Evidence map›Paper›PMID 40917391›Full record

ArticleSmall science2025

Label-Free Machine Learning Prediction of Chemotherapy on Tumor Spheroids Using a Microfluidics Droplet Platform.

Caroline Parent, Hasti Honari, Tiziana Tocci, Franck Simon, Sakina Zaidi, Audric Jan, Vivian Aubert, Olivier Delattre, Hervé Isambert, Claire Wilhelm and 1 more

Abstract read
In one paragraph

Article in Small science, 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

11 authors.

Caroline ParentCNRS UMR168 Laboratoire Physique des Cellules et Cancer Institut Curie PSL Research University 26 rue d'Ulm 75 005 Paris France.ORCID https://orcid.org/0000-0003-2513-5377
Hasti HonariCNRS UMR168 Laboratoire Physique des Cellules et Cancer Institut Curie PSL Research University 26 rue d'Ulm 75 005 Paris France.ORCID https://orcid.org/0009-0005-3091-0421
Tiziana TocciCNRS UMR168 Laboratoire Physique des Cellules et Cancer Institut Curie PSL Research University 26 rue d'Ulm 75 005 Paris France.ORCID https://orcid.org/0000-0001-8103-4592
Franck SimonCNRS UMR168 Laboratoire Physique des Cellules et Cancer Institut Curie PSL Research University 26 rue d'Ulm 75 005 Paris France.ORCID https://orcid.org/0000-0002-6952-0819
Sakina ZaidiINSERM U1330 Children's Oncology Research Unit Research Center PSL Research University Institut Curie 26 rue d'Ulm 75 005 Paris France.
Audric JanUAR3750 CNRS Plateforme technologique Institut Pierre Gilles de Gennes PSL Research University 6 rue Jean Calvin 75 005 Paris France.ORCID https://orcid.org/0000-0001-5006-4190
Vivian AubertCNRS UMR168 Laboratoire Physique des Cellules et Cancer Institut Curie PSL Research University 26 rue d'Ulm 75 005 Paris France.
Olivier DelattreINSERM U1330 Children's Oncology Research Unit Research Center PSL Research University Institut Curie 26 rue d'Ulm 75 005 Paris France.ORCID https://orcid.org/0000-0002-8730-2276
Hervé IsambertCNRS UMR168 Laboratoire Physique des Cellules et Cancer Institut Curie PSL Research University 26 rue d'Ulm 75 005 Paris France.ORCID https://orcid.org/0000-0001-9638-8545
Claire WilhelmCNRS UMR168 Laboratoire Physique des Cellules et Cancer Institut Curie PSL Research University 26 rue d'Ulm 75 005 Paris France.ORCID https://orcid.org/0000-0001-7024-9627
Jean-Louis ViovyCNRS UMR168 Laboratoire Physique des Cellules et Cancer Institut Curie PSL Research University 26 rue d'Ulm 75 005 Paris France.ORCID https://orcid.org/0000-0002-8223-4040

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An integrated approach is proposed to rapidly evaluate the effects of anticancer treatments in 3D models, combining a droplet-based microfluidic platform for spheroid formation and single-spheroid chemotherapy application, label-free morphological analysis, and machine learning to assess treatment response. Morphological features of spheroids, such as size and color intensity, are extracted and selected using the multivariate information-based inductive causation algorithm, and used to train a neural network for spheroid classification into viability classes, derived from metabolic assays performed within the same platform as a benchmark. The model is tested on Ewing sarcoma cell lines and patient-derived xenograft (PDX) cells, demonstrating robust performance across datasets. It accurately predicts spheroid viability, used to generate dose-response curves and to determine half maximal inhibitory concentration (IC50) values comparable to traditional biochemical assays. Notably, a model trained on cell line spheroids successfully classifies PDX spheroids, highlighting its adaptability. Compared to convolutional neural network-based approaches, this method works with smaller training datasets and provides greater interpretability by identifying key morphological features. The droplet platform further reduces cell requirements, while single-spheroid confinement enhances classification quality. Overall, this label-free experimental and analytical platform is confirmed as a scalable, efficient, and dynamic tool for drug screening.

Indexed as

droplet microfluidicsdrug testinglabel‐freemachine learningtumor spheroids

Identifiers

PMID40917391
PMCPMC12412520

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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.