Evidence map›Paper›PMID 19620488›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2009

Outcome of patients with early-stage breast cancer treated with doxorubicin-based adjuvant chemotherapy as a function of HER2 and TOP2A status.

Raymond Tubbs, William E Barlow, G Thomas Budd, Eric Swain, Peggy Porter, Allen Gown, I-Ten Yeh, George Sledge, Charles Shapiro, James Ingle and 4 more

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

26 citing papers in PubMed, 65 citations in OpenAlex.

  1. Trial
  2. Alteration of topoisomerase II-alpha gene in human breast cancer: association with responsiveness to anthracycline-based chemotherapy.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2011
    Trial
  3. Trial
  4. Article
  5. Article
  6. Review
  7. Article
  8. Validation of the DNA Damage Immune Response Signature in Patients With Triple-Negative Breast Cancer From the SWOG 9313c Trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2019
    Article
  9. Article
  10. Chemical Composition and Antiproliferative Effects of a Methanol Extract ofEvidence-based complementary and alternative medicine : eCAM · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Novel points of attack for targeted cancer therapy.Basic & clinical pharmacology & toxicology · 2015
    Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 1 institution in 1 country.

Raymond TubbsDepartment of Molecular Pathology, Cleveland Clinic, Cleveland, OH 44195, USA. TubbsR@ccf.org
William E Barlow
G Thomas Budd
Eric Swain
Peggy Porter
Allen Gown
I-Ten Yeh
George Sledge
Charles Shapiro
James Ingle
Charles Haskell
Kathy S Albain
Robert Livingston
Daniel F Hayes
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · US

Funding

CANCER AND LEUKEMIA GROUP B MINORITY SATELLITE SUPPLEMENU10CA031946 · NCI · UNIVERSITY OF CHICAGO · PI BERTAGNOLLI, MONICA M · 1985 to 2013
$158.4M
SWOG - Foreign Accrual under UMiU10CA032102 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BLANKE, CHARLES D. · 1985 to 2013
$141.3M
TRANSLATIONAL RESEARCHU10CA025224 · NCI · MAYO CLINIC ROCHESTER · PI BUCKNER, JAN C · 1985 to 2013
$85.0M
SOUTHWEST ONCOLOGY GROUP--STATISTICAL CENTERU10CA038926 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEBLANC, MICHAEL L. · 1985 to 2013
$69.8M
COMMUNITY CLINICAL ONCOLOGY PROGRAMU10CA035431 · NCI · VIA CHRISTI REGIONAL MEDICAL CENTER · PI DAKHIL, SHAKER R · 1985 to 2014
$24.0M
UPSTATE CAROLINA COMMUNITY CLINICAL ONCOLOGY PROGRAMU10CA035119 · NCI · SPARTANBURG REGIONAL MEDICAL CENTER · PI BEARDEN, JAMES D · 1985 to 2013
$21.5M
DAYTON CLINICAL ONCOLOGY PROGRAMU10CA035090 · NCI · KETTERING MEDICAL CENTER · PI GROSS, HOWARD M · 1985 to 2014
$12.0M
COMMUNITY CLINICAL ONCOLOGY PROGRAMU10CA035261 · NCI · GRANT/RIVERSIDE METHODIST HOSPITALS · PI KUEBLER, PHILIP J. · 1985 to 2014
$10.6M
WESTERN ONCOLOGY RESEARCH CONSORTIUMU10CA045377 · NCI · PROVIDENCE PORTLAND MEDICAL CENTER · PI CONLIN, ALISON K · 1987 to 2013
$9.9M
Hawaii Minority-Based Clinical Community Oncology ProgramU10CA063844 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI BERENBERG, JEFFREY LEE · 1994 to 2014
$9.0M
OZARKS REGIONAL COMMUNITY CLINICAL ONCOLOGY PROGRAMU10CA045560 · NCI · ST. JOHN'S REGIONAL HEALTH CENTER · PI CARLSON, JAY W · 1987 to 2014
$8.2M
COMMUNITY CLINICAL ONCOLOGY PROGRAMU10CA045450 · NCI · ST. JOSEPH'S HOSPITAL (ATLANTA) · PI SEAY, THOMAS E · 1987 to 2012
$7.6M
NCI NIH HHS CA04920NCI NIH HHS CA12644NCI NIH HHS CA14028NCI NIH HHS CA16385NCI NIH HHS CA20319NCI NIH HHS CA21155NCI NIH HHS CA22433NCI NIH HHS CA25224NCI NIH HHS CA31946NCI NIH HHS CA32291NCI NIH HHS CA35090NCI NIH HHS CA35117NCI NIH HHS CA35192NCI NIH HHS CA35261NCI NIH HHS CA37891NCI NIH HHS CA42777NCI NIH HHS CA45377NCI NIH HHS CA45450NCI NIH HHS CA46113NCI NIH HHS CA46282NCI NIH HHS CA46368NCI NIH HHS CA49883NCI NIH HHS CA52654NCI NIH HHS CA58415NCI NIH HHS CA58416NCI NIH HHS CA58658NCI NIH HHS CA58686NCI NIH HHS CA58861NCI NIH HHS CA63845NCI NIH HHS CA68183NCI NIH HHS CA74647NCI NIH HHS CA76132NCI NIH HHS CA76429NCI NIH HHS CA76447NCI NIH HHS CA76462NCI NIH HHS CA77658NCI NIH HHS N01 CA004919NCI NIH HHS N01 CA013612NCI NIH HHS N01 CA027057NCI NIH HHS N01 CA032102NCI NIH HHS N01 CA035119NCI NIH HHS N01 CA035431NCI NIH HHS N01 CA038926NCI NIH HHS N01 CA045560NCI NIH HHS N01 CA046441NCI NIH HHS N01 CA063844NCI NIH HHS N01 CA067575NCI NIH HHS U10 CA004919NCI NIH HHS U10 CA013612NCI NIH HHS U10 CA014028NCI NIH HHS U10 CA020319NCI NIH HHS U10 CA025224NCI NIH HHS U10 CA027057NCI NIH HHS U10 CA031946NCI NIH HHS U10 CA032102NCI NIH HHS U10 CA032291NCI NIH HHS U10 CA035090NCI NIH HHS U10 CA035119NCI NIH HHS U10 CA035192NCI NIH HHS U10 CA035261NCI NIH HHS U10 CA035431NCI NIH HHS U10 CA038926NCI NIH HHS U10 CA042777NCI NIH HHS U10 CA045377NCI NIH HHS U10 CA045450NCI NIH HHS U10 CA045560NCI NIH HHS U10 CA046282NCI NIH HHS U10 CA046368NCI NIH HHS U10 CA046441NCI NIH HHS U10 CA049883NCI NIH HHS U10 CA052654NCI NIH HHS U10 CA058861NCI NIH HHS U10 CA063844NCI NIH HHS U10 CA063845NCI NIH HHS U10 CA067575NCI NIH HHS U10 CA074647NCI NIH HHS U10 CA077658
6 · The paper itself

