Evidence map›Paper›PMID 32140564›Full record

ArticleNPJ breast cancer2020

The Prosigna 50-gene profile and responsiveness to adjuvant anthracycline-based chemotherapy in high-risk breast cancer patients.

Maj-Britt Jensen, Anne-Vibeke Lænkholm, Eva Balslev, Wesley Buckingham, Sean Ferree, Vesna Glavicic, Jeanette Dupont Jensen, Ann Søegaard Knoop, Henning T Mouridsen, Dorte Nielsen and 2 more

Open access · goldAbstract read
In one paragraph

Article in NPJ breast cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

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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

12 authors at 6 institutions in 3 countries.

Maj-Britt JensenDanish Breast Cancer Cooperative Group, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.ORCID 0000-0001-5348-3040
Anne-Vibeke Lænkholm2Department of Surgical Pathology, Zealand University Hospital, Slagelse, Denmark.
Eva BalslevDepartment of Pathology, Herlev and Gentofte Hospital, University of Copenhagen, Herlev, Denmark.
Wesley BuckinghamNanoString Technologies Inc, Seattle, WA USA.
Sean FerreeNanoString Technologies Inc, Seattle, WA USA.
Vesna Glavicic5Department of Oncology, Zealand University Hospital, Naestved, Denmark.
Jeanette Dupont Jensen6Department of Oncology, Odense University Hospital, Odense, Denmark.
Ann Søegaard KnoopDepartment of Oncology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Henning T Mouridsen *Danish Breast Cancer Cooperative Group, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Dorte NielsenDepartment of Oncology, Herlev and Gentofte Hospital, University of Copenhagen, Herlev, Denmark.
Torsten O Nielsen9Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC Canada.
Bent EjlertsenDanish Breast Cancer Cooperative Group, Department of Oncology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Copenhagen University Hospital · DKNanostring Technologies (United States) · USUniversity of Copenhagen · DKZealand University Hospital · DKOdense University Hospital · DKUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The DBCG89D trial randomized high-risk early breast cancer patients to adjuvant CMF (cyclophosphamide, methotrexate and fluorouracil) or CEF (cyclophosphamide, epirubicin and fluorouracil). Prosigna assays were performed by researchers with no access to clinical data. Time to distant recurrence (DR) was the primary endpoint, time to recurrence (TR) and overall survival (OS) secondary. Among the 980 Danish patients enrolled, Prosigna results were obtained in 686. Continuous ROR score was associated with DR for CMF (adjusted hazard ratio (HR) 1.20, 95% CI 1.09-1.33), and for CEF (HR 1.04, 95% CI 0.92-1.18),

Indexed as

Predictive markersRandomized controlled trials

Identifiers

PMID32140564
PMCPMC7044229
OpenAlexW3008259997

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.