Evidence map›Paper›PMID 37923752›Full record

ArticleNature communications2023

Immunological and clinicopathological features predict HER2-positive breast cancer prognosis in the neoadjuvant NeoALTTO and CALGB 40601 randomized trials.

Mattia Rediti, Aranzazu Fernandez-Martinez, David Venet, Françoise Rothé, Katherine A Hoadley, Joel S Parker, Baljit Singh, Jordan D Campbell, Karla V Ballman, David W Hillman and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. The immunology of human breast cancer.Nature reviews. Immunology · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
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  12. BREAST CANCER: STEPS AND STUMBLES ON THE WAY TO PRECISION MEDICINE.Transactions of the American Clinical and Climatological Association · 2025
    Review
  13. Article
  14. Review
  15. 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

22 authors at 10 institutions in 4 countries.

Mattia ReditiBreast Cancer Translational Research Laboratory, Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université Libre de Bruxelles (ULB), Brussels, Belgium.ORCID 0000-0002-6713-2599
Aranzazu Fernandez-MartinezLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
David VenetBreast Cancer Translational Research Laboratory, Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université Libre de Bruxelles (ULB), Brussels, Belgium.
Françoise RothéBreast Cancer Translational Research Laboratory, Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université Libre de Bruxelles (ULB), Brussels, Belgium.
Katherine A HoadleyLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.ORCID 0000-0002-1216-477X
Joel S ParkerLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.ORCID 0000-0003-2080-6901
Baljit SinghWhite Plains Hospital, White Plains, NY, USA.
Jordan D CampbellAlliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN, USA.
Karla V BallmanAlliance Statistics and Data Management Center, Weill Cornell Medicine, New York, NY, USA.
David W HillmanAlliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0002-0519-1147
Eric P WinerYale Cancer Center, Yale School of Medicine, New Haven, CT, USA.
Sarra El-AbedBreast International Group, Brussels, Belgium.
Martine PiccartMedical Oncology Department, Institut Jules Bordet and l'Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.ORCID 0000-0001-9068-8504
Serena Di CosimoIntegrated biology platform unit, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-4666-8052
William Fraser SymmansDepartment of Pathology, University of Texas, MD Anderson Cancer Center, Houston, TX, 77030, USA.ORCID 0000-0002-1526-184X
Ian E KropYale Cancer Center, Yale School of Medicine, New Haven, CT, USA.
Roberto SalgadoDepartment of Pathology, GZA-ZNA Ziekenhuizen, Antwerp, Belgium.ORCID 0000-0002-1110-3801
Sherene LoiDivision of Research, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.ORCID 0000-0001-6137-9171
Lajos PusztaiBreast Medical Oncology, Yale Cancer Center, Yale School of Medicine, New Haven, CT, USA.ORCID 0000-0001-9632-6686
Charles M PerouLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.ORCID 0000-0001-9827-2247
Lisa A CareyDivision of Hematology-Oncology, Department of Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID 0000-0003-2388-4649
Christos SotiriouBreast Cancer Translational Research Laboratory, Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université Libre de Bruxelles (ULB), Brussels, Belgium. christos.sotiriou@hubruxelles.be.ORCID 0000-0002-5745-9977
Université Libre de Bruxelles · BEUniversity of North Carolina at Chapel Hill · USYale Cancer Center · USMayo Clinic · USPeter MacCallum Cancer Centre · AUBreast International Group · BECornell University · USFondazione IRCCS Istituto Nazionale dei Tumori · ITThe University of Texas MD Anderson Cancer Center · USWhite Plains Hospital · US

Funding

Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Statistics CoreU10CA180882 · NCI · MAYO CLINIC ROCHESTER · PI Sumithra Jay Mandrekar · 2014 to 2026
$115.0M
Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Stephanie Engel · 2001 to 2026
$36.3M
THE ALLIANCE NCTN BIOREPOSITORY AND BIOSPECIMEN RESOURCEU24CA196171 · NCI · WASHINGTON UNIVERSITY · PI Mine Cicek, Wendy Frankel · 2015 to 2026
$35.0M
NCTN Lead Academic Participating Site at Dana-Farber/Partners Cancer CareUG1CA233180 · NCI · DANA-FARBER CANCER INST · PI Harold John Burstein · 2019 to 2026
$8.6M
Yale Cancer Center NCTN LAPSUG1CA233337 · NCI · YALE UNIVERSITY · PI ANNE C CHIANG · 2019 to 2026
$6.0M
Optimizing prognostic and predictive algorithms using residual disease (RD) genomic biomarkers in HER2+ and TNBCR01CA229409 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LISA A CAREY, CHARLES M PEROU · 2019 to 2026
$4.0M
UNC Lead Academic Participating SiteUG1CA233373 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CAREY, LISA A, DEES, ELIZABETH CLAIRE · 2019 to 2025
$3.5M
NCATS NIH HHS UL1 TR001863NCI NIH HHS R01 CA229409NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180882NCI NIH HHS U24 CA196171NCI NIH HHS UG1 CA233180NCI NIH HHS UG1 CA233337NCI NIH HHS UG1 CA233373NIEHS NIH HHS P30 ES010126
6 · The paper itself

Abstract

The identification of prognostic markers in patients receiving neoadjuvant therapy is crucial for treatment optimization in HER2-positive breast cancer, with the immune microenvironment being a key factor. Here, we investigate the complexity of B and T cell receptor (BCR and TCR) repertoires in the context of two phase III trials, NeoALTTO and CALGB 40601, evaluating neoadjuvant paclitaxel with trastuzumab and/or lapatinib in women with HER2-positive breast cancer. BCR features, particularly the number of reads and clones, evenness and Gini index, are heterogeneous according to hormone receptor status and PAM50 subtypes. Moreover, BCR measures describing clonal expansion, namely evenness and Gini index, are independent prognostic factors. We present a model developed in NeoALTTO and validated in CALGB 40601 that can predict event-free survival (EFS) by integrating hormone receptor and clinical nodal status, breast pathological complete response (pCR), stromal tumor-infiltrating lymphocyte levels (%) and BCR repertoire evenness. A prognostic score derived from the model and including those variables, HER2-EveNT, allows the identification of patients with 5-year EFS > 90%, and, in those not achieving pCR, of a subgroup of immune-enriched tumors with an excellent outcome despite residual disease.

Indexed as

Breast NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsClinical Trials, Phase III as TopicErb-b2 Receptor Tyrosine KinasesFemaleHormonesHumansNeoadjuvant TherapyRandomized Controlled Trials as TopicTrastuzumabTreatment OutcomeTumor MicroenvironmentErb-b2 Receptor Tyrosine KinasesHormonesTrastuzumab

Identifiers

PMID37923752
PMCPMC10624889
OpenAlexW4388290806

What OpenQuestion holds

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LicenceCC BY
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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.