Evidence map›Paper›PMID 41806276›Full record

ArticleAdvances in therapy2026

Treatment Patterns and Clinical Outcomes in Metastatic HR+/HER2- and Triple-Negative Breast Cancer in Canada: The HER2- TRENDS Study.

Karen Gambaro, Kahina Rachedi, Mark Basik, Gerald Batist, Fred Saad, Saima Hassan, Anne-Marie Mes-Masson, Dominique Boudreau, Francois Vincent, Eve St-Hilaire and 10 more

Abstract read
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In one paragraph

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

Karen GambaroCanadian National Centres of Excellence-Exactis Innovation, Montréal, QC, Canada.ORCID http://orcid.org/0000-0001-6712-5666
Kahina RachediCanadian National Centres of Excellence-Exactis Innovation, Montréal, QC, Canada.
Mark BasikSegal Cancer Centre-Jewish General Hospital, Montréal, QC, Canada.ORCID http://orcid.org/0000-0002-2633-5410
Gerald BatistSegal Cancer Centre-Jewish General Hospital, Montréal, QC, Canada.ORCID http://orcid.org/0000-0001-5430-3750
Fred SaadCentre de Recherche du Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada.ORCID http://orcid.org/0000-0003-2986-5617
Saima HassanCentre de Recherche du Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada.ORCID http://orcid.org/0000-0003-0232-2807
Anne-Marie Mes-MassonCentre de Recherche du Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada.ORCID http://orcid.org/0000-0002-6498-266X
Dominique BoudreauHôpital St-Sacrement, Québec, QC, Canada.ORCID http://orcid.org/0009-0004-7422-6659
Francois VincentCentre Hospitalier Régional de Trois-Riviéres, Trois-Rivières, QC, Canada.ORCID http://orcid.org/0000-0001-5159-4417
Eve St-HilaireCentre Hospitalier Universitaire Dr. Georges-L.-Dumont, Moncton, NB, Canada.
Helen MackayOdette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, ON, Canada.
Mahmoud AbdelsalamHorizon Health Network-The Moncton Hospital, Moncton, NB, Canada.ORCID http://orcid.org/0009-0002-4971-5181
Steven M YipArthur J.E. Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada.
Robert HanelCentre Hospitalier Universitaire de Sherbrooke, Sherbrooke, QC, Canada.
Simran ShokarAstraZeneca Canada, 1004 Middlegate Road, Suite 5000, Mississauga, ON, L4Y 1M4, Canada.
Zhor Senhaji MouhriAstraZeneca Canada, 1004 Middlegate Road, Suite 5000, Mississauga, ON, L4Y 1M4, Canada.
Matthew BadinAstraZeneca Canada, 1004 Middlegate Road, Suite 5000, Mississauga, ON, L4Y 1M4, Canada.ORCID http://orcid.org/0000-0002-5904-1128
Kristoph Klein-PannetonAstraZeneca Canada, 1004 Middlegate Road, Suite 5000, Mississauga, ON, L4Y 1M4, Canada. kristoph.klein-panneton@astrazeneca.com.
Arif Ali AwanThe Ottawa Hospital, Ottawa, ON, Canada.ORCID http://orcid.org/0000-0002-8552-6831
Maud MarquesCanadian National Centres of Excellence-Exactis Innovation, Montréal, QC, Canada.ORCID http://orcid.org/0009-0007-2032-7923

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe treatment landscape for human epidermal growth factor receptor 2-negative (HER2-) metastatic breast cancer (mBC) in Canada is rapidly evolving. This retrospective cohort study described real-world historical treatment patterns and clinical outcomes for patients with HER2- mBC.

methodsAdults enrolled in the pan-Canadian 'Personalize My Treatment' cancer registry and diagnosed with stage IV HER2- mBC (01/01/2015-03/01/2022) were eligible and followed until 03/01/2023. Hormone receptor-positive (HR+)/HER2- mBC and triple-negative mBC (mTNBC) were analyzed separately and further stratified by line of therapy. Main study outcomes included treatment patterns, PIK3CA/AKT1/PTEN alteration testing/positivity rates, and overall survival (OS), all analyzed descriptively.

resultsA total of 507 patients with HER2- mBC were included (HR+/HER2- mBC: 387; mTNBC: 120; median follow-up: 54.1 months). The most common HR+/HER2- mBC treatments were cyclin‑dependent kinase 4/6 inhibitors (CDK4/6is) plus endocrine therapy (ET) in first line (1L; 55.0%), targeted therapies (22.9%) and CDK4/6i + ET (22.0%) in second line (2L), and chemotherapy (CT) monotherapy (42.7%) in third line (3L). CT monotherapy was the most common mTNBC treatment in 1L (35.1%), 2L (50.6%), and 3L (54.8%). Attrition was similar for HR+/HER2- mBC and mTNBC from 1L-2L (16.9% and 16.3%, respectively) but was lower for HR+/HER2- mBC from 2L-3L (33.2% and 38.6%) and 3L-4L (48.1% and 62.1%). PIK3CA/AKT1/PTEN alteration testing was performed in 31.8% of patients with HR+/HER2- mBC and 50.0% with mTNBC, with alterations identified in 15.4% and 20.0% of patients, respectively. Median OS (65.9 and 31.4 months, respectively), OS rates (1 year: 94.8% and 79.8%; 5 years: 56.0% and 21.7%), and time to next treatment (1L-2L: 24.5 and 8.1 months; 2L-3L: 10.1 and 5.1 months) were greater for HR+/HER2- mBC than mTNBC.

conclusionsThese findings describe historical HER2- mBC treatment patterns and associated outcomes in Canada. Ongoing research is needed to optimize therapeutic strategies, expand novel treatment access, and improve patient outcomes.

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesTriple Negative Breast NeoplasmsAdultAgedAntineoplastic Combined Chemotherapy ProtocolsCanadaFemaleHumansMiddle AgedNeoplasm MetastasisReceptors, EstrogenReceptors, ProgesteroneRetrospective StudiesTreatment OutcomeERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneBreast cancerHormone receptorHuman epidermal growth factor receptor 2Overall survivalReal-world evidenceTreatment patternsTriple negative

Identifiers

PMID41806276

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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.