Evidence map›Paper›PMID 34931468›Full record

ArticleCancer reports (Hoboken, N.J.)2022

Unified model involving genomics, magnetic resonance imaging and prostate-specific antigen density outperforms individual co-variables at predicting biopsy upgrading in patients on active surveillance for low risk prostate cancer.

Alp Tuna Beksac, Parita Ratnani, Zachary Dovey, Sneha Parekh, Ugo Falagario, Reza Roshandel, Stanislaw Sobotka, Deepshikha Kewlani, Avery Davis, Rachel Weil and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 1 institution in 1 country.

Alp Tuna BeksacDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.
Parita RatnaniDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.
Zachary DoveyDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.ORCID 0000-0002-2231-8429
Sneha ParekhDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.
Ugo FalagarioDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.ORCID 0000-0002-1152-3005
Reza RoshandelDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.ORCID 0000-0001-6342-2989
Stanislaw SobotkaDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.
Deepshikha KewlaniDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.
Avery DavisDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.
Rachel WeilDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.
Hafis BashorunDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.
Ivan JamborDepartment of Radiology, Icahn School of Medicine at Mount Sinai, New York, USA.
Sara LewisDepartment of Radiology, Icahn School of Medicine at Mount Sinai, New York, USA.
Kenneth HainesDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, USA.
Ashutosh K TewariDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, USA.
Icahn School of Medicine at Mount Sinai · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundActive surveillance (AS) is the reference standard treatment for the management of low risk prostate cancer (PCa). Accurate assessment of tumor aggressiveness guides recruitment to AS programs to avoid conservative treatment of intermediate and higher risk patients. Nevertheless, underestimating the disease risk may occur in some patients recruited, with biopsy upgrading and the concomitant potential for delayed treatment.

aimTo evaluate the accuracy of mpMRI and GPS for the prediction of biopsy upgrading during active surveillance (AS) management of prostate cancer (PCa).

methodA retrospective analysis was performed on 144 patients recruited to AS from October 2013 to December 2020. Median follow was 4.8 (IQR 3.6, 6.3) years. Upgrading was defined as upgrading to biopsy grade group ≥2 on follow up biopsies. Cox proportional hazard regression was used to investigate the effect of PSA density (PSAD), baseline Prostate Imaging-Reporting and Data System (PI-RADS) v2.1 score and GPS on upgrading. Time-to-event outcome, defined as upgrading, was estimated using the Kaplan-Meier method with log-rank test.

resultsOverall rate of upgrading was 31.9% (n = 46). PSAD was higher in the patients who were upgraded (0.12 vs. 0.08 ng/ml

conclusionIn this study PSAD has higher accuracy over baseline PI-RADS score and GPS score for the prediction of PCa upgrading during AS. However, combined use of PSAD, GPS and PI-RADS Score yielded the highest predictive ability with a concordance index of 0.71.

Indexed as

Prostate-Specific AntigenProstatic NeoplasmsGenomicsHumansImage-Guided BiopsyMagnetic Resonance ImagingMaleRetrospective StudiesWatchful WaitingProstate-Specific Antigenactive surveillancebiomarkergenomic prostate scoremultiparametric MRIoncotypeprostate cancerPSA density

Identifiers

PMID34931468
PMCPMC8955055
OpenAlexW4200546355

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Registered trials

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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.