Evidence map›Paper›PMID 28407247›Full record

Trial reportJournal of surgical oncology2017

Using the 21-gene assay from core needle biopsies to choose neoadjuvant therapy for breast cancer: A multicenter trial.

Harry D Bear, Wen Wan, André Robidoux, Peter Rubin, Steven Limentani, Richard L White, James Granfortuna, Judith O Hopkins, Dwight Oldham, Angel Rodriguez and 1 more

Erratum issuedAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of surgical oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
–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

49 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
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  12. Hormone Receptor-Positive HER2-Negative/MammaPrint High-2 Breast Cancers Closely Resemble Triple-Negative Breast Cancers.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Standardized Definitions for Efficacy End Points in Neoadjuvant Breast Cancer Clinical Trials: NeoSTEEP.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Article
  18. Article
  19. Article
  20. Frontiers in oncology · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Harry D BearVirginia Commonwealth University and Massey Cancer Center, Richmond, Virginia.ORCID http://orcid.org/0000-0002-7632-9019
Wen WanVirginia Commonwealth University and Massey Cancer Center, Richmond, Virginia.
André RobidouxCentre Hospitalier de l'Universite de Montreal, Montreal, Quebec, Canada.
Peter RubinCone Health Cancer Center, Greensboro, North Carolina.
Steven LimentaniCarolinas Medical Center, Charlotte, North Carolina.
Richard L WhiteCarolinas Medical Center, Charlotte, North Carolina.ORCID http://orcid.org/0000-0001-6559-8312
James GranfortunaCone Health Cancer Center, Greensboro, North Carolina.
Judith O HopkinsForsyth Regional Cancer Center, Winston Salem, North Carolina.
Dwight OldhamLynchburg Hematology Oncology Clinic, Lynchburg, Virginia.
Angel RodriguezMethodist Hospital, Houston, Texas.
Amy P SingGenomic Health, Inc., Redwood City, California.

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Keri R Maher · 1985 to 2026
$51.0M
NCI NIH HHS P30 CA016059
6 · The paper itself

Abstract

objectiveWe hypothesized that the Oncotype Dx

methodsThis study enrolled patients with HR+, HER2-negative, invasive breast cancers not suitable for BCS (size ≥ 2 cm). Core needle biopsy blocks were tested. For tumors with RS < 11, patients received hormonal therapy (NHT); patients with RS > 25 tumors received chemotherapy (NCT); patients with RS 11-25 were randomized to NHT or NCT. Primary endpoint was whether 1/3 or more of randomized patients refused assigned treatment.

resultsSixty-four patients were enrolled. Of 33 patients with RS 11-25, 5 (15%) refused assignment to NCT. This was significantly lower than the 33% target (binomial test, P = 0.0292). Results for clinical outcomes (according to treatment received for 55 subjects) included successful BCS for 75% of tumors with RS < 11 receiving NHT, 72% for RS 11-25 receiving NHT, 64% for RS 11-25 receiving NCT, and 57% for RS > 25 receiving NCT.

conclusionsUsing the RS to guide NST is feasible. These results suggest that for patients with RS < 25 NHT is a potentially effective strategy.

Indexed as

Mastectomy, SegmentalAdultAgedAged, 80 and overAntineoplastic AgentsAromatase InhibitorsBiopsy, Large-Core NeedleBreast NeoplasmsChemotherapy, AdjuvantClinical Decision-MakingFemaleGene Expression ProfilingHumansMiddle AgedNeoadjuvant TherapyPilot ProjectsAntineoplastic AgentsAromatase InhibitorsReceptors, EstrogenReceptors, Progesteronebreast cancerchemotherapygene expressionhormonal therapyneoadjuvant

Identifiers

PMID28407247
PMCPMC5481477

What OpenQuestion holds

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Registered trials

None linked

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.