BACKGROUND: Resistance to endocrine therapies in hormone receptor-positive breast cancer is challenging. We aimed to assess the next-generation oral selective oestrogen receptor degrader (SERD) and complete oestrogen receptor antagonist, camizestrant, versus the first-approved SERD, fulvestrant, in post-menopausal women with oestrogen receptor-positive, HER2-negative, advanced breast cancer. METHODS: SERENA-2 is an open-label, randomised, phase 2 trial that is being conducted at 74 study centres across Asia, Europe, the Middle East, and North America. Female patients aged 18 years or older who were post-menopausal with histologically or cytologically confirmed metastastic or locoregional oestrogen receptor-positive, HER2-negative breast cancer, an Eastern Cooperative Oncology Group or WHO performance status of 0 or 1, and disease recurrence or progression on at least one line of endocrine therapy, and no more than one previous endocrine therapy in the advanced setting. Patients were initially randomly assigned (1:1:1:1) to receive oral camizestrant once daily at 75 mg, 150 mg, or 300 mg (until the 300 mg group was closed), or fulvestrant intramuscularly at 500 mg (per label). Randomisation was managed through an interactive web-based system and stratified by previous treatment with CDK4/6 inhibitors and presence of liver and/or lung metastases. The primary objective was to determine clinical efficacy of camizestrant versus fulvestrant at each dose level using the primary endpoint of investigator-assessed progression-free survival, per Response Evaluation Criteria in Solid Tumours (version 1.1), assessed by intention to treat in all randomly assigned patients (full analysis set). No formal statistical comparison for the efficacy analysis of the camizestrant 300 mg dose versus fulvestrant was to be performed. Safety analyses included all randomly assigned patients who received at least one dose of study treatment. This study is registered with ClinicalTrials.gov, NCT04214288, and is ongoing. FINDINGS: Between May 11, 2020, and Aug 10, 2021, 240 patients were randomly assigned to receive camizestrant 75 mg (n=74), 150 mg (n=73), 300 mg (n=20), or fulvestrant (n=73), and were included in the full analysis set. All patients received at least one dose of study drug. Median follow-up was 16·6 months (IQR 12·9-19·4) for the camizestrant 75 mg group, 16·3 months (12·9-18·3) for the camizestrant 150 mg group, and 14·7 months (12·7-20·1) for the fulvestrant 500 mg group. Median progression-free survival was 7·2 months (90% CI 3·7-10·9) with camizestrant 75 mg, 7·7 months (5·5-12·9) with camizestrant 150 mg, and 3·7 months (2·0-6·0) with fulvestrant. The hazard ratio for camizestrant 75 mg versus fulvestrant was 0·59 (90% CI 0·42-0·82; p=0·017), and the hazard ratio for camizestrant 150 mg versus fulvestrant was 0·64 (0·46-0·89; p=0·0090). Treatment-related adverse events occurred in 39 (53%) of 74 patients in the camizestrant 75 mg group, 49 (67%) of 73 patients in the camizestrant 150 mg group, 14 (70%) of 20 patients in the camizestrant 300 mg group, and 13 (18%) of 73 patients in the fulvestrant group. No single grade 3 or worse treatment-emergent adverse event occurred in more than two (3%) patients in any group. Serious treatment-emergent adverse events occurred in six (8%) patients in the camizestrant 75 mg group, seven (10%) patients in the camizestrant 150 mg group, two (10%) patients in the camizestrant 300 mg group, and four (5%) patients in the fulvestrant group. No treatment-related deaths occurred. INTERPRETATION: Camizestrant at 75 and 150 mg showed a significant benefit in progression-free survival versus fulvestrant. These results support further development of camizestrant for the treatment of oestrogen receptor-positive, HER2-negative breast cancer. FUNDING: AstraZeneca.

AV Medical Group St Petersburg Russia

Center of Oncoradiology Bács Kiskun County Teaching Hospital Kecskemét Hungary

Central City Hospital Uzhgorod National University Uzhgorod Ukraine

Centre Hospitalier de l'Ardenne Site de Libramont Libramont Chevigny Belgium

Department of Medical Oncology Ghent University Hospital Ghent Belgium

Helsicore Israeli Georgian Medical Research Clinic Tbilisi Georgia

IRCCS Azienda Ospedaliero universitaria di Bologna Bologna Italy

Late Development Oncology R and D AstraZeneca Cambridge UK

Makiivka City Hospital of Donetsk Region Makiivka Ukraine

Medical Center Verum Kyiv Ukraine

Medical Oncology Department Vall d'Hebron University Hospital and Breast Cancer Group Vall d'Hebron Institute of Oncology Barcelona Spain

Multidisciplinary Breast Center University Hospitals Leuven Campus Gasthuisberg Leuven Belgium

Oncology and Hematology Department Academician Fridon Todua Medical Center Research Institute of Clinical Medicine Tbilisi Georgia

Oncology Patient Safety Oncology R and D AstraZeneca Cambridge UK

Parexel International Bloemfontein South Africa

Parexel International Prague Czech Republic

Pyatigorsky Oncology Dispensary Pyatigorsk Russia

Republican Clinical Oncology Dispensary of the Ministry of Health of the Republic of Tatarstan Kazan Russia

Research and Early Development Oncology R and D AstraZeneca Cambridge UK

Sarah Cannon Research Institute Nashville TN USA

The Institute of Clinical Oncology Tbilisi Georgia

The Maria Sklodowska Curie Memorial Cancer Center and Institute of Oncology Warsaw Poland

Lancet Oncol. 2025 Mar;26(3):e127. doi: 10.1016/S1470-2045(25)00036-1. PubMed

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ClinicalTrials.gov
NCT04214288