Evidence map›Paper›PMID 35267560›Full record

ArticleCancers2022

Functional Ex Vivo Tissue-Based Chemotherapy Sensitivity Testing for Breast Cancer.

Marjolijn M Ladan, Titia G Meijer, Nicole S Verkaik, Zofia M Komar, Carolien H M van Deurzen, Michael A den Bakker, Roland Kanaar, Dik C van Gent, Agnes Jager

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 34% of its field
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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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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 at 3 institutions in 1 country.

Marjolijn M LadanDepartment of Molecular Genetics, Erasmus MC Cancer Institute, University Medical Center Rotterdam, 3000 CA Rotterdam, The Netherlands.
Titia G MeijerDepartment of Molecular Genetics, Erasmus MC Cancer Institute, University Medical Center Rotterdam, 3000 CA Rotterdam, The Netherlands.ORCID 0000-0002-2235-6345
Nicole S VerkaikDepartment of Molecular Genetics, Erasmus MC Cancer Institute, University Medical Center Rotterdam, 3000 CA Rotterdam, The Netherlands.
Zofia M KomarDepartment of Molecular Genetics, Erasmus MC Cancer Institute, University Medical Center Rotterdam, 3000 CA Rotterdam, The Netherlands.
Carolien H M van DeurzenDepartment of Pathology, Erasmus MC Cancer Institute, 3000 CA Rotterdam, The Netherlands.
Michael A den BakkerDepartment of Pathology, Maasstad Ziekenhuis, 3007 AC Rotterdam, The Netherlands.
Roland KanaarDepartment of Molecular Genetics, Erasmus MC Cancer Institute, University Medical Center Rotterdam, 3000 CA Rotterdam, The Netherlands.
Dik C van GentDepartment of Molecular Genetics, Erasmus MC Cancer Institute, University Medical Center Rotterdam, 3000 CA Rotterdam, The Netherlands.ORCID 0000-0003-1473-8148
Agnes JagerDepartment of Medical Oncology, Erasmus MC Cancer Institute, 3000 CA Rotterdam, The Netherlands.
Erasmus MC · NLErasmus MC Cancer Institute · NLMaasstad Ziekenhuis · NL

Funding

Dutch Cancer Society EMCR 2008-4045Dutch Cancer Society EMCR 2014-7048Oncode Institute
6 · The paper itself

Abstract

Background chemotherapy is part of most breast cancer (BC) treatment schedules. However, a substantial fraction of BC tumors does not respond to the treatment. Unfortunately, no standard biomarkers exist for response prediction. Therefore, we aim to develop ex vivo sensitivity assays for two types of commonly used cytostatics (i.e., platinum derivates and taxanes) on organotypic BC tissue slices.

methodsEx vivo cisplatin sensitivity assays were established using organotypic tissue slices derived from the surgical resection material of 13 primary BCs and 20 fresh histological biopsies obtained from various metastatic sites. Furthermore, tissue slices of 10 primary BCs were used to establish a docetaxel ex vivo sensitivity assay.

resultsCisplatin sensitivity was assessed by tissue morphology, proliferation and apoptosis, while the relative increase in the mitotic index was discriminative for docetaxel sensitivity. Based on these read-outs, a scoring system was proposed to discriminate sensitive from resistant tumors for each cytostatic. We successful completed the cisplatin sensitivity assay on 12/16 (75%) biopsies as well.

conclusionsWe developed an ex vivo cisplatin and docetaxel assay on BC slices. We also adapted the assay for biopsy-sized specimens as the next step towards the correlation of ex vivo test results and in vivo responses.

Indexed as

breast cancerchemotherapy sensitivity testingcisplatindocetaxelex vivofunctional assay

Identifiers

PMID35267560
PMCPMC8909506
OpenAlexW4214737249

What OpenQuestion 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 OpenQuestion graph.