Trastuzumab deruxtecan in HER2-positive breast cancer with brain metastases: a single-arm, phase 2 trial

Rupert Bartsch(Medical University of Vienna), Anna S. Berghoff(Medical University of Vienna), Julia Furtner(Medical University of Vienna), Maximilian Marhold(Medical University of Vienna), Elisabeth Bergen(Medical University of Vienna), Sophie Roider‐Schur, Angelika M. Starzer(Medical University of Vienna), Heidrun Forstner(Medical University of Vienna), Beate Rottenmanner(Medical University of Vienna), Karin Dieckmann(Medical University of Vienna), Zsuzsanna Bagó-Horváth(Medical University of Vienna), Helmuth Haslacher(Medical University of Vienna), Georg Widhalm(Medical University of Vienna), Aysegül Ilhan‐Mutlu(Medical University of Vienna), Christoph Minichsdorfer(Medical University of Vienna), Thorsten Fuereder(Medical University of Vienna), Thomas Szekeres(Medical University of Vienna), Leopold Oehler, Birgit Gruenberger(Fachhochschule Wiener Neustadt), Christian F. Singer(Medical University of Vienna), Ansgar Weltermann(Krankenhaus der Elisabethinen), Rainer Puhr(Medical University of Vienna), Matthias Preusser(Medical University of Vienna)
Nature Medicine
August 8, 2022
Cited by 387Open Access
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Abstract

Trastuzumab deruxtecan is an antibody-drug conjugate with high extracranial activity in human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer. We conducted the prospective, open-label, single-arm, phase 2 TUXEDO-1 trial. We enrolled patients aged ≥18 years with HER2-positive breast cancer and newly diagnosed untreated brain metastases or brain metastases progressing after previous local therapy, previous exposure to trastuzumab and pertuzumab and no indication for immediate local therapy. Patients received trastuzumab deruxtecan intravenously at the standard dose of 5.4 mg per kg bodyweight once every 3 weeks. The primary endpoint was intracranial response rate measured according to the response assessment in neuro-oncology brain metastases criteria. A Simon two-stage design was used to compare a null hypothesis of <26% response rate against an alternative of 61%. Fifteen patients were enrolled in the intention-to-treat population of patients who received at least one dose of study drug. Two patients (13.3%) had a complete intracranial response, nine (60%) had a partial intracranial response and three (20%) had stable disease as the best intracranial response, with a best overall intracranial response rate of 73.3% (95% confidential interval 48.1-89.1%), thus meeting the predefined primary outcome. No new safety signals were observed and global quality-of-life and cognitive functioning were maintained over the treatment duration. In the TUXEDO-1 trial (NCT04752059, EudraCT 2020-000981-41), trastuzumab deruxtecan showed a high intracranial response rate in patients with active brain metastases from HER2-positive breast cancer and should be considered as a treatment option in this setting.


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