Abstract

purposeAmplification and deletion of the TOP2A gene have been reported as positive predictive markers of response to anthracycline-based therapy. We determined the status of the HER2 and TOP2A genes in a large cohort of breast cancer patients treated with adjuvant doxorubicin (A) and cyclophosphamide (C). PATIENTS AND

methodsTOP2A/CEP17 and HER2/CEP17 fluorescent in situ hybridization (FISH) were performed on tissue microarrays (TMAs) constructed from 2,123 of the 3,125 women with moderate-risk primary breast cancer who received equivalent doses of either concurrent adjuvant chemotherapy with A plus C (n = 1,592) or sequential A followed by C (n = 1,533).

resultsAn abnormal TOP2A genotype was identified for 153 (9.4%) of 1,626 patients (4.0% amplified; 5.4% deleted). An abnormal HER2 genotype was identified for 303 (20.4%) of 1,483 patients (18.8% amplified; 1.6% deleted). No significant differences in either overall survival (OS) or disease-free survival (DFS) were identified for TOP2A. In univariate analysis, OS and DFS rates were strongly and adversely associated only with higher levels of HER2 amplification (ratio > or = 4.0). Survival was not associated with low-level HER2 amplification (ratio > or = 2; OS hazard ratio [HR], 1.14; P = .39; DFS HR, 1.07; P = .62), but it was associated for a ratio > or = 4 (OS HR, 1.45; P = .03; DFS HR, 1.38; P = .033), in which analysis was adjusted for menopausal status, hormone receptor status, treatment, number of positive nodes, and tumor size.

conclusionIn this population of patients with early-stage breast cancer who were treated with adjuvant AC chemotherapy, TOP2A abnormalities were not associated with outcome. HER2 high-level amplification was a prognostic marker in anthracycline-treated patients.

Indexed as

Antigens, NeoplasmBreast NeoplasmsChemotherapy, AdjuvantChromosomes, Human, Pair 17DNA-Binding ProteinsDNA Topoisomerases, Type IIDoxorubicinErb-b2 Receptor Tyrosine KinasesFemaleGene AmplificationGene DosageHumansImmunohistochemistryIn Situ Hybridization, FluorescenceNeoplasm StagingPoly-ADP-Ribose Binding ProteinsAntigens, NeoplasmDNA-Binding ProteinsDNA Topoisomerases, Type IIDoxorubicinERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesPoly-ADP-Ribose Binding ProteinsTOP2A protein, human

Identifiers

PMID19620488
PMCPMC2734394
OpenAlexW2162355648

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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.