Evidence map›Paper›PMID 26429296›Full record

ArticleBreast cancer research : BCR2015

The relationship between quantitative human epidermal growth factor receptor 2 gene expression by the 21-gene reverse transcriptase polymerase chain reaction assay and adjuvant trastuzumab benefit in Alliance N9831.

Edith A Perez, Frederick L Baehner, Steven M Butler, E Aubrey Thompson, Amylou C Dueck, Farid Jamshidian, Diana Cherbavaz, Carl Yoshizawa, Steven Shak, Peter A Kaufman and 4 more

Registry-linked trialAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00005970 (Phase III Trial of Doxorubicin and Cyclophosphamide), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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.

NCT00005970 phase3completednot on this map

Phase III Trial of Doxorubicin and Cyclophosphamide (AC) Followed by Weekly Paclitaxel With or Without Trastuzumab as Adjuvant Treatment for Women With HER-2 Over-Expressing or Amplified Node Positive or High-Risk Node Negative Breast Cancer

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2000 to 2010Enrolled3,436ConditionsBreast Adenocarcinoma, HER2 Positive Breast Carcinoma, Stage IA Breast Cancer AJCC v7, Stage IB Breast Cancer AJCC v7ArmsAromatase Inhibition Therapy, Cyclophosphamide, Doxorubicin Hydrochloride, Laboratory Biomarker Analysis, Paclitaxel
3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. A predictor of response in HER2+ breast cancer-at last!Journal of the National Cancer Institute · 2023
    Article
  5. Article
  6. Review
  7. Observational
  8. Article
  9. Article
  10. Article
  11. Relationship betweenOncoTargets and therapy · 2018
    Article
  12. Article
  13. Article
  14. Review
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

14 authors.

Edith A PerezMayo Clinic, 4500 San Pablo Rd, Jacksonville, FL, 32224, USA. perez.edith@mayo.edu.
Frederick L BaehnerGenomic Health, Inc, 301 Penobscot Drive, Redwood City, CA, 94063, USA. RBaehner@genomichealth.com.
Steven M ButlerGenomic Health, Inc, 301 Penobscot Drive, Redwood City, CA, 94063, USA. smbutler@genomichealth.com.
E Aubrey ThompsonMayo Clinic, 4500 San Pablo Rd, Jacksonville, FL, 32224, USA. thompson.aubrey@mayo.edu.
Amylou C DueckAlliance Statistics and Data Center, Mayo Clinic, 13400 E. Shea Boulevard, Scottsdale, AZ, USA. Dueck.Amylou@mayo.edu.
Farid JamshidianGenomic Health, Inc, 301 Penobscot Drive, Redwood City, CA, 94063, USA. FJamshidian@genomichealth.com.
Diana CherbavazGenomic Health, Inc, 301 Penobscot Drive, Redwood City, CA, 94063, USA. DCherbavaz@genomichealth.com.
Carl YoshizawaGenomic Health, Inc, 301 Penobscot Drive, Redwood City, CA, 94063, USA. CYoshizawa@genomichealth.com.
Steven ShakGenomic Health, Inc, 301 Penobscot Drive, Redwood City, CA, 94063, USA. sshak@genomichealth.com.
Peter A KaufmanNorris Cotton Cancer Center, Dartmouth-Hitchcock Medical Center, 1 Medical Center Drive, Lebanon, NH, 03766, USA. Peter.A.Kaufman@hitchcock.org.
Nancy E DavidsonUniversity of Pittsburgh Cancer Institute, 5150 Centre Avenue, Pittsburgh, PA, 15232, USA. davidsonne@upmc.edu.
Julie GralowSeattle Cancer Care Alliance, 825 Eastlake Avenue East, Seattle, WA, 98109, USA. pink@u.washington.edu.
Yan W AsmannMayo Clinic, 4500 San Pablo Rd, Jacksonville, FL, 32224, USA. Asmann.Yan@mayo.edu.
Karla V BallmanAlliance Statistics and Data Center, 200 1st Street SW, Mayo Clinic, Rochester, MN, 55905, USA. Ballman.Karla@mayo.edu.

