Evidence map›Paper›PMID 30899086›Full record

Trial reportBritish journal of cancer2019

Molecular apocrine tumours in EORTC 10994/BIG 1-00 phase III study: pathological response after neoadjuvant chemotherapy and clinical outcomes.

Hervé Bonnefoi, Gaetan MacGrogan, Coralie Poncet, Richard Iggo, Fanny Pommeret, Thomas Grellety, Denis Larsimont, Véronique Bécette, Olivier Kerdraon, Frédéric Bibeau and 9 more

Abstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in British journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Observational
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Triple-negative breast lobular carcinoma: a luminal androgen receptor carcinoma with specific ESRRA mutations.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  9. 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

19 authors.

Hervé BonnefoiDepartment of Medical Oncology, Institut Bergonié Unicancer, University of Bordeaux, INSERM U1218, INSERM CIC1401, Bordeaux, France. h.bonnefoi@bordeaux.unicancer.fr.
Gaetan MacGroganDepartment of BioPathology, Institut Bergonié Unicancer, INSERM U1218, Bordeaux, France.
Coralie PoncetEuropean Organisation for Research and Treatment of Cancer EORTC) Headquarters, Brussels, Belgium.
Richard IggoInstitut Bergonié Unicancer, INSERM U1218, Bordeaux, France.
Fanny PommeretDepartment of Medical Oncology, Institut Bergonié Unicancer, University of Bordeaux, INSERM U1218, INSERM CIC1401, Bordeaux, France.
Thomas GrelletyDepartment of Medical Oncology, Institut Bergonié Unicancer, University of Bordeaux, INSERM U1218, INSERM CIC1401, Bordeaux, France.
Denis LarsimontDepartment of Pathology, Institut Jules Bordet, Brussels, Belgium.
Véronique BécetteDepartment of Pathology, Institut Curie-Hôpital René Huguenin, Saint-Cloud, France.
Olivier KerdraonDepartment of Pathology, Centre René Gauducheau, Institut de Cancérologie de l'Ouest, Nantes, France.
Frédéric BibeauDepartment of Pathology, Institut de Cancérologie de Montpellier (ICM), Montpellier, France.
Jean-Pierre GhnassiaDepartment of Pathology, Centre Paul Strauss, Strasbourg, France.
Jean-Michel PicquenotDepartment of Pathology, Centre Henri Becquerel, Rouen, France.
Jeremy ThomasDepartment of Pathology, Edinburgh Cancer Centre, University of Edinburgh, Edinburgh, United Kingdom.
Jean-Christophe TilleDepartment of Pathologie, Hôpitaux Universitaires de Genève (HUG), Geneva, Switzerland.
Leen SlaetsEuropean Organisation for Research and Treatment of Cancer EORTC) Headquarters, Brussels, Belgium.
Alexandre BodmerSwiss Group for Clinical Cancer Research (SAKK), Bern, Switzerland.
Jonas BerghSwedish Breast Cancer Group (SweBCG), Stockholm, Sweden.
David CameronAnglo-Celtic Cooperative Oncology Group (ACCOG), Edinburgh, United Kingdom.
EORTC 10994/BIG 1-00 study investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe explored, within the EORTC10994 study, the outcomes for patients with molecular apocrine (MA) breast cancer, and defined immunohistochemistry (IHC) as androgen-receptor (AR) positive, oestrogen (ER) and progesterone (PR) negative. We also assessed the concordance between IHC and gene expression arrays (GEA) in the identification of MA cancers.

methodsCentrally assessed biopsies for AR, ER, PR, HER2 and Ki67 by IHC were classified into six subtypes: MA, triple-negative (TN) basal-like, luminal A, luminal B HER2 negative, luminal B HER2 positive and "other". The two main objectives were the pCR rates and survival outcomes in the overall MA subtype (and further divided by HER2 status) and the remaining five subtypes.

resultsIHC subtyping was obtained in 846 eligible patients. Ninety-three (11%) tumours were classified as the MA subtype. Both IHC and GEA data were available for 64 patients. In this subset, IHC concordance was 88.3% in identifying MA tumours compared with GEA. Within the MA subtype, pCR was observed in 33.3% of the patients (95% CI: 29.4-43.9) and the 5-year recurrence-free interval was 59.2% (95% CI: 48.2-68.6). Patients with MA and TN basal-like tumours have lower survival outcomes.

conclusionsIrrespective of their HER2 status, the prognosis for MA tumours remains poor and adjuvant trials evaluating anti-androgens should be considered.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsChemotherapy, AdjuvantDisease-Free SurvivalErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFemaleGene Expression ProfilingHumansImmunohistochemistryReceptors, AndrogenReceptors, EstrogenReceptors, ProgesteroneSurvival RateTreatment OutcomeAR protein, humanEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsReceptors, AndrogenReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID30899086
PMCPMC6734658

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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.