
medline: 13 1 2022
entrez: 4 1 2020
Statut: ppublish

Résumé

To report biopsy-related and oncologic outcomes in a large prospective active surveillance cohort that was initiated in the premagnetic resonance imaging era and to additionally identify clinical factors associated with disease reclassification in order to inform future studies designed to improve enrollment and follow-up on active surveillance. Patients were prospectively enrolled at a single institution from 2006 to 2014 and followed until 2016. Men with Gleason 6 or 7 disease were eligible, and those with >6 months follow-up were included in the analysis. Patients were risk stratified based on clinical/pathologic criteria, including based on a combination of baseline and confirmatory biopsy tumor characteristics. Reclassification-free survival, based on tumor volume increase or Gleason score increase, was analyzed using multivariable Cox proportional hazards models. Of 825 enrolled patients, 682 met inclusion criteria. Median follow-up was 40 months (range 6.6-126.8). Disease was reclassified in 249 (36.5%), and 157 (23.0%) underwent treatment. A single positive core with a negative confirmatory biopsy was significantly associated with time to reclassification (median not met vs 43 months, log rank test P <.001). Composite tumor length, defined as the combined tumor length between baseline and confirmatory biopsies, was associated with shorter Gleason upgrade-free survival (hazard ratio 1.24, 95% confidence interval 1.11-1.40, P <.001) in multivariable analysis. Baseline stratification using clinical factors including tumor length may refine risk stratification and offer the foundation on which new systems that incorporate modalities such as magnetic resonance imaging may be based.

Identifiants

pubmed: 31899230
pii: S0090-4295(19)31134-3
doi: 10.1016/j.urology.2019.11.041
pmc: PMC7141963
mid: NIHMS1556242
pii:
doi:

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

91-97

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA140388
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

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Auteurs

Justin R Gregg (JR)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX. Electronic address: jrgregg@mdanderson.org.

John W Davis (JW)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Chad Reichard (C)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Xuemei Wang (X)

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX.

Mary Achim (M)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Brian F Chapin (BF)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Louis Pisters (L)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Curtis Pettaway (C)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.

John F Ward (JF)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Seungtaek Choi (S)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Quynh-Nhu Nguyen (QN)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Deborah Kuban (D)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Richard Babaian (R)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Patricia Troncoso (P)

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Lydia T Madsen (LT)

Department of Acute and Continuing Care, University of Texas Health Cizik School of Nursing, Houston, TX.

Christopher Logothetis (C)

Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Jeri Kim (J)

Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX; Affiliation change since completion of this work: Merck & Co., Inc., Kenilworth, NJ.

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Classifications MeSH