Evidence map›Paper›PMID 28453704›Full record

ArticleAnnals of oncology : official journal of the European Society for Medical Oncology2017

Genomic characterization of HER2-positive breast cancer and response to neoadjuvant trastuzumab and chemotherapy-results from the ACOSOG Z1041 (Alliance) trial.

R Lesurf, O L Griffith, M Griffith, J Hundal, L Trani, M A Watson, R Aft, M J Ellis, D Ota, V J Suman and 7 more

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Annals of oncology : official journal of the European Society for Medical Oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 46 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 2 pooled it
3.5field-weighted citation impact, top 6% 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.

NCT00353483 recruitingnot on this map

Effect of Neoadjuvant or Adjuvant Systemic Therapy on Breast Cancers, Bone Marrow Cancer Cells, and Circulating Cancer Cells

TypeobservationalSponsorWashington University School of MedicineRan2005 to 2026Enrolled300ConditionsBreast NeoplasmsArmsPeripheral blood draw, Breast tissue collection, Bone marrow biopsy
NCT00513292 phase3completednot on this map

A Randomized Phase III Trial Comparing a Neoadjuvant Regimen of FEC-75 Followed by Paclitaxel Plus Trastuzumab With a Neoadjuvant Regimen of Paclitaxel Plus Trastuzumab Followed by FEC-75 Plus Trastuzumab in Patients With HER-2 Positive Operable Breast Cancer

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2007 to 2013Enrolled280ConditionsHER2/Neu Positive, Stage IA Breast Cancer, Stage IB Breast Cancer, Stage II Breast CancerArmsCyclophosphamide, Epirubicin Hydrochloride, Laboratory Biomarker Analysis, Paclitaxel, Therapeutic Conventional Surgery
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 2 syntheses or guidelines pooled it, 72 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. NSABP B-41, a Randomized Neoadjuvant Trial: Genes and Signatures Associated with Pathologic Complete Response.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Trial
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  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Oncogenic gene fusions in cancer: from biology to therapy.Signal transduction and targeted therapy · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

17 authors at 9 institutions in 2 countries.

R LesurfMcDonnell Genome Institute at Washington University School of Medicine, St Louis, USA
O L GriffithMcDonnell Genome Institute at Washington University School of Medicine, St Louis, USA
M GriffithMcDonnell Genome Institute at Washington University School of Medicine, St Louis, USA
J HundalMcDonnell Genome Institute at Washington University School of Medicine, St Louis, USA
L TraniMcDonnell Genome Institute at Washington University School of Medicine, St Louis, USA
M A WatsonDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis.
R AftSiteman Cancer Center, Washington University School of Medicine, St Louis, USA
M J EllisMcDonnell Genome Institute at Washington University School of Medicine, St Louis, USA
D OtaDuke University Medical Center, Durham.
V J SumanAlliance Statistics and Data Center, Mayo Clinic, Rochester.
F Meric-BernstamThe University of Texas MD Anderson Cancer Center, Houston.
A M LeitchThe University of Texas Southwestern Medical Center, Dallas.
J C BougheyMayo Clinic, Rochester, USA
G UnzeitigDoctors Hospital of Laredo, Laredo, USA
A U BuzdarThe University of Texas MD Anderson Cancer Center, Houston.
K K HuntThe University of Texas MD Anderson Cancer Center, Houston.
E R MardisInstitute for Genomic Medicine, The Research Institute at Nationwide Children's Hospital, Columbus, USA
James S. McDonnell Foundation · USThe University of Texas MD Anderson Cancer Center · USUniversity Hospitals Seidman Cancer Center · USDoctors Hospital of Laredo · USDuke Medical Center · USMayo Clinic in Florida · USThe Ohio State University · USThe University of Texas Southwestern Medical Center · USWashington University in St. Louis · US

