Evidence map›Paper›PMID 38308000›Full record

ArticleBritish journal of cancer2024

A UK prospective multicentre decision impact, decision conflict and economic evaluation of the 21-gene assay in women with node+ve, hormone receptor+ve, HER2-ve breast cancer.

Simon Holt, Mark Verrill, Laura Pettit, Anna Rigg, Tamas Hickish, Caroline Archer, Jo Dent, Marianne Dillon, Mark Nathan, Ludger Barthelmes and 5 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in British journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 2 syntheses or guidelines pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Observational
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

15 authors at 12 institutions in 2 countries.

Simon HoltSwansea University, Swansea, UK. simon_holt@mac.com.ORCID 0000-0003-1118-0150
Mark VerrillNorthern Centre for Cancer Care, Newcastle, UK.ORCID 0000-0002-8676-1120
Laura PettitRoyal Shrewsbury Hospital, Shrewsbury, UK.
Anna RiggGuy's and St Thomas' Hospitals, London, UK.
Tamas HickishUniversity Hospitals Dorset, Bournemouth, UK.
Caroline ArcherPortsmouth Hospitals University NHS Trust, Portsmouth, UK.
Jo DentHuddersfield NHS Trust, Huddersfield, UK.
Marianne DillonYork Hospital, York, UK.
Mark NathanGuy's and St Thomas' Hospitals, London, UK.
Ludger BarthelmesCumberland Infirmary, Carlisle, UK.
Shazza RehmanAiredale NHS Foundation Trust, Keighley, UK.
Yousef SharaihaPrince Philip Hospital, Llanelli, UK.
Paige InnisExact Sciences Corporation, Redwood City, CA, USA.
Priya Sai-GiridharPrince Philip Hospital, Llanelli, UK.
Saira KhawajaPrince Philip Hospital, Llanelli, UK.
Prince Philip Hospital · GBSt Thomas' Hospital · GBAiredale NHS Foundation Trust · GBBournemouth University · GBCalderdale and Huddersfield NHS Foundation Trust · GBCumberland Infirmary · GBExact Sciences (United States) · USNorthern Health and Social Care Trust · GBPortsmouth Hospitals NHS Trust · GBRoyal Shrewsbury Hospital · GBSwansea University · GBYork Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFor a tumour profiling test to be of value, it needs to demonstrate that it is changing clinical decisions, improving clinical confidence, and of economic benefit. This trial evaluated the use of the Oncotype DX Breast Recurrence Score® assay against these criteria in 680 women with hormone receptor-positive (HR+), HER2-negative early breast cancer with 1-3 lymph nodes positive (LN+) in the UK National Health Service (NHS).

methodsPrior to receipt of the Recurrence Score (RS) result, both the physician and the patient were asked to state their preference for or against chemotherapy and their level of confidence on a scale of 1-5. Following receipt of the RS result, the physician and patient were asked to make a final decision regarding chemotherapy and record their post-test level of confidence.

resultsReceipt of the RS result led to a 51.5% (95% CI, 47.2-55.8%) reduction in chemotherapy, significantly increased the relative and absolute confidence for both physicians and patients and led to an estimated saving to the NHS of £787 per patient.

conclusionThe use of the Oncotype DX assay fulfils the criteria of changing clinical decisions, improving confidence and saving money.

Indexed as

Breast NeoplasmsChemotherapy, AdjuvantCost-Benefit AnalysisFemaleGene Expression ProfilingHormonesHumansNeoplasm Recurrence, LocalProspective StudiesState MedicineUnited KingdomHormones

Identifiers

PMID38308000
PMCPMC10991515
OpenAlexW4391474741

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.