Evidence map›Paper›PMID 40072539›Full record

ArticleAbdominal radiology (New York)2025

The presence of prostate MRI-visible lesions at follow-up biopsy as a risk factor for histopathological upgrading during active surveillance.

Publio Cesar Cavalcante Viana, Paulo Victor Alves Pinto, Natally Horvat, Marcelo Araújo Queiroz, Maurício Dener Cordeiro, Rafael Ferreira Coelho, Leonardo Cardili, Jose Pontes, Giovanni Guido Cerri, William Carlos Nahas

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Article in Abdominal radiology (New York), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Publio Cesar Cavalcante VianaUniversidade de São Paulo, São Paulo, Brazil. publioviana@gmail.com.
Paulo Victor Alves PintoUniversidade de São Paulo, São Paulo, Brazil.
Natally HorvatMayo Clinic, Rochester, USA. horvat.natally@mayo.edu.
Marcelo Araújo QueirozUniversidade de São Paulo, São Paulo, Brazil.
Maurício Dener CordeiroUniversidade de São Paulo, São Paulo, Brazil.
Rafael Ferreira CoelhoUniversidade de São Paulo, São Paulo, Brazil.
Leonardo CardiliUniversidade de São Paulo, São Paulo, Brazil.
Jose PontesUniversidade de São Paulo, São Paulo, Brazil.
Giovanni Guido CerriUniversidade de São Paulo, São Paulo, Brazil.
William Carlos NahasUniversidade de São Paulo, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo prospectively determine the ability of visible lesions on multiparametric MRI (PI-RADS 4-5) and commonly used biomarkers to predict disease upgrading on rebiopsy in men with low-risk prostate cancer (PCa) enrolled in active surveillance (AS). MATERIALS AND

methodsFor this prospective study, approved by the Institutional Review Board (IRB), we selected consecutive patients with low-risk, low-grade, and localized prostate cancer (PCa) from our active surveillance (AS) program, who were enrolled between March 2014 and December 2020. Patients who had undergone previous prostate surgery, hormonal treatment, had contraindications for mpMRI, or transrectal ultrasound-guided (TRUS) biopsy were excluded from this study. All eligible patients underwent mpMRI at least 3 months after the initial biopsy, followed by MRI-targeted TRUS-guided re-biopsy within 12 months after enrollment. The mpMRI studies were evaluated by an experienced radiologist using the PI-RADS v2 classification. Statistical significance was determined by comparing the results from the MRI with the pathology data from rebiopsy.

resultsThere were 240 patients included. Overall upgrading rate was 41.2% (99/240), higher among patients classified as PIRADS 4 or 5 (77%). MRI sensitivity was 77.7% and specificity was 83.6% on re-biopsy. Visible lesion on mpMRI, PSA density and 3 + /12 positive cores at the first biopsy were good predictors of disease upgrade on rebiopsy. On our predictive model, patients with PI-RADS 4 or 5, PSA density > 0.15 ng/mL/cm

conclusionPatients in AS with PI-RADS 4 or 5 lesions, PSA density > 0.15 ng/mL/cm

Indexed as

Magnetic Resonance ImagingMultiparametric Magnetic Resonance ImagingProstatic NeoplasmsWatchful WaitingAgedHumansImage-Guided BiopsyMaleMiddle AgedNeoplasm GradingProspective StudiesProstateRisk FactorsImage-guided biopsyMagnetic resonance imagingProstatectomyProstatic neoplasmsWatchful waiting

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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.