Evidence map›Paper›PMID 37589218›Full record

ArticleThe oncologist2023

Real-World Impact of Adjuvant Anti-HER2 Treatment on Characteristics and Outcomes of Women With HER2-Positive Metastatic Breast Cancer in the ESME Program.

Fanny Le Du, Matthieu Carton, Thomas Bachelot, Mahasti Saghatchian, Barbara Pistilli, Etienne Brain, Delphine Loirat, Laurence Vanlemmens, Thomas Vermeulin, George Emile and 13 more

Registry-linked trialOpen access · goldAbstract readMulticenter Study
In one paragraph

Article in The oncologist, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03275311 (Epidemiological Strategy and Medical Economic), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 23% 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.

NCT03275311 recruitingnot on this map

Epidemiological Strategy and Medical Economic (ESME) Research Program / Academic Real World Database: Evolution of the Therapeutic Care in Metastatic Breast Cancer Across the French Comprehensive Cancer Centers From 2008

TypeobservationalSponsorUNICANCERRan2014 to 2027Enrolled42,000ConditionsMetastatic Breast Cancer
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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

23 authors at 19 institutions in 1 country.

Fanny Le DuDepartment of Medical Oncology, Centre Eugène Marquis, Rennes, France.ORCID 0000-0002-4372-5832
Matthieu CartonDepartment of Biostatistics, Institut Curie, Saint-Cloud, France.
Thomas BachelotDepartment of Medical Oncology, Centre Léon-Bérard, Lyon, France.
Mahasti SaghatchianDepartment of Medical Oncology, Hôpital Américain, Paris, France.
Barbara PistilliDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Etienne BrainDepartment of Medical Oncology, Institut Curie/Saint Cloud, Paris, France.
Delphine LoiratDepartment of Biostatistics, Institut Curie, Saint-Cloud, France.
Laurence VanlemmensDepartment of Medical Oncology, Centre Oscar Lambret, Lille, France.
Thomas VermeulinCentre Henri Becquerel, Rouen, France.
George EmileDepartment of Medical Oncology, Centre François Baclesse, Caen, France.
Anthony GonçalvesDepartment of Medical Oncology, Institut Paoli-Calmettes, Marseille, France.
Mony UngDepartment of Medical Oncology, Institut Claudius Regaud, IUCT-Oncopole, CRCT, Inserm, Toulouse, France.
Marie RobertDepartment of Medical Oncology, Institut de Cancérologie de l'Ouest - René Gauducheau, Saint-Herblain, France.
Anne JaffreAnne jaffré Department of Medical Information, Institut Bergonié, Bordeaux, France.
Isabelle DesmoulinsDepartment of Medical Oncology, Centre Jean-Francois Leclerc, Dijon, France.
Christelle JouannaudDepartment of Medical Oncology, Institut Godinot, Reims, France.
Lionel UwerInstitut de Cancérologie de Lorraine, Nancy, France.
Jean Marc FerreroDepartment of Medical Oncology, Centre Antoine Lacassagne, Nice, France.
Marie-Ange Mouret-ReynierDepartment of Medical Oncology, Clermont-Ferrand, France.
William JacotDepartment of Medical Oncology, Institut du cancer de Montpellier, Montpellier, France.
Michaël ChevrotHealth Data and Partnership Department, Unicancer, Paris, France.
Suzette DelalogeDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Véronique DiérasDepartment of Medical Oncology, Centre Eugène Marquis, Rennes, France.ORCID 0000-0001-8094-4738
Institut Curie · FRCentre Eugène Marquis · FRInstitut Gustave Roussy · FRCentre Antoine Lacassagne · FRCentre François Baclesse · FRCentre Georges François Leclerc · FRCentre Henri BecquerelCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Léon Bérard · FRCentre Oscar Lambret · FRHôpital américain de paris · FRInserm · FRInstitut Bergonié · FRInstitut de Cancérologie de Lorraine · FRInstitut de Cancérologie de l'Ouest · FRInstitut de Recherche en Cancérologie de Montpellier · FRInstitut Jean Godinot · FRInstitut Paoli-Calmettes · FRUniCancer Group · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough adjuvant cancer treatments increase cure rates, they may induce clonal selection and tumor resistance. Information still lacks as whether (neo)adjuvant anti-HER2 treatments impact the patterns of recurrence and outcomes of HER2-positive (HER2+) metastatic breast cancer (MBC). We aimed to assess this in the large multicenter ESME real-world database. PATIENTS AND

methodsWe examined the characteristics and outcomes (overall survival (OS) and progression-free survival under first-line treatment (PFS1)) of HER2+ patients with MBC from the French ESME program with recurrent disease, as a function of the previous receipt of adjuvant trastuzumab. Multivariable analyses used Cox models adjusted for baseline demographic, prognostic factors, adjuvant treatment received, and disease-free interval.

resultsTwo thousand one hundred and forty-three patients who entered the ESME cohort between 2008 and 2017 had a recurrent HER2+ MBC. Among them, 56% had received (neo)adjuvant trastuzumab and 2.5% another anti-HER2 in this setting. Patients pre-exposed to trastuzumab were younger, had a lower disease-free interval, more HR-negative disease and more metastatic sites. While the crude median OS appeared inferior in patients exposed to adjuvant trastuzumab, as compared to those who did not (37.2 (95%CI 34.4-40.3) versus 53.5 months (95% CI: 47.6-60.1)), this difference disappeared in the multivariable model (HR = 1.05, 95%CI 0.91-1.22). The same figures were observed for PFS1.

conclusionsAmong patients with relapsed HER2+ MBC, the receipt of adjuvant trastuzumab did not independently predict for worse outcomes when adjusted to other prognostic factors.

Indexed as

Breast NeoplasmsChemotherapy, AdjuvantErb-b2 Receptor Tyrosine KinasesTrastuzumabAntineoplastic Combined Chemotherapy ProtocolsDisease-Free SurvivalFemaleHumansProgression-Free SurvivalErb-b2 Receptor Tyrosine KinasesTrastuzumabanti-HER2-targeted agentsbreast cancerde novo metastaticHER2 positivepertuzumabtrastuzumab

Identifiers

PMID37589218
PMCPMC10546827
OpenAlexW4385897980

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.