Evidence map›Paper›PMID 42461910›Full record

ArticlePloS one2026

Real-world implementation and cost impact analysis of Oncotype DX testing in early-stage breast cancer.

Niina Mäenpää, Leena Tiainen, Janne Martikainen, Minna Tanner, Arja Jukkola, Maarit Bärlund

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Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Niina MäenpääFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID https://orcid.org/0009-0002-4983-1879
Leena TiainenFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID https://orcid.org/0000-0003-4247-8523
Janne MartikainenSchool of Pharmacy, University of Eastern Finland, Kuopio, Finland.
Minna TannerDepartment of Oncology, Tays Cancer Centre, Tampere University Hospital, The Wellbeing Services County of Pirkanmaa, Tampere, Finland.
Arja JukkolaFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Maarit BärlundFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe decision on appropriate adjuvant treatment for patients with hormone receptor-positive (HR+) and human epidermal growth factor receptor 2 -negative (HER2-) early breast cancer (eBC) is sometimes challenging. Genomic assays have improved individualized treatment decisions by providing information on the genomic risk of tumors. The Oncotype DX assay (ODX) is both prognostic and predictive of chemotherapy benefit. This study aimed to evaluate the implementation process of the ODX into clinical practice, the impact of ODX on adjuvant chemotherapy treatment decisions and conduct a cost impact analysis. PATIENTS AND

methodsA retrospective study at Tampere University Hospital included 129 patients with HR + , HER2- eBC tested with ODX between September 2021 and September 2023. Treatment decisions as well as adjuvant chemotherapy (CT) costs, associated health provider costs, and societal costs were projected.

resultsODX testing significantly altered CT recommendations by reducing unnecessary CT for 73% of the study patients. With ODX testing, the cost impact analysis revealed partial cost savings for the health care provider due to reduced CT administration. From a societal perspective, the use of ODX resulted in substantial savings largely attributed to the maintenance of work productivity among working-aged and employed patients.

conclusionThis study highlights the importance of streamlined testing processes and the need for clinician training in interpreting test results in a real-world setting. In addition, the findings underscore the role of ODX in enhancing personalized treatment in HR + , HER2- eBC while reducing overtreatment. The cost analysis indicates substantial cost savings with ODX testing.

Indexed as

Breast NeoplasmsAdultAgedChemotherapy, AdjuvantCost-Benefit AnalysisErb-b2 Receptor Tyrosine KinasesFemaleGene Expression ProfilingHumansMiddle AgedNeoplasm StagingRetrospective StudiesErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID42461910
PMCPMC13374984

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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.