Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UC Irvine
Dates
study started
study ends around
Principal Investigator
by Ritesh Parajuli (uci)

Description

Summary

This study will look at the efficacy and safety of trastuzumab deruxtecan (T-DXd) in a neoadjuvant setting, in high-risk, HER2-positive early non-metastatic breast cancer.

Official Title

A Phase 3 Open-label Trial of Neoadjuvant Trastuzumab Deruxtecan (T-DXd) Monotherapy or T-DXd Followed by THP Compared to ddAC-THP in Participants With High-risk HER2-positive Early-stage Breast Cancer (DESTINY-Breast11)

Details

The target population of interest in this study is participants with high-risk HER2-positive early-stage breast cancer. The purpose of this study is to determine the efficacy and safety of T-DXd neoadjuvant therapy.

Participants will be randomised to one of 3 arms: T-DXd monotherapy (Arm A), T-DXd followed by THP (Arm B), or ddAC-THP (Arm C).

Keywords

Breast Neoplasms, Breast Cancer, HER2-positive Early Breast Cancer, Trastuzumab Trastuzumab Deruxtecan (T-DXd; DS-8201a), DESTINY-BREAST11, Receptor, ErbB-2, Antineoplastic Agents, Phytogenic, Antineoplastic Agents;Molecular Mechanisms of Pharmacological Action, DB11, Enhertu, HER2 (human epidermal growth factor receptor 2), trastuzumab deruxtecan, Paclitaxel, Trastuzumab, pertuzumab, Doxorubicin, Cyclophosphamide

Eligibility

You can join if…

Open to people ages 18 years and up

  • Patients must be at least 18 years of age.
  • Histologically documented HER2-positive early breast cancer (EBC) participants, including clinical stage at presentation (based on mammogram or breast MRI assessment): T0-4 (inclusive of inflammatory breast cancer), N1-3, M0 or ≥ T3, N0, M0 as determined by the AJCC staging system, 8th edition
  • ECOG performance status of 0 or 1 at randomization
  • Adequate organ and bone marrow function
  • LVEF ≥ 50% within 28 days before randomization
  • FFPE tissue block (2 cores) or 20 freshly-cut, serial tumor slides for HER2 assessment by central lab. If blocks are incomplete or fewer than 20 slides are available, participants may be eligible following discussion with the AstraZeneca Study Physician

You CAN'T join if...

  • prior history of invasive breast cancer
  • stage IV breast cancer (determined by AJCC staging system)
  • any primary malignancy within 3 years (except resected non-melanoma skin cancer, curatively treated in situ disease) Note: This includes a second current breast primary malignancy (ie, bilateral breast cancer)
  • history of DCIS (except those treated with mastectomy >5 years prior to current diagnosis)
  • History of, or current, ILD/pneumonitis
  • Prior systemic therapy for the treatment of breast cancer
  • Previous treatment with anthracyclines, cyclophosphamide or taxanes for any malignancy

Locations

  • Research Site
    Beverly Hills California 90211 United States
  • Research Site
    Orange California 92868 United States
  • Research Site
    Glendale California 91204 United States
  • Research Site
    Los Alamitos California 90720 United States

Lead Scientist at University of California Health

  • Ritesh Parajuli (uci)
    Associate Clinical Professor, Medicine, School of Medicine. Authored (or co-authored) 25 research publications

Details

Status
in progress, not accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
AstraZeneca
Links
Redacted SAP Redacted CSP Redacted CSR synopsis
ID
NCT05113251
Phase
Phase 3 research study
Study Type
Interventional
Participants
About 927 people participating
Last Updated