Evidence map›Paper›PMID 42820048›Full record

ArticleEuropean urology open science2026

Ex Vivo Microtumor Testing to Predict Chemotherapy Responses in Patients with Bladder Cancer.

Mathijs P Scholtes, Esmee Koedoot, Lieke J Ceton, Timothy J P Sijsenaar, Marta G Montero, Caithlyn Z Roeland, Robert J van Soest, Joost Leijte, Hossein Roshani, Ruben Korthorst and 5 more

Abstract read
In one paragraph

Article in European urology open science, 2026. 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
–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

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

15 authors.

Mathijs P ScholtesDepartment of Urology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Esmee KoedootR&D, VitroScan B.V., Leiden, The Netherlands.
Lieke J CetonR&D, VitroScan B.V., Leiden, The Netherlands.
Timothy J P SijsenaarR&D, VitroScan B.V., Leiden, The Netherlands.
Marta G MonteroR&D, VitroScan B.V., Leiden, The Netherlands.
Caithlyn Z RoelandDepartment of Urology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Robert J van SoestUrology, Franciscus Gasthuis & Vlietland, Rotterdam, The Netherlands.
Joost LeijteUrology, Amphia Ziekenhuis-location Molengracht, Breda, The Netherlands.
Hossein RoshaniUrology, Haga teaching hospital, The Hague, The Netherlands.
Ruben KorthorstUrology, Medisch Spectrum Twente, Enschede, The Netherlands.
Dieudonné J van der MeerR&D, VitroScan B.V., Leiden, The Netherlands.
Geert J L H van LeendersDepartment of Pathology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Willemijn VaderR&D, VitroScan B.V., Leiden, The Netherlands.
Joost L BoormansDepartment of Urology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Tahlita C M ZuiverloonDepartment of Urology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Patients with bladder cancer (BC) may receive intravesical or systemic chemotherapy, but predictive biomarkers to guide treatment selection are lacking. Consequently, some patients receive ineffective treatment, resulting in unnecessary toxicity and an increased risk of tumor progression. Objective: To evaluate the feasibility of ex vivo micro-tumor testing for predicting chemotherapy response in patients with BC. Design setting and participants: In this prospective study, 65 patients with BC were enrolled (Institutional Review Board no. MEC-2022-0233). Tumor samples were collected during transurethral resection or radical cystectomy. BC was confirmed by uropathological review, supported by the detection of BC-associated mutations in hTERT, FGFR3, and PIK3CA. Patient-derived micro-tumors were exposed ex vivo to anticancer drugs, and responses were assessed using image-based measurements of viability and morphology. Outcome measurements and statistical analysis: The primary outcome was successful completion of ex vivo drug testing within 14 days of tissue collection. The secondary outcome was concordance between ex vivo sensitivity and clinical response to platinum-based chemotherapy. Clinical response data were available for nine patients. Results and limitations: Ex vivo drug testing was successful for 48 of 65 patients (74%), with all successful results generated within 14 days of tissue collection. Among the nine patients with evaluable clinical outcomes following platinum-based chemotherapy, ex vivo responses corresponded with observed treatment responses. The main limitations were the small clinical correlation cohort and the limited number of drugs evaluated. Conclusions: Ex vivo micro-tumor drug testing is feasible for BC within a clinically relevant timeframe. The observed correspondence between ex vivo and clinical responses to platinum-based chemotherapy supports further investigation of this approach for personalized treatment selection in BC.

Indexed as

Bladder cancerDrug sensitivity profilingEx vivoPrecision medicine

Identifiers

PMID42820048
PMCPMC13625894

What Socratic holds

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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 Socratic graph.