Evidence map›Paper›PMID 32719399›Full record

ArticleCommunications biology2020

Controlling technical variation amongst 6693 patient microarrays of the randomized MINDACT trial.

Laurent Jacob, Anke Witteveen, Inès Beumer, Leonie Delahaye, Diederik Wehkamp, Jeroen van den Akker, Mireille Snel, Bob Chan, Arno Floore, Niels Bakx and 10 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Transcriptomic Insights into Lobular Breast Cancer Biology and Patient Outcomes: Analysis of the MINDACT Clinical Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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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

20 authors at 9 institutions in 7 countries.

Laurent JacobUniversité de Lyon, Université Lyon 1, CNRS, Laboratoire de Biométrie et Biologie Évolutive UMR 5558, Villeurbanne, France.ORCID http://orcid.org/0000-0002-7826-2719
Anke WitteveenAgendia NV/Agendia Inc, Amsterdam, The Netherlands.
Inès BeumerAgendia NV/Agendia Inc, Amsterdam, The Netherlands.
Leonie DelahayeAgendia NV/Agendia Inc, Amsterdam, The Netherlands.
Diederik WehkampAgendia NV/Agendia Inc, Amsterdam, The Netherlands.
Jeroen van den AkkerAgendia NV/Agendia Inc, Amsterdam, The Netherlands.
Mireille SnelAgendia NV/Agendia Inc, Amsterdam, The Netherlands.
Bob ChanAgendia NV/Agendia Inc, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-8616-9565
Arno FlooreAgendia NV/Agendia Inc, Amsterdam, The Netherlands.
Niels BakxAgendia NV/Agendia Inc, Amsterdam, The Netherlands.
Guido BrinkAgendia NV/Agendia Inc, Amsterdam, The Netherlands.
Coralie PoncetEORTC, Brussels, Belgium.
Jan BogaertsEORTC, Brussels, Belgium.
Mauro DelorenziUniversity Lausanne, Lausanne, Switzerland.ORCID http://orcid.org/0000-0001-7631-3263
Martine PiccartInstitute Jules Bordet, Brussels, Belgium.
Emiel RutgersNetherlands Cancer Institute, Amsterdam, The Netherlands.
Fatima CardosoChampalimaud, Lisbon, Portugal.ORCID http://orcid.org/0000-0002-6692-2249
Terence SpeedWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-5403-7998
Laura van 't VeerAgendia NV/Agendia Inc, Amsterdam, The Netherlands. Laura.Vantveer@ucsf.edu.ORCID http://orcid.org/0000-0002-9838-8298
Annuska GlasAgendia NV/Agendia Inc, Amsterdam, The Netherlands. annuska.glas@agendia.com.ORCID http://orcid.org/0000-0002-0775-138X
Agendia (Netherlands) · NLEuropean Organisation for Research and Treatment of Cancer · BEChampalimaud Foundation · PTInstitut Jules Bordet · BESIB Swiss Institute of Bioinformatics · CHThe Netherlands Cancer Institute · NLUCSF Helen Diller Family Comprehensive Cancer Center · USUniversité Claude Bernard Lyon 1 · FRWalter and Eliza Hall Institute of Medical Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene expression data obtained in large studies hold great promises for discovering disease signatures or subtypes through data analysis. It is also prone to technical variation, whose removal is essential to avoid spurious discoveries. Because this variation is not always known and can be confounded with biological signals, its removal is a challenging task. Here we provide a step-wise procedure and comprehensive analysis of the MINDACT microarray dataset. The MINDACT trial enrolled 6693 breast cancer patients and prospectively validated the gene expression signature MammaPrint for outcome prediction. The study also yielded a full-transcriptome microarray for each tumor. We show for the first time in such a large dataset how technical variation can be removed while retaining expected biological signals. Because of its unprecedented size, we hope the resulting adjusted dataset will be an invaluable tool to discover or test gene expression signatures and to advance our understanding of breast cancer.

Indexed as

PrognosisAdultAgedBiomarkers, TumorBreast NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedNeoplasm ProteinsProtein Array AnalysisRandomized Controlled Trials as TopicTranscriptomeBiomarkers, TumorNeoplasm Proteins

Identifiers

PMID32719399
PMCPMC7385160
OpenAlexW3044611194

What OpenQuestion 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 OpenQuestion graph.