Evidence map›Paper›PMID 32083990›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2020

Standard Anthracycline Based Versus Docetaxel-Capecitabine in Early High Clinical and/or Genomic Risk Breast Cancer in the EORTC 10041/BIG 3-04 MINDACT Phase III Trial.

Suzette Delaloge, Martine Piccart, Emiel Rutgers, Saskia Litière, Laura J van 't Veer, Franchette van den Berkmortel, Etienne Brain, Aleksandra Dudek-Peric, Miguel Gil-Gil, Patricia Gomez and 20 more

Open access · greenAbstract readClinical Trial, Phase IIIComparative StudyMulticenter Study
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 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
0.8field-weighted citation impact, top 27% 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, 12 citations in OpenAlex.

  1. Article
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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

30 authors at 20 institutions in 9 countries.

Suzette DelalogeGustave Roussy, Villejuif, France.
Martine PiccartInstitut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Emiel RutgersNetherlands Cancer Institute, Amsterdam, the Netherlands.
Saskia LitièreEuropean Organization for Research and Treatment of Cancer, Brussels, Belgium.
Laura J van 't VeerHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA.
Franchette van den BerkmortelZuyderland Medisch Centrum, Heerlen-Geleen, the Netherlands.
Etienne BrainInstitut Curie-Hôpital Rene Huguenin, Saint-Cloud, France.
Aleksandra Dudek-PericEuropean Organization for Research and Treatment of Cancer, Brussels, Belgium.
Miguel Gil-GilInstitut Catala D'Oncologia-Institut d'Investigacio Biomedica de Bellvitge, L'Hospitalet, Barcelona, Spain.
Patricia GomezHospital General Vall D'Hebron, Barcelona, Spain.
Florentine S HilbersBreast International Group, Brussels, Belgium.
Zaman KhalilCentre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
Susan KnoxEuropa Donna-The European Breast Cancer Coalition, Milan, Italy.
Sherko KuemmelBreast Unit Kliniken Essen-Mitte, Westdeutsche Studiengruppe, Mönchengladbach, Germany.
Georg KunzSt Johannes Hospital, Dortmund, Germany.
Anne LesurInstitut de Cancérologie de Lorraine, Vandoeuvre-Les-Nancy, France.
Jean-Yves PiergaInstitut Curie-Hôpital Rene Huguenin, Saint-Cloud, France.
Peter RavdinThe University of Texas Health Sciences Center, San Antonio, TX.
Isabel T RubioClinica Universidad de Navarra-Site Madrid, Madrid, Spain.
Mahasti SaghatchianGustave Roussy, Villejuif, France.
Tineke J SmildeJeroen Bosch Ziekenhuis, 's-Hertogenbosch, the Netherlands.
Alastair M ThompsonBaylor University College of Medicine, Houston, TX.
Giuseppe VialeUniversity of Milan and European Institute of Oncology-Istituto di Ricovero e Cura a Carattere Scientifico, Milan, Italy.
Gabriele ZoppoliUniversity of Genoa and Azienda Ospedaliera Universitaria San Martino, Genova, Italy.
Peter VuylstekeCentre Hospitalier Universitaire, Université Catholique de Louvain, Namur, Belgium.
Konstantinos TryfonidisEuropean Organization for Research and Treatment of Cancer, Brussels, Belgium.
Coralie PoncetEuropean Organization for Research and Treatment of Cancer, Brussels, Belgium.
Jan BogaertsEuropean Organization for Research and Treatment of Cancer, Brussels, Belgium.
Fatima CardosoChampalimaud Clinical Center/Champalimaud Foundation, Lisbon, Portugal.
MINDACT investigators and the TRANSBIG Consortium
European Organisation for Research and Treatment of Cancer · BEInstitut Curie · FRInstitut Gustave Roussy · FRBaylor University · USBreast International Group · BEChampalimaud Foundation · PTClinica Universidad de Navarra · ESEuropa Donna · ITInstitut de Cancérologie de Lorraine · FRInstitut d'Investigació Biomédica de Bellvitge · ESInstitut Jules Bordet · BEJeroen Bosch Ziekenhuis · NLKliniken Essen-Mitte · DEOncode Institute · NLOspedale Policlinico San Martino · ITSt.-Johannes-Hospital Dortmund · DEThe University of Texas Health Science Center at San Antonio · USUCLouvain · BEUniversity Hospital of Lausanne · CHUniversity of California, San Francisco · US

Funding

Cancer Research UK 7714
6 · The paper itself

Abstract

purposeMINDACT demonstrated that 46% of patients with early breast cancer at high clinical but low genomic risk on the basis of MammaPrint may safely avoid adjuvant chemotherapy. A second random assignment (R-C) compared docetaxel-capecitabine with an anthracycline-based regimen. PATIENTS AND

methodsR-C randomly assigned patients 1:1 between standard anthracycline-based regimens, with or without taxanes (control) and experimental docetaxel 75 mg/m

resultsOf 2,832 patients, 1,301 (45%) were randomly assigned, and 97% complied with R-C assignment. In the control arm, 29.6% only received taxanes (0.5% of N0 patients). DFS events (n = 148) were much less than required (n = 422) as a result of a lower-than-expected accrual and event rate. At 5 years of median follow-up, DFS was not different between DC (n = 652) and control (n = 649; 90.7% [95% CI, 88% to 92.8%]

conclusionAlthough underpowered, this second randomization in MINDACT did not show any improvement in outcome or safety with the use of DC compared with anthracycline-based chemotherapy.

Indexed as

AdultAgedAged, 80 and overAnthracyclinesAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsCapecitabineDocetaxelFemaleHumansMiddle AgedProspective StudiesAnthracyclinesCapecitabineDocetaxel

Identifiers

PMID32083990
PMCPMC7840116
OpenAlexW3008121670

What OpenQuestion holds

Textmetadata
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.