Evidence map›Paper›PMID 41077599›Full record

ArticleEJNMMI reports2025

Characterization of suspicious prostate lesions at multiparametric MRI with dynamic

Daniel Parrott, Qing Yuan, Daniella Pinho, Yin Xi, Daniel N Costa, Alberto Diaz De Leon, Marianna Dakanali, Xiankai Sun, Orhan K Oz, Spencer Bowen and 3 more

Abstract read
In one paragraph

Article in EJNMMI reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Daniel ParrottUniversity of Texas Southwestern Medical Center, Dallas, USA. Daniel.parrott@nyulangone.org.ORCID http://orcid.org/0000-0001-5871-3431
Qing YuanUniversity of Texas Southwestern Medical Center, Dallas, USA.
Daniella PinhoUniversity of Texas Southwestern Medical Center, Dallas, USA.
Yin XiUniversity of Texas Southwestern Medical Center, Dallas, USA.
Daniel N CostaUniversity of Texas Southwestern Medical Center, Dallas, USA.
Alberto Diaz De LeonUniversity of Texas Southwestern Medical Center, Dallas, USA.
Marianna DakanaliUniversity of Texas Southwestern Medical Center, Dallas, USA.
Xiankai SunUniversity of Texas Southwestern Medical Center, Dallas, USA.
Orhan K OzUniversity of Texas Southwestern Medical Center, Dallas, USA.
Spencer BowenUniversity of Texas Southwestern Medical Center, Dallas, USA.
Neil M RofskyUniversity of Texas Southwestern Medical Center, Dallas, USA.
Dana MathewsUniversity of Texas Southwestern Medical Center, Dallas, USA.
Ivan PedrosaUniversity of Texas Southwestern Medical Center, Dallas, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate cancer (PCa) will affect approximately 12% of US men in their lifetime and remains the 2nd most common cause of cancer-specific death. However, there is a broad spectrum of severity of PCa; some require aggressive treatment and others can "watch-and-wait". Distinction of clinically significant prostate cancer (csPCa) from indolent PCA with current imaging methods remains challenging.

objectiveThis study aims to evaluate dynamic prostate specific membrane antigen (PSMA) positron emission tomography (PET/CT) in the characterization of suspicious prostate lesions identified on multiparametric MRI (mpMRI).

methodsProspective study of biopsy-naïve patients with at least one Prostate Imaging and Reporting Data System (PI-RADS) score 5 or one PI-RADS score 4 plus a prostate specific antigen (PSA) ≥ 10 ng/mL. Dynamic PET/CT was performed for 30 min after administration of

results19 PI-RADS v2.1 ≥ 4 and 6 secondary PI-RADS v2.1 ≥ 3 lesions in 19 patients were analyzed: 4 (16.0%) grade group (GG) 0 (benign), 3 (12.0%) GG 1, 6 (24.0%) GG 2, 6 (24.0%) GG 3, and 6 (24.0%) GG ≥ 4. Significant differences in slope values were observed between clinically insignificant disease (GG 0/1) and GG 2 or higher as early as 5 min post-injection (p < 0.05). At 30 min, GG 1 had the lowest mean slope (- 0.18 ± 0.57) and GG ≥ 4 exhibited the highest mean slope (2.35 ± 2.03). Slope value/ADC ratio further improved discrimination between different GGs.

conclusionsDynamic CLINICAL IMPLICATIONS: Dynamic

Identifiers

PMID41077599
PMCPMC12515795

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