Evidence map›Paper›PMID 37409516›Full record

ArticleCancer medicine2023

Compliance to genomic test recommendations to guide adjuvant chemotherapy decision-making in the case of hormone receptor-positive, human epidermal growth factor receptor 2-negative breast cancer, in real-life settings.

D Hequet, N Hajjaji, E Charafe-Jauffret, A Boucrauta, F Dalenc, V Nicolai, J Lopez, O Tredan, E Deluche, V Fermeaux and 5 more

Abstract read
In one paragraph

Article in Cancer medicine, 2023. 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

15 authors.

D HequetSurgery Department, Institut Curie, St. Cloud, France.ORCID 0000-0001-8926-5651
N HajjajiBreast Cancer Department, Oscar Lambret Cancer Center, Lille, France.
E Charafe-JauffretDepartment of Biopathology, Institut Paoli Calmettes, Marseille, France.
A BoucrautaDepartment of Biopathology, Institut Paoli Calmettes, Marseille, France.
F DalencDepartment of Medical Oncology, Institut universitaire du cancer-oncopole, Institut Claudius-Regaud, Toulouse, France.
V NicolaiDepartment of Medical Oncology, Institut universitaire du cancer-oncopole, Institut Claudius-Regaud, Toulouse, France.
J LopezDepartment of Biopathology, Hospices Civiles de Lyon, Lyon, France.
O TredanDepartment of Medical Oncology, Centre Leon Berard, Lyon, France.
E DelucheDepartment of Medical Oncology, CHU, Limoges, France.ORCID 0000-0001-8474-3116
V FermeauxDepartment of Biopathology, CHU, Limoges, France.
L TixierDepartment of Biopathology, Center Jean Perrin, Clermont Ferrand, France.
A CayreDepartment of Biopathology, Center Jean Perrin, Clermont Ferrand, France.
E MenetPathology Department, Institut Curie, St. Cloud, France.
F LereboursOncology Department, Institut Curie, St. Cloud, France.
R RouzierSurgery Department, Centre François Baclesse, Caen, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenomic tests are a useful tool for adjuvant chemotherapy decision-making in the case of hormone receptor-positive (HR+), and human epidermal growth factor receptor 2-negative (HER2-) breast cancer with intermediate prognostic factors. Real-life data on the use of tests can help identify the target population for testing.

methodsFrench multicentric study (8 centers) including patients, all candidates for adjuvant chemotherapy for HR-positive, HER2-negative early breast cancer. We describe the percentage of tests performed outside recommendations, according to the year of testing. We calculated a ratio defined as the number of tests required to avoid chemotherapy for one patient, and according to patient and cancer characteristics. We then performed a cost-saving analysis using medical cost data over a period of 1 year from diagnosis, calculated from a previous study. Finally, we calculated the threshold of the ratio (number of tests required to avoid chemotherapy for one patient) below which the use of genomic tests was cost-saving.

resultsA total of 2331 patients underwent a Prosigna test. The ratio (performed test/avoided chemotherapy) was 2.8 [95% CI: 2.7-2.9] in the whole population. In the group following recommendations for test indication, the ratio was 2.3 [95% CI: 2.2-2.4]. In the case of non-abidance by recommendations, the ratio was 3 [95% CI: 2.8-3.2]. Chemotherapy was avoided in 841 patients (36%) following the results of the Prosigna test. The direct medical costs saved over 1 year of care were 3,878,798€ and 1,718,472€ in the group of patients following test recommendations. We calculated that the ratio (performed test/avoided chemotherapy) needed to be under 6.9 for testing to prove cost-saving.

conclusionThe use of genomic testing proved cost-saving in this large multicentric real-life analysis, even in certain cases when the test was performed outside recommendations.

Indexed as

Triple Negative Breast NeoplasmsChemotherapy, AdjuvantErb-b2 Receptor Tyrosine KinasesFemaleGenomicsHumansERBB2 protein, humanErb-b2 Receptor Tyrosine Kinasesbreast cancerdeescalationgenomic testsguidelines

Identifiers

PMID37409516
PMCPMC10501273

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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.