Evidence map›Paper›PMID 40605011›Full record

ArticleJournal of experimental & clinical cancer research : CR2025

Multicenter study correlating molecular characteristics and clinical outcomes of cancer cases with patient-derived organoids.

Paloma Navarro, Tatiana P Grazioso, Arantzazu Barquín, Maria Barba, Mónica Yagüe, Carlos Millán, Irene López, Elena Sevillano, Miguel Quiralte, Paloma Fernández and 15 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

25 authors.

Paloma Navarro *Laboratory of Innovation in Oncology, Genitourinary, Gynecological and Skin Cancer Unit, HM Clara Campal Comprehensive Cancer Centre (CIOCC) MADRID. Sanchinarro HM University Hospital, HM Hospitals, Madrid, Spain.
Tatiana P Grazioso *Laboratory of Innovation in Oncology, Genitourinary, Gynecological and Skin Cancer Unit, HM Clara Campal Comprehensive Cancer Centre (CIOCC) MADRID. Sanchinarro HM University Hospital, HM Hospitals, Madrid, Spain.
Arantzazu BarquínLaboratory of Innovation in Oncology, Genitourinary, Gynecological and Skin Cancer Unit, HM Clara Campal Comprehensive Cancer Centre (CIOCC) MADRID. Sanchinarro HM University Hospital, HM Hospitals, Madrid, Spain.
Maria BarbaLaboratory of Innovation in Oncology, Genitourinary, Gynecological and Skin Cancer Unit, HM Clara Campal Comprehensive Cancer Centre (CIOCC) MADRID. Sanchinarro HM University Hospital, HM Hospitals, Madrid, Spain.
Mónica YagüeLaboratory of Innovation in Oncology, Genitourinary, Gynecological and Skin Cancer Unit, HM Clara Campal Comprehensive Cancer Centre (CIOCC) MADRID. Sanchinarro HM University Hospital, HM Hospitals, Madrid, Spain.
Carlos MillánHM Hospitals Health Research Institute, Madrid, Spain.
Irene LópezHM Hospitals Health Research Institute, Madrid, Spain.
Elena SevillanoLaboratory of Innovation in Oncology, Genitourinary, Gynecological and Skin Cancer Unit, HM Clara Campal Comprehensive Cancer Centre (CIOCC) MADRID. Sanchinarro HM University Hospital, HM Hospitals, Madrid, Spain.
Miguel QuiralteLaboratory of Innovation in Oncology, Genitourinary, Gynecological and Skin Cancer Unit, HM Clara Campal Comprehensive Cancer Centre (CIOCC) MADRID. Sanchinarro HM University Hospital, HM Hospitals, Madrid, Spain.
Paloma FernándezInstitute of Applied Molecular Medicine (IMMA), Department of Basic Medical Sciences, Facultad de Medicina, Universidad San Pablo CEU, CEU Universities, Urbanización Montepríncipe, Madrid, Spain.
Diego LosadaLaboratory of Innovation in Oncology, Genitourinary, Gynecological and Skin Cancer Unit, HM Clara Campal Comprehensive Cancer Centre (CIOCC) MADRID. Sanchinarro HM University Hospital, HM Hospitals, Madrid, Spain.
Eduardo CaleirasHistopathology Core Unit, Spanish National Cancer Center (CNIO), Madrid, Spain.
Julia CalzasMedical Oncology Department, Fuenlabrada University Hospital, Madrid, Spain.
Beatriz JiménezHM Hospitals Health Research Institute, Madrid, Spain.
Sergio Ruiz-LlorenteLaboratory of Innovation in Oncology, Genitourinary, Gynecological and Skin Cancer Unit, HM Clara Campal Comprehensive Cancer Centre (CIOCC) MADRID. Sanchinarro HM University Hospital, HM Hospitals, Madrid, Spain.
Juan JustoHM Faculty of Health Sciences, Camilo José Cela University, Madrid, Spain.
Félix GuerreroDepartment of Urology, HM Hospitales, Kidney Division, Madrid, Spain.
Vital HeviaDepartment of Urology, HM Hospitales, Kidney Division, Madrid, Spain.
Raquel MartínDepartment of Pathology, Therapeutic Target Laboratory, Hospital Universitario HM Sanchinarro, Madrid, Spain.
Francisco José Pérez-RodriguezDepartment of Pathology, Therapeutic Target Laboratory, Hospital Universitario HM Sanchinarro, Madrid, Spain.
Julia TejerinaHospital Universitario San Jorge, Huesca, Spain.
Mario PrietoDepartment of Pathology, Therapeutic Target Laboratory, Hospital Universitario HM Sanchinarro, Madrid, Spain.
Paula ComuneVivía Biotech, Madrid, Spain.
Juan Francisco Rodriguez-MorenoLaboratory of Innovation in Oncology, Genitourinary, Gynecological and Skin Cancer Unit, HM Clara Campal Comprehensive Cancer Centre (CIOCC) MADRID. Sanchinarro HM University Hospital, HM Hospitals, Madrid, Spain.
Jesús García-DonásLaboratory of Innovation in Oncology, Genitourinary, Gynecological and Skin Cancer Unit, HM Clara Campal Comprehensive Cancer Centre (CIOCC) MADRID. Sanchinarro HM University Hospital, HM Hospitals, Madrid, Spain. jgarciadonas@hmhospitales.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background3D-spatial interaction between cancer cells influences tumor behavior, making it essential to replicate tumor structures for predicting patient outcomes.

methodsWe collected data from three multicenter prospective studies to evaluate the ability to establish Patient-Derived Organoids (PDOs) from different biological samples and timepoints, correlating their characteristics and drug sensitivity with clinical outcomes.

resultsFrom 184 patients (17 tumor types), 249 samples were collected: 149 (59.8%) from tumor tissue, 61 (24.5%) from peritoneal fluids, 39 (15.7%) from peripheral blood. Success rates for PDO establishment were 39.5%, 34.4%, and 25.6%, respectively. PDOs reproduced pathological and immunohistochemical patterns of source tumors, with pathogenic variants confirmed in 84% (21/25). In a series of 13 baseline and sequential PDOs from 9 patients undergoing treatment, responses to therapy mirrored patient responses during therapy.

conclusionsPDOs preserve tumor features, reflect disease progression, and predict treatment responses, providing valuable models to complement molecular testing in precision medicine.

Indexed as

NeoplasmsOrganoidsAdultAgedFemaleHumansMaleMiddle AgedProspective StudiesTreatment OutcomeDrug screeningPatient-derived organoidsPrecision Medicine

Identifiers

PMID40605011
PMCPMC12220348

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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.