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Trastuzumab Deruxtecan in HER2-Positive Metastatic Breast Cancer Patients with Brain Metastases: A DESTINY-Breast01 Subgroup Analysis

  • Guy Jerusalem
  • , Yeon Hee Park
  • , Toshinari Yamashita
  • , Sara A. Hurvitz
  • , Shanu Modi
  • , Fabrice Andre
  • , Ian E. Krop
  • , Xavier Gonzàlez Farré
  • , Benoit You
  • , Cristina Saura
  • , Sung Bae Kim
  • , Cynthia R. Osborne
  • , Rashmi K. Murthy
  • , Lorenzo Gianni
  • , Toshimi Takano
  • , Yali Liu
  • , Jillian Cathcart
  • , Caleb Lee
  • , Christophe Perrin
  • University of Liege
  • Kanagawa Cancer Center Research Institute
  • University of California at Los Angeles
  • Memorial Sloan-Kettering Cancer Center
  • Gustave Roussy
  • Yale University
  • Hospital General de Catalunya
  • Universite Claude Bernard Lyon 1
  • Vall d'Hebron Institute of Oncology
  • University of Ulsan
  • McKesson Specialty Health
  • Texas Oncology
  • University of Texas MD Anderson Cancer Center
  • Infermi Hospital
  • Japanese Foundation for Cancer Research
  • Daiichi Sankyo Company, Limited
  • Centre Georges-François Leclerc

Research output: Contribution to journal › Article › peer-review

Abstract

DESTINY-Breast01 (NCT03248492) evaluated trastuzumab deruxtecan (T-DXd; DS-8201) in patients with heavily pretreated HER2-positive metastatic breast cancer (mBC). We present a subgroup of 24 patients with a history of treated brain metastases (BM), a population with limited treatment options. In patients with BMs, the confirmed objective response rate (cORR) was 58.3% [95% confidence interval (CI), 36.6%–77.9%], and the median progression-free survival (mPFS) was 18.1 months (95% CI, 6.7–18.1 months). In patients without BMs (n = 160), cORR was 61.3% and mPFS was 16.4 months. Eight patients (47.1%) experienced a best overall intracranial response of partial response or complete response. Seven patients (41.2%) had a best percentage change in brain lesion diameter from baseline consistent with stable disease. Two patients (8.3%) with BMs and two (1.3%) without BMs experienced progression in the brain. The safety profile of T-DXd was consistent with previous studies. The durable clinical activity of T-DXd in this population warrants further investigation.

Original languageEnglish
Pages (from-to)2754-2762
Number of pages9
JournalCancer Discovery
Volume12
Issue number12
DOIs
StatePublished - 1 Dec 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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