Evidence map›Paper›PMID 39349887›Full record

ArticleBreast cancer research and treatment2025

70-Gene signature-guided adjuvant systemic treatment adjustments in early-stage ER+ breast cancer patients: 7-year follow-up of a prospective multicenter cohort study.

Eline E F Verreck, Anne Kuijer, Julia E C van Steenhoven, José H Volders, Annette W G van der Velden, Sabine Siesling, Anja N H Timmer-Bonte, Tineke J Smilde, Alex L T Imholz, Charlotte F J M Blanken-Peeters and 12 more

Abstract readMulticenter Study
In one paragraph

Article in Breast cancer research and treatment, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

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

2 citing papers in PubMed.

  1. Article
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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

22 authors.

Eline E F VerreckUniversity Utrecht, Utrecht, the Netherlands. e.verreck@erasmusmc.nl.
Anne KuijerDepartment of Surgery, St. Antonius Hospital, Nieuwegein, the Netherlands.
Julia E C van SteenhovenDepartment of Surgery, Diakonessenhuis, Bosboomstraat 1, 3582 KE, Utrecht, the Netherlands.
José H VoldersDepartment of Surgery, Diakonessenhuis, Bosboomstraat 1, 3582 KE, Utrecht, the Netherlands.
Annette W G van der VeldenDepartment Internal Medicine, Martini Hospital, Groningen, the Netherlands.
Sabine SieslingDepartment of Health Technology and Services Research, Technical Medical Centre, University of Twente, Enschede, the Netherlands.
Anja N H Timmer-BonteDepartment Internal Medicine, Alexander Monro Hospital, Bilthoven, the Netherlands.
Tineke J SmildeDepartment Internal Medicine, Jeroen Bosch Hospital, Den Bosch, the Netherlands.
Alex L T ImholzDepartment Internal Medicine, Deventer Hospital, Deventer, the Netherlands.
Charlotte F J M Blanken-PeetersDepartment of Surgery, Rijnstate Hospital Arnhem, Arnhem, the Netherlands.
Bart de ValkDeparment Internal Medicine, Spaarne Gasthuis, Hoofddorp, the Netherlands.
Suzan VrijaldenhovenDepartment Internal Medicine, Noordwest Ziekenhuisgroep, Alkmaar, the Netherlands.
Willem B LastdragerDepartment of Surgery, Gelre Hospital, Apeldoorn, the Netherlands.
Annebeth W HaringhuizenDeparmtent Internal Medicine, Gelderse Vallei Hospital, Ede, the Netherlands.
Jarmo C B HuntingDepartment Internal Medicine, St. Antonius Hospital, Nieuwegein, the Netherlands.
Sjoerd HovengaDepartment Internal Medicine, Nij Smellinghe Hospital, Drachten, the Netherlands.
Peter NieboerDeparment Internal Medicine, Wilhemina Hospital, Assen, the Netherlands.
Hanneke M ZuetenhorstDeparment Internal Medicine, Franciscus Gasthuis, Rotterdam, the Netherlands.
Geert W M TetterooDepartment of Surgery, Ijsselland Hospital, Cappele Aan de Ijssel, the Netherlands.
Carolien H SmorenburgDepartment Internal Medicine, Antoni Van Leeuwenhoek Hospital, Amsterdam, the Netherlands.
Marissa C van MaarenDepartment of Health Technology and Services Research, Technical Medical Centre, University of Twente, Enschede, the Netherlands.
Thijs van DalenDepartment of Surgery, Erasmus Medical Centre, Dr. Molewaterplein 40, 3015 GD, Rotterdam, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA previous prospective multicenter study revealed the change of the oncologists' chemotherapy advice due to the 70-Gene signature (GS) test result in half of the estrogen receptor-positive (ER+) invasive early-stage breast cancer patients with disputable chemotherapy indication. This resulted in less patients receiving chemotherapy. This study aims to complement these results by the 7-year oncological outcomes according to the 70-GS test result and the oncologists' pre-test advice.

methodsPatients operated for early-stage ER+ breast cancer with disputable chemotherapy indication, had been prospectively included between 2013 and 2015. Oncologists were asked whether they intended to administer adjuvant chemotherapy before deployment of the 70-GS test. Information on adjuvant systemic treatment and oncological outcome was obtained through active follow-up by data managers of the Netherlands Cancer Registry. The primary endpoint of this study was distant metastasis-free survival (DMFS) according to the genomic risk. Exploratory analyses were done to evaluate DMFS in relation to the oncologists' pre-test advice.

resultsAfter a median follow-up of 7 years, distant metastases were diagnosed in 23 of the 606 patients (3.8%) and 36 (5.9%) patients had died. The DMFS rate for the 357 70-GS genomic low-risk patients was 94.2% (95% CI 91.2-96.2) and 89.1% for the 249 genomic high-risk patients (95% CI 84.3-92.4). Of the low-risk patients 3% had received chemotherapy compared to 80% of the high-risk patients. For the subgroups based on the pre-test oncologists' advice (no chemotherapy/chemotherapy/unsure) there were no clinically relevant differences in DMFS (89.8, 93.2 and 92.0%, respectively), while comparable proportions of patients had received chemotherapy.

conclusionsIn patients with early-stage ER+ breast cancer with a disputable chemotherapy indication it is sensible to deploy the 70-GS to better select patients for adjuvant chemotherapy.

Indexed as

Biomarkers, TumorBreast NeoplasmsReceptors, EstrogenTranscriptomeAdultAgedAntineoplastic Combined Chemotherapy ProtocolsChemotherapy, AdjuvantFemaleFollow-Up StudiesGene Expression ProfilingHumansMiddle AgedNeoplasm StagingProspective StudiesTreatment OutcomeBiomarkers, TumorReceptors, Estrogen70-Gene SignatureChemotherapy decisionLuminal breast cancer

Identifiers

PMID39349887
PMCPMC11785635

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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.