Evidence map›Paper›PMID 40806607›Full record

ReviewInternational journal of molecular sciences2025

Omics-Mediated Treatment for Advanced Prostate Cancer: Moving Towards Precision Oncology.

Yasra Fatima, Kirubel Nigusu Jobre, Enrique Gomez-Gomez, Bartosz Małkiewicz, Antonia Vlahou, Marika Mokou, Harald Mischak, Maria Frantzi, Vera Jankowski

Abstract readReview
In one paragraph

Review 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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Metabolic convergence of diabetes and prostate cancer: from dysglycemia to tumor microenvironment reprogramming.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
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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

9 authors.

Yasra FatimaDepartment of Biomarker Research, Mosaiques Diagnostics GmbH, 30659 Hannover, Germany.ORCID 0000-0001-7386-4246
Kirubel Nigusu JobreDepartment of Biomarker Research, Mosaiques Diagnostics GmbH, 30659 Hannover, Germany.ORCID 0009-0001-5548-049X
Enrique Gomez-GomezUrology Department, Reina Sofía University Hospital, Maimonides Institute of Biomedical Research of Cordoba (IMIBIC), University of Cordoba (UCO), 14004 Cordoba, Spain.ORCID 0000-0002-8753-3306
Bartosz MałkiewiczDepartment of Minimally Invasive and Robotic Urology, Centre of Excellence in Urology, Wroclaw Medical University, 213 Borowska Street, 50-556 Wroclaw, Poland.ORCID 0000-0002-5933-3753
Antonia VlahouSystems Biology Center, Biomedical Research Foundation, Academy of Athens, 115 27 Athens, Greece.ORCID 0000-0003-3284-5713
Marika MokouDepartment of Biomarker Research, Mosaiques Diagnostics GmbH, 30659 Hannover, Germany.ORCID 0000-0002-4511-1578
Harald MischakDepartment of Biomarker Research, Mosaiques Diagnostics GmbH, 30659 Hannover, Germany.ORCID 0000-0003-0323-0306
Maria FrantziDepartment of Biomarker Research, Mosaiques Diagnostics GmbH, 30659 Hannover, Germany.ORCID 0000-0003-0415-0316
Vera JankowskiInstitute for Molecular Cardiovascular Research (IMCAR), RWTH Aachen University, 52074 Aachen, Germany.ORCID 0009-0003-6416-0230

Funding

BMBF (Federal Ministry of Education and Research) ProSTRAT-AI (01DS23014)Cost-Action CA ERA-PerMed (ERA-PERMED2022-202-KidneySign)CRU 5011 445703531Deutsche Forschungsgemeinschaft´ (DFG, German Research Foundation) TRR 219; Project-ID 322900939Marie Skłodowska Curie Actions Doctoral Networks Industrial Doctorates Programme project PROMOTE 101169245: HORIZON - MSCA-2023-DN-01-01
6 · The paper itself

Abstract

Prostate cancer accounts for approximately 1.5 million new diagnoses and 400,000 deaths every year worldwide, and demographic projections indicate a near-doubling of both figures by 2040. Despite existing treatments, 10-20% of patients eventually progress to metastatic castration-resistant disease (mCRPC). The median overall survival (OS) after progression to mCPRC drops to 24 months, and efficacy drops severely after each additional line of treatment. Omics platforms have reached advanced levels and enable the acquisition of high-resolution large datasets that can provide insights into the molecular mechanisms underlying PCa pathology. Genomics, especially DDR (DNA damage response) gene alterations, detected via tissue and/or circulating tumor DNA, efficiently guides therapy in advanced prostate cancer. Given recent developments, we have performed a comprehensive literature search to cover recent research and clinical trial reports (over the last five years) that integrate omics along three converging trajectories in therapeutic development: (i) predicting response to approved agents with demonstrated survival benefits, (ii) stratifying patients to receive therapies in clinical trials, (iii) guiding drug development as part of drug repurposing frameworks. Collectively, this review is intended to serve as a comprehensive resource of recent advancements in omics-guided therapies for advanced prostate cancer, a clinical setting with existing clinical needs and poor outcomes.

Indexed as

GenomicsPrecision MedicineProstatic NeoplasmsBiomarkers, TumorHumansMaleProstatic Neoplasms, Castration-ResistantBiomarkers, Tumorbiomarker-guided therapycombination therapymulti-omicspersonalized medicineprecision oncologytherapeutic interventionstreatment response prediction

Identifiers

PMID40806607
PMCPMC12347257

What OpenQuestion holds

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Registered trials

None linked

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.