Funding

Large Scale Genome SequencingU54HG003079 · NHGRI · WASHINGTON UNIVERSITY · PI DUTCHER, SUSAN K · 2004 to 2016
$445.7M
Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Statistics CoreU10CA180882 · NCI · MAYO CLINIC ROCHESTER · PI Sumithra Jay Mandrekar · 2014 to 2026
$115.0M
AMERICAN COLLEGE OF SURGEONS ONCOLOGY TRIALS GROUPU10CA076001 · NCI · DUKE UNIVERSITY · PI BERTAGNOLLI, MONICA M · 1998 to 2013
$62.1M
THE ALLIANCE NCTN BIOREPOSITORY AND BIOSPECIMEN RESOURCEU24CA196171 · NCI · WASHINGTON UNIVERSITY · PI Mine Cicek, Wendy Frankel · 2015 to 2026
$35.0M
UT MD Anderson Cancer Center Network Lead Academic Participating Site (LAP) UG1UG1CA233329 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KELLY K HUNT, CHELSEA Camille PINNIX · 2019 to 2026
$11.1M
Washington University/ Siteman Cancer Center Lead Academic SiteU10CA180833 · NCI · WASHINGTON UNIVERSITY · PI BARTLETT, NANCY L, KOZOWER, BENJAMIN D · 2014 to 2018
$7.6M
UT MD Anderson Cancer Center Network Lead Academic Participating Site (LAP)U10CA180858 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HUNT, KELLY K, PINNIX, CHELSEA CAMILLE · 2014 to 2018
$5.6M
Integrated Analysis & Interpretation of Whole Genome Exome & Transcriptome SequenR00HG007940 · NHGRI · WASHINGTON UNIVERSITY · PI GRIFFITH, MALACHI · 2017 to 2019
$724k
DEFINING THE REGULATORY, NON-CODING, MUTATIONAL LANDSCAPE OF BREAST CANCERK22CA188163 · NCI · WASHINGTON UNIVERSITY · PI GRIFFITH, OBI L. · 2014 to 2016
$515k
INTEGRATED ANALYSIS & INTERPRETATION OF WHOLE GENOME, EXOME & TRANSCRIPTOME SEQUENCE DATA IN CANCERK99HG007940 · NHGRI · WASHINGTON UNIVERSITY · PI GRIFFITH, MALACHI · 2015 to 2016
$264k
NCI NIH HHS K22 CA188163NCI NIH HHS P30 CA016058NCI NIH HHS U10 CA076001NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180833NCI NIH HHS U10 CA180858NCI NIH HHS U10 CA180882NCI NIH HHS U24 CA196171NCI NIH HHS UG1 CA233329NHGRI NIH HHS K99 HG007940NHGRI NIH HHS R00 HG007940NHGRI NIH HHS U54 HG003079
6 · The paper itself

Abstract

Background: HER2 (ERBB2) gene amplification and its corresponding overexpression are present in 15-30% of invasive breast cancers. While HER2-targeted agents are effective treatments, resistance remains a major cause of death. The American College of Surgeons Oncology Group Z1041 trial (NCT00513292) was designed to compare the pathologic complete response (pCR) rate of distinct regimens of neoadjuvant chemotherapy and trastuzumab, but ultimately identified no difference. Patients and methods: In supplement to tissues from 37 Z1041 cases, 11 similarly treated cases were obtained from a single institution study (NCT00353483). We have extracted genomic DNA from both pre-treatment tumor biopsies and blood of these 48 cases, and performed whole genome (WGS) and exome sequencing. Coincident with these efforts, we have generated RNA-seq profiles from 42 of the tumor biopsies. Among patients in this cohort, 24 (50%) achieved a pCR. Results: We have characterized the genomic landscape of HER2-positive breast cancer and investigated associations between genomic features and pCR. Cases assigned to the HER2-enriched subtype by RNA-seq analysis were more likely to achieve a pCR compared to the luminal, basal-like, or normal-like subtypes (19/27 versus 3/15; P = 0.0032). Mutational events led to the generation of putatively active neoantigens, but were overall not associated with pCR. ERBB2 and GRB7 were the genes most commonly observed in fusion events, and genomic copy number analysis of the ERBB2 locus indicated that cases with either no observable or low-level ERBB2 amplification were less likely to achieve a pCR (7/8 versus 17/40; P = 0.048). Moreover, among cases that achieved a pCR, tumors consistently expressed immune signatures that may contribute to therapeutic response. Conclusion: The identification of these features suggests that it may be possible to predict, at the time of diagnosis, those HER2-positive breast cancer patients who will not respond to treatment with chemotherapy and trastuzumab. ClinicalTrials.gov identifiers: NCT00513292, NCT00353483.

Indexed as

AgedAntineoplastic Agents, ImmunologicalBreast NeoplasmsChemotherapy, AdjuvantDNA Copy Number VariationsErb-b2 Receptor Tyrosine KinasesFemaleGenetic Association StudiesGenome, HumanGerm-Line MutationHumansINDEL MutationMiddle AgedNeoadjuvant TherapyPolymorphism, Single NucleotideTrastuzumabAntineoplastic Agents, ImmunologicalERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesTrastuzumabbreast cancerERBB2HER2pathologic complete responseresidual diseasetrastuzumab

Identifiers

PMID28453704
PMCPMC5790063
OpenAlexW2589558051

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.