Observational studyBMC cancer2025
Abemaciclib in combination with endocrine therapy for the treatment of HR-positive/HER2-negative locally advanced/metastatic breast cancer in the UK: an observational study.
Observational study in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
The trial behind it
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Who cites it
1 citing paper in PubMed.
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Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundCyclin-dependent kinase 4/6 inhibitors combined with endocrine therapy are now standard of care in the first- or second-line settings for hormone receptor positive (HR+), human epidermal growth factor 2 negative (HER2-) patients with advanced / metastatic breast cancer (ABC/MBC). Abemaciclib was first authorised in the United Kingdom (UK) in 2018 via patient access schemes before approval for routine use. This study assessed the treatment patterns and outcomes of abemaciclib in combination with endocrine therapy in a real-world setting.
methodsThis was an observational, multi-centre retrospective chart review of women in the UK with HR+, HER2- ABC/MBC treated with abemaciclib plus endocrine therapy during 07/2021 to 05/2022 with [Formula: see text]3 months' follow-up data. Data were summarised using descriptive analyses. Kaplan-Meier methods estimated time to progression (TTP) with 95% confidence intervals (CIs).
resultsOne hundred seventy-four adult women from 9 institutions were included. Median patient age at abemaciclib initiation was 65.2 years. Best tumor response was recorded in 78.2% (n = 136) of patients; 0.7% had complete response, 27.9% had partial response, 59.6% had stable disease and 11.8% had disease progressed. Abemaciclib was associated with a 12-month TTP rate of 81.1% (first line), 68.2% (second line) and 58.2% (third line). The median TTP for patients who received abemaciclib in the first, second, and third line of treatment was: not reached, 27.7 months (95% CI: 11.7 months-not reached), and 19.3 months (95% CI: 7.7-21.9 months), respectively.
conclusionsThese findings support the benefit of abemaciclib in women with HR+, HER2- ABC/MBC in the real-world and complement data from MONARCH 2 and 3 clinical trials.
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