Evidence map›Paper›PMID 42474828›Full record

Observational studyBreast cancer research and treatment2026

Real-world treatment patterns and outcomes in hormone receptor-positive, HER2-low metastatic breast cancer, 2018-2023: a retrospective, observational, US cohort study.

Erica L Mayer, Simon M Collin, Sam Hillman, Luis C Berrocal-Almanza, Joseph Sparano, Clara Lam

Abstract readObservational Study
In one paragraph

Observational study in Breast cancer research and treatment, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Erica L MayerDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, US.
Simon M CollinOncology Outcomes Research, Oncology Business Unit, Evidence Generation to Publications (EG2P), AstraZeneca, Cambridge, UK. simon.collin@astrazeneca.com.ORCID http://orcid.org/0000-0002-1239-1681
Sam HillmanCenter of Oncology Data Excellence (CODE), Oncology Business Unit, Evidence Generation to Publications (EG2P), AstraZeneca, Cambridge, UK.
Luis C Berrocal-AlmanzaOncology Outcomes Research, Oncology Business Unit, Evidence Generation to Publications (EG2P), AstraZeneca, Cambridge, UK.
Joseph SparanoDivision of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, Tisch Cancer Institute, New York, NY, US.
Clara LamBreast Franchise, Medical Affairs, Oncology Business Unit, AstraZeneca, Gaithersburg, MD, US.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo investigate real-world demographics, clinical characteristics, treatment patterns, and outcomes in US patients with ≥ 1 line of therapy (LOT) for hormone receptor-positive (HR+) HER2-low metastatic breast cancer (mBC).

methodsThis retrospective cohort study used a US-based electronic health record-derived de-identified database of patients with mBC diagnosed in 2018-2023. Patient demographics, clinical characteristics at date of mBC diagnosis, treatment patterns, and real-world overall survival (rwOS) and progression-free survival (rwPFS) were analyzed.

resultsOf 2662 patients, 49.4% had recurrent mBC. The median (Q1-Q3) number of LOTs was 2 (1-3). Endocrine therapy (ET) plus a cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) was the most common first-line, second-line, and third-line therapy. In LOT1, 86.2% of patients received ET-containing regimens; consecutive use of ET-containing regimens in subsequent lines constituted 66.0%, 46.0%, 28.3%, and 19.3% of patients in LOT2-5, respectively. Of 830 patients who received chemotherapy, a median (Q1-Q3) of 1 (0-2) prior lines of ET-containing regimens were received. Median (95% CI) rwOS from mBC diagnosis was 42.4 (40.7, 45.0) months; 5-year survival was 36.9%. Median (95% CI) rwPFS decreased from 16.3 (15.2, 17.3) months in LOT1 to 9.1 (8.3, 10.0), 6.2 (5.6, 7.2), 5.3 (4.6, 6.1), and 3.8 (3.3, 4.9) months in LOT2-5, respectively.

conclusionsTreatment of HR+, HER2-low mBC was characterized by progressive endocrine exhaustion followed by later lines of chemotherapy, with outcomes worsening at each subsequent treatment line. Data highlight the need for new, effective treatment options in this setting.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesAdultAgedAged, 80 and overFemaleHumansMiddle AgedNeoplasm MetastasisReceptors, EstrogenReceptors, ProgesteroneRetrospective StudiesTreatment OutcomeUnited StatesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneHER2-lowHormone receptor–positiveMetastatic breast cancerReal-world evidence

Identifiers

PMID42474828
PMCPMC13385082

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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.