DESTINY-Breast07 will investigate the safety, tolerability, and anti-tumour activity of trastuzumab deruxtecan (T-DXd) in combination with other anti-cancer agents in patients with HER2-positive Metastatic Breast Cancer
This study is modular in design allowing assessment of safety, tolerability and anti-tumour activity of T-DXd in combination with other anti-cancer agents. Combination-treatment modules will have 2 parts: a dose-finding phase (Part 1), and a dose expansion phase (Part 2); the recommended Phase 2 dose (RP2D) determined in Part 1 will be used for the dose-expansion in Part 2. The target population of interest in this study is patients with HER2-positive (as per ASCO/CAP 2018 guidelines) advanced/MBC inclusive of patients with active and stable brain metastases. Part 1 of each module will enroll patients with locally assessed HER2-positive advanced/MBC in second-line or later patients. Part 2 of each module will enroll patients with locally assessed HER2-positive breast cancer who have not received prior treatment for advanced/metastatic disease.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
245
T-DXd: administered as an IV infusion
Durvalumab: administered as an IV infusion
Paclitaxel: administered as an IV infusion
Occurrence of adverse events (AEs)- Part 1
Occurrence of AEs in Part 1 graded according to NCI CTCAE v5.0
Time frame: Up to follow-up period, approximately 53 months
Occurrence of serious adverse events (SAEs)- Part 1
Occurrence of SAEs in Part 1 graded according to NCI CTCAE v5.0
Time frame: Up to follow-up period, approximately 53 months
Occurrence of adverse events (AEs)- Part 2
Occurrence of AEs in Part 2 graded according to NCI CTCAE v5.0
Time frame: Up to follow-up period, approximately 53 months
Occurrence of serious adverse events (SAEs)- Part 2
Occurrence of SAEs in Part 2 graded according to NCI CTCAE v5.0
Time frame: Up to follow-up period, approximately 53 months
Objective Response Rate (ORR)- Part 1 and Part 2
ORR is defined as the proportion of patients who have a CR or PR, as determined by the Investigator at local site per RECIST 1.1.
Time frame: Until progression, assessed up to approximately 53 months
Progression Free Survival (PFS)- Part 1 and Part 2
PFS is defined as time from the date of randomization until the date of progression as assessed by the Investigator at local site per RECIST 1.1, or death due to any cause.
Time frame: Until progression, assessed up to approximately 53 months
Progression Free Survival 2 (PFS2)- Part 2
PFS2 is defined as time from the date of randomisation until the date of progression on next line treatment (the earliest of the progression event subsequent to first subsequent anticancer therapy) or death; second progression will be defined according to local standard clinical practice.
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Pertuzumab: administered as an IV infusion
Tucatinib administered orally (tablet) twice daily
Research Site
Fort Myers, Florida, United States
Research Site
St. Petersburg, Florida, United States
Research Site
Commack, New York, United States
Research Site
Harrison, New York, United States
Research Site
New York, New York, United States
Research Site
New York, New York, United States
Research Site
Columbus, Ohio, United States
Research Site
Nashville, Tennessee, United States
Research Site
Fort Worth, Texas, United States
Research Site
Fairfax, Virginia, United States
...and 62 more locations
Time frame: Assessed up to approximately 53 months
Duration of Response (DoR)- Part 2
DoR is defined as time from the date of first documented response until the date of documented progression or death in the absence of disease progression.
Time frame: Until progression, assessed up to approximately 53 months
Overall Survival (OS)- Part 2
OS is defined as time from the date of randomisation until the date of death due to any cause.
Time frame: Until death, assessed up to approximately 53 months
Serum Concentration of Trastuzumab Deruxtecan (T-DXd)
Determination of trastuzumab deruxtecan concentration in serum at different time points after trastuzumab deruxtecan administration
Time frame: While on study drug up to study completion, approximately 53 months
Serum Concentration of Durvalumab
Determination of durvalumab concentration in serum at different time points after administration
Time frame: While on study drug up to study completion, approximately 53 months
Serum Concentration of Pertuzumab
Determination of pertuzumab concentration in serum at different time points after administration
Time frame: While on study drug up to study completion, approximately 53 months
Plasma Concentration of Paclitaxel
Determination of paclitaxel concentration in plasma at different time points after administration
Time frame: While on study drug up to study completion, approximately 53 months
Plasma Concentration of Tucatinib
Determination of tucatinib concentration in plasma at different time points after administration
Time frame: While on study drug up to study completion, approximately 53 months
Immunogenicity of trastuzumab deruxtecan
Percentage of patients who develop ADA for trastuzumab deruxtecan
Time frame: Up to follow-up period, approximately 53 months
Immunogenicity of Durvalumab
Percentage of patients who develop ADA for durvalumab
Time frame: Up to follow-up period, approximately 53 months
Immunogenicity of Pertuzumab
Percentage of patients who develop ADA for pertuzumab
Time frame: Up to follow-up period, approximately 53 months