Trastuzumab Deruxtecan after Endocrine Therapy in Metastatic Breast Cancer

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • the DESTINY-Breast06 Trial Investigators - (Autor:in)
  • University of California at Los Angeles
  • Massachusetts General Hospital
  • Fudan University
  • National Cancer Centre
  • National Cancer Center Japan
  • The Latin American Cooperative Oncology Group
  • Baylor University Medical Center at Dallas
  • KU Leuven
  • Université Paris Cité
  • Harbin Medical University
  • Vall d'Hebron Institute of Oncology (VHIO)
  • Ospedale di Prato Santo Stefano
  • Yonsei University
  • Seoul National University
  • Centre Georges-François Leclerc
  • Université de Montpellier
  • AstraZeneca
  • Università degli Studi di Milano

Abstract

Background Outcomes in patients with hormone receptor-positive metastatic breast cancer worsen after one or more lines of endocrine-based therapy. Trastuzumab deruxtecan has shown efficacy in patients with metastatic breast cancer with low expression of human epidermal growth factor receptor 2 (HER2) after previous chemotherapy. Methods We conducted a phase 3, multicenter, open-label trial involving patients with hormone receptor-positive metastatic breast cancer with low HER2 expression (a score of 1+ or 2+ on immunohistochemical [IHC] analysis and negative results on in situ hybridization) or ultralow HER2 expression (IHC 0 with membrane staining) who had received one or more lines of endocrine-based therapy and no previous chemotherapy for metastatic breast cancer. Patients were randomly assigned in a 1:1 ratio to receive trastuzumab deruxtecan or the physician's choice of chemotherapy. The primary end point was progression-free survival (according to blinded independent central review) among the patients with HER2-low disease. Secondary end points included progression-free survival among all the patients who had undergone randomization, overall survival, and safety. Results Of the 866 patients who underwent randomization, 713 had HER2-low disease, and 153 had HER2-ultralow disease. Among the patients with HER2-low disease, the median progression-free survival was 13.2 months (95% confidence interval [CI], 11.4 to 15.2) in the trastuzumab deruxtecan group and 8.1 months (95% CI, 7.0 to 9.0) in the chemotherapy group (hazard ratio for disease progression or death, 0.62; 95% CI, 0.52 to 0.75; P<0.001); the results were consistent in the exploratory HER2-ultralow population. Data for overall survival were immature. Adverse events of grade 3 or higher occurred in 52.8% of the patients in the trastuzumab deruxtecan group and in 44.4% of those in the chemotherapy group. Adjudicated interstitial lung disease or pneumonitis occurred in 49 patients (11.3%; three events were grade 5 in severity) and in 1 patient (0.2%; grade 2), respectively. Conclusions Among patients with hormone receptor-positive, HER2-low or HER2-ultralow metastatic breast cancer who had received one or more lines of endocrine-based therapy, treatment with trastuzumab deruxtecan resulted in longer progression-free survival than chemotherapy. No new safety signals were identified.

Details

OriginalspracheEnglisch
Seiten (von - bis)2110-2122
Seitenumfang13
FachzeitschriftNew England Journal of Medicine
Jahrgang391
Ausgabenummer22
PublikationsstatusVeröffentlicht - 5 Dez. 2024
Peer-Review-StatusJa
Extern publiziertJa

Externe IDs

PubMed 39282896

Schlagworte

Ziele für nachhaltige Entwicklung

ASJC Scopus Sachgebiete

Schlagwörter

  • Breast Cancer, Hematology/Oncology, Treatments in Oncology