Evidence map›Paper›PMID 40723246›Full record

ArticleCancers2025

Ex Vivo Drug Sensitivity of Pleural Effusion-Derived Cells from Lung Cancer and Pleural Mesothelioma Patients Is Linked to Clinical Response.

Rita Hutyra-Gram Ötvös, Hanna Krynska, Greta Gudoityte, Marcus Skribek, Anca Oniscu, Olena Berkovska, Katharina Strauß, Jenny Zipprick, David Tamborero, Andrey Alexeyenko and 3 more

Abstract read
In one paragraph

Article in Cancers, 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. Article
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.

Rita Hutyra-Gram ÖtvösSciLifeLab, 171 21 Solna, Sweden.
Hanna KrynskaDepartment of Oncology-Pathology, Karolinska Institutet, 171 64 Solna, Sweden.ORCID 0000-0002-3759-3503
Greta GudoityteSciLifeLab, 171 21 Solna, Sweden.ORCID 0000-0003-1963-7856
Marcus SkribekDepartment of Oncology-Pathology, Karolinska Institutet, 171 64 Solna, Sweden.ORCID 0000-0001-8692-6426
Anca OniscuDepartment of Oncology-Pathology, Karolinska Institutet, 171 64 Solna, Sweden.
Olena BerkovskaSciLifeLab, 171 21 Solna, Sweden.ORCID 0000-0002-8811-0591
Katharina StraußDepartment of Oncology-Pathology, Karolinska Institutet, 171 64 Solna, Sweden.
Jenny ZipprickDepartment of Oncology-Pathology, Karolinska Institutet, 171 64 Solna, Sweden.ORCID 0009-0001-1880-3261
David TamboreroSciLifeLab, 171 21 Solna, Sweden.
Andrey AlexeyenkoSciLifeLab, 171 21 Solna, Sweden.ORCID 0000-0001-8812-6481
Annica Karin Britt GadDepartment of Oncology-Pathology, Karolinska Institutet, 171 64 Solna, Sweden.ORCID 0000-0002-1098-9129
Brinton Seashore-LudlowSciLifeLab, 171 21 Solna, Sweden.ORCID 0000-0001-8658-5967
Katalin DobraDepartment of Oncology-Pathology, Karolinska Institutet, 171 64 Solna, Sweden.ORCID 0000-0002-0207-6733

Funding

Swedish Cancer and Allergy Foundation 10970Swedish Cancer Research Funds of Radiumhemmet 221091
6 · The paper itself

Abstract

backgroundTumors of the pleura, such as metastatic lung cancer and mesothelioma, are amongst the most lethal and therapy-resistant tumors. The first manifestation of the disease is often pleural effusion, the first available material for diagnosis. The five-year survival rate is exceptionally low, around 10-20%, and only a small proportion of patients harbor mutations that allow targeted treatments. Almost all patients develop resistance to treatment, which is often palliative. There is therefore an urgent need to refine the selection of drugs and patients for personalized treatment.

methodsWe isolated and cultured cells from pleural effusions in 3D cell aggregates and compared their drug sensitivity ex vivo to the clinical response to the same chemotherapeutic agents, combined with targeted sequencing and network analysis.

resultsThe ex vivo drug response showed a positive correlation with the treatment response and survival of patients in the clinic, with a stronger link to overall survival than to progression-free survival. Cryopreserved cells showed a similar response to freshly collected cells from the clinic.

conclusionsThe findings advance the field of ex vivo screening and present an opportunity to combine strategies for functional precision medicine with comprehensive characterization of disease for improved treatment and future management of lung cancer.

Indexed as

ex vivo drug sensitivity testingfunctional precision medicinelung cancermesotheliomametastasisnetwork enrichment analysispatient survivalpersonalized medicinepleural effusiontargeted sequencing

Identifiers

PMID40723246
PMCPMC12293284

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.