Evidence map›Paper›PMID 31612251›Full record

ArticleWorld journal of urology2020

Active surveillance eligibility of MRI-positive patients with grade group 2 prostate cancer: a pathological study.

Guillaume Ploussard, Jean-Baptiste Beauval, Marine Lesourd, Cécile Manceau, Christophe Almeras, Richard Aziza, Jean-Romain Gautier, Guillaume Loison, Daniel Portalez, Ambroise Salin and 4 more

Abstract read
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Article in World journal of urology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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

14 authors at 3 institutions in 1 country.

Guillaume PloussardDepartment of Urology, La Croix du Sud Hospital, 52, chemin de Ribaute, 31130, Quint Fonsegrives, France. g.ploussard@gmail.com.ORCID http://orcid.org/0000-0002-6004-2152
Jean-Baptiste BeauvalDepartment of Urology, La Croix du Sud Hospital, 52, chemin de Ribaute, 31130, Quint Fonsegrives, France.
Marine LesourdDepartment of Urology, Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
Cécile ManceauDepartment of Urology, Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
Christophe AlmerasDepartment of Urology, La Croix du Sud Hospital, 52, chemin de Ribaute, 31130, Quint Fonsegrives, France.
Richard AzizaDepartment of Radiology, Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
Jean-Romain GautierDepartment of Urology, La Croix du Sud Hospital, 52, chemin de Ribaute, 31130, Quint Fonsegrives, France.
Guillaume LoisonDepartment of Urology, La Croix du Sud Hospital, 52, chemin de Ribaute, 31130, Quint Fonsegrives, France.
Daniel PortalezDepartment of Radiology, Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
Ambroise SalinDepartment of Urology, La Croix du Sud Hospital, 52, chemin de Ribaute, 31130, Quint Fonsegrives, France.
Christophe TollonDepartment of Urology, La Croix du Sud Hospital, 52, chemin de Ribaute, 31130, Quint Fonsegrives, France.
Michel SouliéDepartment of Urology, CHU Toulouse, Toulouse, France.
Bernard MalavaudDepartment of Urology, Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
Mathieu RoumiguiéDepartment of Urology, Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
Lyon Genou Centre Albert Trillat · FRCentre Hospitalier Universitaire de Toulouse · FRInstitut universitaire du cancer de Toulouse Oncopole · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo assess the final pathology risk in MRI-positive grade group (GG) 2 prostate cancer (PCa) patients undergoing targeted (TB) and systematic (SB) biopsies, and thereby, the possibility of active surveillance (AS) in this population. PATIENTS AND

methodsWe included 242 consecutive men diagnosed with GG2 PCa by a combination of SB and software-based fusion TB undergoing a radical prostatectomy (RP). The primary endpoints were the pathological findings in RP specimens, including favourable disease which was defined by a pT2 and GG1-2 disease.

resultsThe rate of upgrading was 33% including 3% of GG 4-5 disease. MRI lesion size (p = 0.038) and tumor length per core (p < 0.001) were significantly lower in case of favourable pathology. Only 34.2% of not organ-confined disease was reported when only SB were positive, compared with 45.7% and 57.1% when GG2 was detected on TB only and on TB plus SB, respectively (p = 0.035). The number of positive cores on SB was significantly higher in not organ-confined disease (4.3 versus 2.9; p = 0.005). The risk of not organ-confined disease was only 20.8% in men who had a PSAD ≤ 0.20 ng/ml/gr, 1-2 positive biopsies and a maximal tumor length ≤ 6 mm per core, compared with 52.3% in men who did not fulfil all these criteria (p = 0.003).

conclusionsThis study identified clinical, imaging, and pathological factors that were significantly associated with the final pathology risk. In case of positive MRI followed by TB showing GG2, AS could be offered in patients having a PSAD ≤ 0.20, a tumor length ≤ 6 mm and 1-2 positive cores.

Indexed as

Magnetic Resonance ImagingWatchful WaitingAgedEligibility DeterminationHumansMaleMiddle AgedNeoplasm GradingProstatic NeoplasmsRisk AssessmentActive surveillanceBiopsyFusion biopsiesIntermediate riskProstate cancerRadical prostatectomyTargeted biopsies, MRI

Identifiers

PMID31612251
OpenAlexW2979788918

What OpenQuestion holds

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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.