FINAL outcome ANALYSIS FROM THE PHASE II TUXEDO-1 TRIAL OF TRASTUZUMAB-DERUXTECAN IN HER2-positive breast cancer PATIENTS WITH active brain metastases.

Brain metastases HER2-positive breast cancer trastuzumab deruxtecan

Journal

Neuro-oncology
ISSN: 1523-5866
Titre abrégé: Neuro Oncol
Pays: England
ID NLM: 100887420

Informations de publication

Date de publication:
04 Jul 2024
Historique:
received: 02 04 2024
medline: 4 7 2024
pubmed: 4 7 2024
entrez: 4 7 2024
Statut: aheadofprint

Résumé

Brain metastases (BM) are a devastating complication of HER2-positive metastatic breast cancer (BC) and treatment strategies providing optimized local and systemic disease control are urgently required. The antibody-drug conjugate (ADC) trastuzumab deruxtecan (T-DXd) improved progression-free survival (PFS) and overall survival (OS) over trastuzumab emtansine but data regarding intracranial activity is limited. In the primary outcome analysis of TUXEDO-1, a high intracranial response rate (RR) was reported with T-DXd. Here, we report final PFS and OS results. TUXEDO-1 accrued adult patients with HER2-positive BC and active BM (newly diagnosed or progressing) without indication for immediate local therapy. The primary endpoint was intracranial RR; secondary endpoints included PFS, OS, safety, quality-of-life (QoL), and neurocognitive function. PFS and OS were estimated with the Kaplan-Meier method and analysed in the per-protocol population. At 26.5 months median follow-up, median PFS was 21 months (95% CI 13.3-n.r.) and median OS was not reached (95% CI 22.2-n.r.). With longer follow-up, no new safety signals were observed. The most common grade 3 adverse event was fatigue (20%). Grade 2 interstitial lung disease and a grade 3 symptomatic drop of left-ventricular ejection fraction were observed in one patient each. QoL was maintained over the treatment period. T-DXd yielded prolonged intra- and extracranial disease control in patients with active HER2-positive BC BM in line with results from the pivotal trials. These results support the concept of ADCs as systemic therapy for active BM.

Sections du résumé

BACKGROUND BACKGROUND
Brain metastases (BM) are a devastating complication of HER2-positive metastatic breast cancer (BC) and treatment strategies providing optimized local and systemic disease control are urgently required. The antibody-drug conjugate (ADC) trastuzumab deruxtecan (T-DXd) improved progression-free survival (PFS) and overall survival (OS) over trastuzumab emtansine but data regarding intracranial activity is limited. In the primary outcome analysis of TUXEDO-1, a high intracranial response rate (RR) was reported with T-DXd. Here, we report final PFS and OS results.
PATIENTS AND METHODS METHODS
TUXEDO-1 accrued adult patients with HER2-positive BC and active BM (newly diagnosed or progressing) without indication for immediate local therapy. The primary endpoint was intracranial RR; secondary endpoints included PFS, OS, safety, quality-of-life (QoL), and neurocognitive function. PFS and OS were estimated with the Kaplan-Meier method and analysed in the per-protocol population.
RESULTS RESULTS
At 26.5 months median follow-up, median PFS was 21 months (95% CI 13.3-n.r.) and median OS was not reached (95% CI 22.2-n.r.). With longer follow-up, no new safety signals were observed. The most common grade 3 adverse event was fatigue (20%). Grade 2 interstitial lung disease and a grade 3 symptomatic drop of left-ventricular ejection fraction were observed in one patient each. QoL was maintained over the treatment period.
DISCUSSION CONCLUSIONS
T-DXd yielded prolonged intra- and extracranial disease control in patients with active HER2-positive BC BM in line with results from the pivotal trials. These results support the concept of ADCs as systemic therapy for active BM.

Identifiants

pubmed: 38963808
pii: 7706127
doi: 10.1093/neuonc/noae123
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the Society for Neuro-Oncology.

Auteurs

Rupert Bartsch (R)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Anna Sophie Berghoff (AS)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Julia Furtner (J)

Department of Radiology, Medical University of Vienna, Vienna, Austria.
Research Center for Medical Image Analysis and Artificial Intelligence (MIAAI), Faculty of Medicine and Dentistry, Danube Private University, Krems, Austria.

Maximilian Marhold (M)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Elisabeth Sophie Bergen (ES)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Sophie Roider-Schur (S)

Department of Oncology, St. Joseph's Hospital, Vienna, Austria.

Maximilian Johannes Mair (MJ)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Angelika Martina Starzer (AM)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Heidrun Forstner (H)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Beate Rottenmanner (B)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Marie-Bernadette Aretin (MB)

Hospital Pharmacy, Vienna General Hospital and Medical University of Vienna, Vienna, Austria.

Karin Dieckmann (K)

Department of Radio-Oncology, Medical University of Vienna, Vienna, Austria.

Zsuzsanna Bago-Horvath (Z)

Department of Pathology, Medical University of Vienna, Vienna, Austria.

Helmuth Haslacher (H)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

Georg Widhalm (G)

Department of Neurosurgery, Medical University of Vienna, Vienna, Austria.

Aysegül Ilhan-Mutlu (A)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Christoph Minichsdorfer (C)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Thorsten Fuereder (T)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Thomas Szekeres (T)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

Leopold Oehler (L)

Research Center for Medical Image Analysis and Artificial Intelligence (MIAAI), Faculty of Medicine and Dentistry, Danube Private University, Krems, Austria.

Birgit Gruenberger (B)

Department of Oncology, LKH Wiener Neustadt, Wiener Neustadt, Austria.

Georg Pfeiler (G)

Department of Obstetrics and Gynaecology, Medical University of Vienna, Vienna, Austria.

Christian Singer (C)

Department of Obstetrics and Gynaecology, Medical University of Vienna, Vienna, Austria.

Ansgar Weltermann (A)

Department of Medicine 1, Elisabethinen Hospital Linz, Ordensklinikum Linz, Linz, Austria.

Luzia Berchtold (L)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.
Institute of Medical Statistics, Center for Medical Data Science, Medical University of Vienna, Vienna, Austria.

Matthias Preusser (M)

Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.

Classifications MeSH