Abstract PS5-01-27: Outcomes by hormone receptor (HR) status in patients (pts) with HER2+ advanced/metastatic breast cancer (mBC) with brain metastases (BM) treated with trastuzumab deruxtecan (T-DXd): a post-hoc subgroup analysis of DESTINY-Breast12
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Abstract Background: T-DXd demonstrated substantial and durable overall and intracranial clinical activity in DESTINY-Breast12. In pts with BM, 12-month progression-free survival (PFS) and central nervous system (CNS) PFS rates were 61.6% and 58.9%, respectively, and CNS objective response rate (ORR) was 71.7% (79.2% in pts with stable and 62.3% in pts with active BM). In the cohort of pts without BM, efficacy of T-DXd was in line with previous data, and there were no new safety signals. To date, T-DXd has shown clinical benefit irrespective of HR status, most recently in first-line HER2+ mBC in DESTINY-Breast09. In a post-hoc analysis of DESTINY-Breast12, outcomes by HR status in pts with BM were explored. Methods: Pts ≥18 years old with HR-positive (HR+) or HR-negative (HR−) HER2+ mBC whose disease had progressed after ≤2 previous lines of therapy were eligible; BM were required to be stable or active (untreated/treated progressing) and not in need of immediate local therapy. All pts received intravenous T-DXd 5.4 mg/kg every 3 weeks. Efficacy outcomes were analyzed by baseline HR status using the Kaplan-Meier technique for PFS. Results: In total, 262 pts with baseline BM were included in this analysis, of whom 165 (63.0%) had HR+ disease. Among pts with BM, the median age (range) was 52.0 (30-80) years in the HR+ subgroup and 54.0 (28-86) years in the HR− subgroup (n=97). Median follow up for PFS at data cutoff (February 8, 2024) was 13.1 months in both subgroups. Median PFS was not calculable for either HR subgroup. The 12-month PFS and CNS PFS, as well as CNS ORR, were indicative of consistent responses with T-DXd regardless of HR subgroup; confirmed ORRs, including in pts with measurable disease at baseline, indicated activity of T-DXd in pts with HR+ and HR− tumors (Table). The median total treatment duration (range) was 12.0 (0.7-26.9) months in the HR+ subgroup and 11.1 (0.1-26.8) months in the HR− subgroup. Adverse events of any grade in pts occurred with a similar overall incidence in both HR subgroups; the most common Grade ≥3 events were neutropenia (12.1%), anemia (7.3%), and fatigue (6.7%) in the HR+ subgroup, and neutropenia (11.3%), decreased neutrophil count (8.2%), and anemia (7.2%) in the HR− subgroup. Interstitial lung disease / pneumonitis occurred in 26 (Grade 5, n=3) and 16 (Grade 5, n=3) pts in the HR+ and HR− subgroups, respectively. Results by HR subgroup in the cohort without BM (data not presented) were consistent with those from the cohort with BM. Conclusion: T-DXd demonstrated consistent intracranial activity and safety in pts with BM, regardless of HR status. These data reinforce the utility of T-DXd as a second-line treatment regardless of HR status in pts with HER2+ mBC. Citation Format: H. Wildiers, N. Harbeck, E. Ciruelos, G. Jerusalem, V. Müller, N. Niikura, G. Viale, R. Bartsch, C. Kurzeder, M. Higgins, R. Connolly, S. Baron-Hay, M. Gión, V. Guarneri, G. Bianchini, S. Escrivá-de-Romaní, M. Prahladan, S. Anand, N. Toms, R. Antony, N. Lin. Outcomes by hormone receptor (HR) status in patients (pts) with HER2+ advanced/metastatic breast cancer (mBC) with brain metastases (BM) treated with trastuzumab deruxtecan (T-DXd): a post-hoc subgroup analysis of DESTINY-Breast12 [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS5-01-27.
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Le contrôle bibliographique ouvert
DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.
- Titre Crossref
- Abstract PS5-01-27: Outcomes by hormone receptor (HR) status in patients (pts) with HER2+ advanced/metastatic breast cancer (mBC) with brain metastases (BM) treated with trastuzumab deruxtecan (T-DXd): a post-hoc subgroup analysis of DESTINY-Breast12
- Date Crossref
- 17/02/2026
- Éditeur
- American Association for Cancer Research (AACR)
- Type
- journal-article
Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.
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KU Leuven pays non établi dans la noticeUniversité ou école supérieure
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LMU Klinikum pays non établi dans la noticeÉtablissement de santé
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KU Leuven, LMU Klinikum et Ludwig-Maximilians-Universität München, avec 9 autres affiliations.
Une affiliation ne permet pas de déduire la nationalité d’un auteur.