Pharmacodynamics of Camizestrant Treatment in Postmenopausal Women With Estrogen Receptor–Positive, Human Epidermal Growth Factor Receptor 2–Negative Primary Breast Cancer: Results From the Randomized, Presurgical SERENA-3 Study

SERENA-3 demonstrates that camizestrant 75 mg once daily (Phase III dose) is well-tolerated and achieves maximal reduction in ER through known mechanisms, that is, antagonism and degradation, by 5-7 days, and proliferation suppression determined by Ki67 expression, by 12-15 days. These data support camizestrant 75 mg once daily as the preferred dose for ongoing clinical development and highlight the importance of presurgical WOO studies in guiding dose selection.

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Publication Details

Journal
Journal of Clinical Oncology
Published
2026-01-16
DOI
https://doi.org/10.1200/jco-25-01548
Primary Topic
Estrogen and related hormone effects
Type
article
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article

Pharmacodynamics of Camizestrant Treatment in Postmenopausal Women With Estrogen Receptor–Positive, Human Epidermal Growth Factor Receptor 2–Negative Primary Breast Cancer: Results From the Randomized, Presurgical SERENA-3 Study

Myria Nikolaou, Ekaterine Arkania, Andy Sykes, Cheung KL et al.
Journal of Clinical Oncology
Estrogen and related hormone effects
article

Pharmacodynamics of Camizestrant Treatment in Postmenopausal Women With Estrogen Receptor–Positive, Human Epidermal Growth Factor Receptor 2–Negative Primary Breast Cancer: Results From the Randomized, Presurgical SERENA-3 Study

Myria Nikolaou, Ekaterine Arkania, Andy Sykes, Cheung KL, Alastair Mathewson, Teresa Klinowska, Iain Moppett, Christopher J. Morrow, Justin P.O. Lindemann, Zaza Katashvili, Teimuraz Gogitidze, Gia Nemsadze, Giorgi Dzagnidze, Maxine Ajimi, Juan Enrique Bargalló Rocha, John F.R. Robertson, Maurizio Scaltriti
article en

Abstract

SERENA-3 demonstrates that camizestrant 75 mg once daily (Phase III dose) is well-tolerated and achieves maximal reduction in ER through known mechanisms, that is, antagonism and degradation, by 5-7 days, and proliferation suppression determined by Ki67 expression, by 12-15 days. These data support camizestrant 75 mg once daily as the preferred dose for ongoing clinical development and highlight the importance of presurgical WOO studies in guiding dose selection.

Journal of Clinical OncologyVol. 44(9)
Batumi Shota Rustaveli State University (GE), University of Nottingham (GB), Royal Derby Hospital (GB), AstraZeneca (South Korea) (KR), AstraZeneca (Netherlands) (NL), AstraZeneca (Singapore) (SG), AstraZeneca (Poland) (PL), David Tvildiani Medical University (GE), AstraZeneca (Spain) (ES), Instituto Nacional de Cancerología (MX), Batumi Independent University (GE), Tbilisi State Medical University (GE)
Good health and well-being
Openalex Percentile: Top 88%
Estrogen and related hormone effects
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