Evidence map›Paper›PMID 36520434›Full record

ArticleJAMA network open2022

Association of Endocrine Therapy for HR+/ERBB2+ Metastatic Breast Cancer With Survival Outcomes.

Marcela Carausu, Matthieu Carton, Véronique Diéras, Thierry Petit, Séverine Guiu, Anthony Gonçalves, Paule Augereau, Jean Marc Ferrero, Christelle Levy, Mony Ung and 8 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in JAMA network open, 2022. 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

18 authors at 15 institutions in 1 country.

Marcela CarausuDepartment of Medical Oncology, Institut Curie, Saint-Cloud, France.
Matthieu CartonDepartment of Biostatistics, Institut Curie, Saint-Cloud, France.
Véronique DiérasDepartment of Medical Oncology, Centre Eugène Marquis, Rennes, France.
Thierry PetitDepartment of Medical Oncology, Centre Paul Strauss/ICANS, Strasbourg, France.
Séverine GuiuDepartment of Medical Oncology, Institut régional du Cancer Montpellier, France.
Anthony GonçalvesDepartment of Medical Oncology, Institut Paoli-Calmettes, Marseille, France.
Paule AugereauDepartment of Medical Oncology, Institut de Cancérologie de l'Ouest, Angers, France.
Jean Marc FerreroDepartment of Medical Oncology, Centre Antoine Lacassagne, Nice, France.
Christelle LevyDepartment of Medical Oncology, Centre François Baclesse, Caen, France.
Mony UngDepartment of Medical Oncology, Institut Claudius Regaud, Toulouse, France.
Isabelle DesmoulinsDepartment of Medical Oncology, Centre Georges-François Leclerc, Dijon, France.
Marc DebledDepartment of Medical Oncology, Institut Bergonié, Bordeaux, France.
Thomas BachelotDepartment of Medical Oncology, Centre Léon Bérard, Lyon, France.
Barbara PistilliDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Jean-Sébastien FrenelDepartment of Medical Oncology, Institut de cancérologie de l'Ouest, Nantes, France.
Audrey MailliezDepartment of Medical Oncology, Centre Oscar Lambret, Lille, France.
Michaël ChevrotHealth Data and Partnership Department, Unicancer, Paris, France.
Luc CabelDepartment of Medical Oncology, Institut Curie, Saint-Cloud, France.
Institut Curie · FRInstitut de Cancérologie de l'Ouest · FRCentre Antoine Lacassagne · FRCentre Eugène Marquis · FRCentre François Baclesse · FRCentre Georges François Leclerc · FRCentre Léon Bérard · FRCentre Oscar Lambret · FRInstitut Bergonié · FRInstitut Claudius Regaud · FRInstitut de Cancérologie Strasbourg · FRInstitut de Recherche en Cancérologie de Montpellier · FRInstitut Gustave Roussy · FRInstitut Paoli-Calmettes · FRUniCancer Group · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Evidence suggests that patients with human epidermal growth factor receptor 2-positive (ERBB2+ [formerly HER2+]) metastatic breast cancer (MBC) have different clinical characteristics and outcomes according to their hormone receptor (HR) status. The place of endocrine therapy (ET) for patients with HR+/ERBB2+ is still not clearly defined in this setting. Objective: To evaluate the association of HR status and first-line inclusion of ET with outcomes among patients with ERBB2+ MBC. Design, Setting, and Participants: This cohort study was an analysis of clinical data from the French clinical Epidemiological Strategy and Medical Economics (ESME) cohort, including patients with MBC who started treatment between 2008 and 2017. The last date of follow-up was June 18, 2020. Data were analyzed from May 2021 to May 2022. Exposures: Patients were treated with first-line ERBB2-targeted therapy and either chemotherapy (CT) with or without ET or ET alone. For the study of the association of maintenance ET with outcomes, we included patients treated with first-line ERBB2-targeted therapy with CT and with or without maintenance ET. Main Outcomes and Measures: Median overall survival (OS) and median first-line progression-free survival (PFS) were reported using the Kaplan-Meier method. Cox proportional hazards models and a propensity score were constructed to report and adjust for prognostic factors. Multivariable analysis included age at MBC, time to MBC, number of metastatic sites, type of metastases, and Eastern Cooperative Oncology Group performance status. Results: Among 4145 women with ERBB2+ MBC, 2696 patients had HR+ (median [IQR] age, 58.0 [47.0-67.0] years) and 1449 patients had HR- (56.0 [47.0-64.0] years) tumors. The median OS for patients with HR+ vs HR- tumors was 55.9 months (95% CI, 53.7-59.4 months) vs 42.0 months (95% CI, 38.8-45.2 months), confirmed in multivariable analysis (hazard ratio, 1.40; 95% CI, 1.26-1.56; P < .001). The median PFS for patients with HR+ vs HR- tumors was 12.2 months (95% CI, 11.5-12.9 months) vs 9.8 months (95% CI, 9.2-11.0 months; P = .01), and the HR was 1.15 (95% CI, 1.06-1.26; P < .001). In multivariable analysis, no significant difference was found in OS or PFS for 1520 patients treated with ERBB2-targeted therapy with CT and with or without ET vs 203 patients receiving ERBB2-targeted therapy with ET, regardless of type of ERBB2-targeted therapy (trastuzumab or trastuzumab with pertuzumab). This result was confirmed by matching patients using a propensity score. Using the time-dependent ET variable among patients with ERBB2-targeted therapy with CT, those with maintenance ET had significantly better PFS (hazard ratio, 0.70; 95% CI, 0.60-0.82; P < .001) and OS (hazard ratio, 0.47; 95% CI, 0.39-0.57; P < .001). Conclusions and Relevance: These results suggest that ET-containing first-line regimens may be associated with benefits among a subgroup of patients with HR+/ERBB2+ MBC.

Indexed as

Breast NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsCohort StudiesErb-b2 Receptor Tyrosine KinasesFemaleHumansMiddle AgedTrastuzumabERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesTrastuzumab

Identifiers

PMID36520434
PMCPMC9856509
OpenAlexW4311777021

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.