DS-8201a Versus T-DM1 for Human Epidermal Growth Factor Receptor 2 (HER2)-Positive, Unresectable and/or Metastatic Breast Cancer Previously Treated With Trastuzumab and Taxane [DESTINY-Breast03]
Trastuzumab deruxtecan (T-DXd): T-DXd is sterile lyophilized powder reconstituted into a sterile aqueous solution (100 mg/5 mL) to be administered intravenously.
Ado-trastuzumab emtansine (T-DM1): The treatment will be in accordance with the approved label.
Study summary
This study is designed to compare the anti-tumor activity as well as the safety and efficacy of DS-8201a versus T-DM1 in HER2-positive, unresectable and/or metastatic breast cancer subjects previously treated with trastuzumab and taxane.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
1. Must be competent and able to comprehend, sign, and date an Institutional Review Board (IRB) or Ethics Committee (EC) approved ICF before performance of any study-specific procedures or tests.
2. Adults ≥18 y old. (Please follow local regulatory requirements if the legal age of consent for study participation is \>18 y old.)
3. Pathologically documented breast cancer that:
1. is unresectable or metastatic.
2. has confirmed HER2-positive expression as determined according to American Society of Clinical Oncology - College of American Pathologists guidelines evaluated at a central laboratory.23
3. was previously treated with trastuzumab and taxane in the advanced/ metastatic setting or progressed within 6 mo after neoadjuvant or adjuvant treatment involving a regimen including trastuzumab and taxane.
4. Documented radiologic progression (during or after most recent treatment or within 6 mo after completing adjuvant therapy).
5. Subjects must be HER2-positive as confirmed by central laboratory assessment of most recent tumor tissue sample available. If archived tissue is not available, a fresh biopsy is required.
6. Presence of at least 1 measurable lesion per modified Response Evaluation Criteria in Solid Tumors (mRECIST) version 1.1
Exclusion Criteria:
1. Prior treatment with an anti-HER2 ADC (such as T-DM1) in the metastatic setting. Prior treatment in the adjuvant/neoadjuvant setting would be allowed if progression of disease did not occur within 12 mo of end of adjuvant therapy.
2. Uncontrolled or significant cardiovascular disease, including any of the following:
1. History of myocardial infarction within 6 mo before randomization;
2. History of symptomatic congestive heart failure (New York Heart Association Class II to IV);
3. Troponin levels consistent with myocardial infarction as defined according to the manufacturer within 28 d prior to randomization;
4. Corrected QT interval (QTc) prolongation to \> 470 ms (females) or \>450 ms (male) based on average of Screening triplicate 12-lead ECG;
5. LVEF \< 50% within 28 d prior to randomization
3. Has a history of (noninfectious) ILD/pneumonitis that required steroids, has current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at Screening.
4. Spinal cord compression or clinically active central nervous system (CNS) metastases, defined as untreated or symptomatic, or requiring therapy with corticosteroids or anticonvulsants to control associated symptoms.
* Subjects with clinically inactive brain metastases may be included in the study.
* Subjects with treated brain metastases that are no longer symptomatic and who require no treatment with corticosteroids or anticonvulsants may be included in the study if they have recovered from the acute toxic effect of radiotherapy. A minimum of 2 wk must have elapsed between the end of whole brain radiotherapy and study enrollment.
5. Has a history of severe hypersensitivity reactions to either the drug substances or inactive ingredients in the drug product.
6. History of severe hypersensitivity reactions to other mAbs.
Primary outcome measure(s)
Progression-Free Survival (PFS) Based on Blinded Independent Central Review (BICR) in Participants With HER2-Positive, Unresectable and/or Metastatic Breast Cancer Previously Treated With Trastuzumab and Taxane — Up to 33 months (data cut-off) Progression-free survival (PFS) by BICR was defined as the time from the date of enrollment to the earlier of the dates of the first objective documentation of disease progression (as per RECIST v1.1) or death due to any cause. Progressive disease was defined as at least a 20% increase in the sum of diameters of target lesions.
Trial sites (164)
Facility
City
Region
Status
UCLA Hematology Oncology
Los Angeles
California
Sharp Memorial Hospital
San Diego
California
University of California San Francisco
San Francisco
California
Innovative Clinical Research Institute
Whittier
California
Washington Cancer Institute
Washington D.C.
District of Columbia
Florida Cancer Specialists-Broadway
Fort Myers
Florida
Florida Cancer Specialists NORTH
St. Petersburg
Florida
Piedmont Cancer Institute, PC
Atlanta
Georgia
Loyola University Health System
Maywood
Illinois
Norton Cancer Institute
Louisville
Kentucky
Dana-Farber Cancer Institute
Boston
Massachusetts
University of Nebraska Medical Center
Omaha
Nebraska
North Shore Hematology Oncology Associates, PC
East Setauket
New York
University of Rochester
Rochester
New York
Wake Forest University Baptist Medical Center
Winston-Salem
North Carolina
University of Cincinnati Medical Center
Cincinnati
Ohio
Seidman Cancer Center
Cleveland
Ohio
The Ohio State University
Columbus
Ohio
Dayton Physicians, LLC
Kettering
Ohio
Magee-Womens Hospital of UPMC
Pittsburgh
Pennsylvania
Tennessee Oncology- St Thomas Location
Nashville
Tennessee
Vanderbilt Breast Center at One Hundred Oaks
Nashville
Tennessee
UT Southwestern Medical Center
Dallas
Texas
Houston Methodist Hospital / Houston Methodist Cancer Center
Houston
Texas
MD Anderson Cancer Center
Houston
Texas
Millennium Oncology
Houston
Texas
The University of Texas Health Science Center at Tyler
Tyler
Texas
MultiCare Health System Institute for Research and Innovation
Auburn
Washington
The Tweed Hospital
Tweed Heads
New South Wales
Princess Alexandra Hospital
Woolloongabba
Queensland
Box Hill Hospital
Box Hill
Victoria
Peninsula and South Eastern Haematology & Oncology Group
Frankston
Victoria
Peter MacCallum Cancer
Melbourne
Victoria
St John of God Subiaco Hospital
Subiaco
Western Australia
Institut Jules-Bordet
Brussels
Belgium
Universitair Ziekenhuis Brussel
Brussels
Belgium
Universitair Ziekenhuis Antwerpen
Edegem
Belgium
AZ Sint-Lucas - Campus Sint-Lucas
Ghent
Belgium
Universitaire Ziekenhuizen Leuven
Leuven
Belgium
CHU UCL Namur site de Sainte Elisabeth
Namur
Belgium
+ 124 more sites — see the full list on the official registry below.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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