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
Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
TRANSLATIONAL RESEARCHU10CA025224 · NCI · MAYO CLINIC ROCHESTER · PI BUCKNER, JAN C · 1985 to 2013
$85.0M
THE ALLIANCE NCTN BIOREPOSITORY AND BIOSPECIMEN RESOURCEU24CA196171 · NCI · WASHINGTON UNIVERSITY · PI Mine Cicek, Wendy Frankel · 2015 to 2026
$35.0M
Therapuetic Immune Targeting of EphA2 Expressed by Melanoma & Its Tumor-AssociateP50CA121973 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KIRKWOOD, JOHN MUNN · 2008 to 2018
$22.9M
NCI NCTN-Network Lead Academic Participating Site at UPMC Hillman Cancer CenterUG1CA233184 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ADAM M BRUFSKY, John Munn Kirkwood · 2019 to 2026
$7.7M
NCI NCTN-Network Lead Academic Site at UPCIU10CA180844 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BRUFSKY, ADAM M, EDWARDS, ROBERT PAGE · 2014 to 2018
$4.5M
Predictive Biomarkers of Adjuvant Trastuzumab in the HER2+N9831 Intergroup TrialR01CA129949 · NCI · MAYO CLINIC JACKSONVILLE · PI PEREZ, EDITH A. · 2008 to 2011
$1.3M
NCI NIH HHS P30 CA023108NCI NIH HHS P50 CA121973NCI NIH HHS R01 CA129949NCI NIH HHS U10 CA025224NCI NIH HHS U10-CA025224NCI NIH HHS U10 CA180821NCI NIH HHS U10-CA180821NCI NIH HHS U10 CA180844NCI NIH HHS U10 CA180882NCI NIH HHS U10-CA180882NCI NIH HHS U24 CA196171NCI NIH HHS UG1 CA233184
6 · The paper itself

Abstract

introductionThe N9831 trial demonstrated the efficacy of adjuvant trastuzumab for patients with human epidermal growth factor receptor 2 (HER2) locally positive tumors by protein or gene analysis. We used the 21-gene assay to examine the association of quantitative HER2 messenger RNA (mRNA) gene expression and benefit from trastuzumab.

methodsN9831 tested the addition of trastuzumab to chemotherapy in stage I-III HER2-positive breast cancer. For two of the arms of the trial, doxorubicin and cyclophosphamide followed by paclitaxel (AC-T) and doxorubicin and cyclophosphamide followed by paclitaxel and trastuzumab concurrent chemotherapy-trastuzumab (AC-TH), recurrence score (RS) and HER2 mRNA expression were determined by the 21-gene assay (Oncotype DX®) (negative <10.7, equivocal 10.7 to <11.5, and positive ≥11.5 log2 expression units). Cox regression was used to assess the association of HER2 expression with trastuzumab benefit in preventing distant recurrence.

resultsMedian follow-up was 7.4 years. Of 1,940 total patients, 901 had consent and sufficient tissue. HER2 by reverse transcriptase polymerase chain reaction (RT-PCR) was negative in 130 (14 %), equivocal in 85 (9 %), and positive in 686 (76 %) patients. Concordance between HER2 assessments was 95 % for RT-PCR versus central immunohistochemistry (IHC) (>10 % positive cells = positive), 91 % for RT-PCR versus central fluorescence in situ hybridization (FISH) (≥2.0 = positive) and 94 % for central IHC versus central FISH. In the primary analysis, the association of HER2 expression by 21-gene assay with trastuzumab benefit was marginally nonsignificant (nonlinear p = 0.057). In hormone receptor-positive patients (local IHC) the association was significant (p = 0.002). The association was nonlinear with the greatest estimated benefit at lower and higher HER2 expression levels.

conclusionsConcordance among HER2 assessments by central IHC, FISH, and RT-PCR were similar and high. Association of HER2 mRNA expression with trastuzumab benefit as measured by time to distant recurrence was nonsignificant. A consistent benefit of trastuzumab irrespective of mHER2 levels was observed in patients with either IHC-positive or FISH-positive tumors. Trend for benefit was observed also for the small groups of patients with negative results by any or all of the central assays.

trial registrationClinicaltrials.gov NCT00005970 . Registered 5 July 2000.

Indexed as

AdolescentAdultAntineoplastic AgentsBreast NeoplasmsDisease-Free SurvivalDrug Resistance, NeoplasmErb-b2 Receptor Tyrosine KinasesFemaleGene ExpressionHumansMiddle AgedNeoplasm Recurrence, LocalProportional Hazards ModelsRandomized Controlled Trials as TopicReverse Transcriptase Polymerase Chain ReactionTrastuzumabAntineoplastic AgentsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesTrastuzumab

Identifiers

PMID26429296
PMCPMC4589954

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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.