Evidence map›Paper›PMID 40565112›Full record

ArticleInternational journal of molecular sciences2025

Personalized High-Resolution Genetic Diagnostics of Prostate Adenocarcinoma Guided by Multiparametric Magnetic Resonance Imaging: Results of a Pilot Study.

Jacek Wilkosz, Dariusz Wojciech Sobieraj, Tadeusz Kałużewski, Jakub Kaczmarek, Jarosław Szwalski, Michał Bednarek, Agnieszka Morel, Żaneta Kasprzyk, Łukasz Kępczyński, Jordan Sałamunia and 2 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

12 authors.

Jacek WilkoszSecond Department of Urology, Medical University of Lodz, 93-513 Lodz, Poland.ORCID 0000-0003-4243-220X
Dariusz Wojciech SobierajDepartment of Urology and Urological Oncology, John Paul II Podkarpackie Province Hospital in Krosno, 38-400 Krosno, Poland.
Tadeusz KałużewskiDepartment of Genetics, Polish Mother's Memorial Hospital Research Institute, 93-338 Lodz, Poland.
Jakub KaczmarekGeneral Surgery Department-Endoscopy Unit and One-Day Surgery Department (Urology), Bonifraters' Medical Center, 93-378 Lodz, Poland.
Jarosław SzwalskiCYTOPATH S.A., Histopathological Laboratory, 90-552 Lodz, Poland.
Michał BednarekLaboratory of Medical Genetics, R&D Division, GENOS Sp. z o.o., 91-033 Lodz, Poland.
Agnieszka MorelLaboratory of Medical Genetics, R&D Division, GENOS Sp. z o.o., 91-033 Lodz, Poland.
Żaneta KasprzykLaboratory of Medical Genetics, R&D Division, GENOS Sp. z o.o., 91-033 Lodz, Poland.
Łukasz KępczyńskiDepartment of Genetics, Polish Mother's Memorial Hospital Research Institute, 93-338 Lodz, Poland.ORCID 0000-0002-2882-5448
Jordan SałamuniaLaboratory of Medical Genetics, R&D Division, GENOS Sp. z o.o., 91-033 Lodz, Poland.
Agnieszka GachDepartment of Genetics, Polish Mother's Memorial Hospital Research Institute, 93-338 Lodz, Poland.
Bogdan KałużewskiLaboratory of Medical Genetics, R&D Division, GENOS Sp. z o.o., 91-033 Lodz, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The upcoming wave of personalized medicine, driven by genomic diagnostics and artificial intelligence, demands clearly defined pre-laboratory and laboratory procedures to ensure the acquisition of DNA and RNA of sufficient quantity and quality. In prostate cancer oncogenetics, diagnostic and prognostic assessments increasingly rely on personalized approaches, including Comprehensive Genomic Profiling (CGP). In this pilot study, we aimed to establish optimal pre-analytical and analytical conditions for selected genetic diagnostic methods using tissue samples acquired through multiparametric MRI-guided biopsy. Tissue specimens from thirteen patients were processed for DNA isolation, fluorescence in situ hybridization (FISH), and next-generation sequencing (NGS). Comparative analyses were performed on DNA derived from both fresh and formalin-fixed, paraffin-embedded (FFPE) samples. Sequencing quality metrics demonstrated markedly superior performance in fresh tissue compared to FFPE. These results highlight the importance of standardized tissue collection and processing protocols to enable reliable molecular diagnostics in prostate cancer. Our findings support the feasibility of integrating high-quality genomic testing into routine biopsy workflows and emphasize the need for further large-scale validation.

Indexed as

AdenocarcinomaMultiparametric Magnetic Resonance ImagingPrecision MedicineProstatic NeoplasmsAgedHigh-Throughput Nucleotide SequencingHumansIn Situ Hybridization, FluorescenceMaleMiddle AgedPilot Projectsmolecular profilingMRI-guided biopsynext-generation sequencingpersonalized oncologyprostate cancer

Identifiers

PMID40565112
PMCPMC12193322

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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.