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Abstract
This phase 3b/4 DESTINY-Breast12 study investigated trastuzumab deruxtecan (T-DXd) in patients with HER2+ metastatic breast cancer (mBC), with (n=263) and without (n=241) brain metastases (BMs). Patients received T-DXd (5.4 mg/kg). Primary endpoints were progression-free survival (PFS; BMs cohort) and objective response rate (ORR; non-BMs cohort). In the BMs cohort, 12-month PFS was 61.6%, and 12-month CNS PFS was 58.9%. In the non-BMs cohort, ORR was 62.7%. Grade 3 or higher adverse events occurred in ~50% of patients. These data show substantial and durable overall and intracranial activity for T-DXd, supporting its use in previously treated HER2+ mBC patients regardless of BMs status.
Publisher
Nature Medicine
Published On
Sep 13, 2024
Authors
Nadia Harbeck, Eva Ciruelos, Guy Jerusalem, Volkmar Müller, Naoki Niikura, Giuseppe Viale, Rupert Bartsch, Christian Kurzeder, Michaela J. Higgins, Roisin M. Connolly, Sally Baron-Hay, María Gión, Valentina Guarneri, Giampaolo Bianchini, Hans Wildiers, Santiago Escrivá-de-Romaní, Manoj Prahladan, Helen Bridge, Nataliya Kuptsova-Clarkson, Nana Scotto, Sunil Verma, Nancy U. Lin, the DESTINY-Breast12 study group
Tags
trastuzumab deruxtecan
HER2+ metastatic breast cancer
brain metastases
progression-free survival
response rate
adverse events
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