Evidence map›Paper›PMID 31899230›Full record

Observational studyUrology2020

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

Justin R Gregg, John W Davis, Chad Reichard, Xuemei Wang, Mary Achim, Brian F Chapin, Louis Pisters, Curtis Pettaway, John F Ward, Seungtaek Choi and 7 more

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Urology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 2 institutions in 1 country.

Justin R GreggDepartment of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX. Electronic address: jrgregg@mdanderson.org.
John W DavisDepartment of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Chad ReichardDepartment of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Xuemei WangDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX.
Mary AchimDepartment of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Brian F ChapinDepartment of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Louis PistersDepartment of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Curtis PettawayDepartment of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.
John F WardDepartment of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Seungtaek ChoiDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Quynh-Nhu NguyenDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Deborah KubanDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Richard BabaianDepartment of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Patricia TroncosoDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Lydia T MadsenDepartment of Acute and Continuing Care, University of Texas Health Cizik School of Nursing, Houston, TX.
Christopher LogothetisDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Jeri KimDepartment 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.
The University of Texas MD Anderson Cancer Center · USThe University of Texas Health Science Center at Houston · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Targeting Tumor Microenvironment-Induced Therapy Resistance in Prostate Cancer Bone MetastasisP50CA140388 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI THOMPSON, TIMOTHY CHARLES · 2009 to 2022
$23.4M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA140388
6 · The paper itself

Abstract

objectiveTo 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.

methodsPatients 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.

resultsOf 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.

conclusionBaseline 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.

Indexed as

AgedBiopsyDisease ProgressionFollow-Up StudiesHumansMaleMiddle AgedNeoplasm GradingProgression-Free SurvivalProspective StudiesProstateProstatic NeoplasmsRisk AssessmentTumor BurdenWatchful Waiting

Identifiers

PMID31899230
PMCPMC7141963
OpenAlexW2997419251

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.