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
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Key Inclusion Criteria:
* Patients must be at least 18 years of age
* Pathologically documented breast cancer that:
1. Is advanced/unresectable (patients that can be treated with curative intent are not eligible) or metastatic
2. HER2-positive (IHC 3+ or IHC 2+/ISH+) based on local assessment. The local HER2 result must be from a tumour sample obtained in the metastatic setting.
3. Is documented as hormone receptor-positive (estrogen or progesterone receptor) or negative in the metastatic setting
* Patient must have adequate tumor sample from the metastatic setting for biomarker assessment
* ECOG Performance Status of 0 or 1
* Part 1
1. Disease progression on or after the last systemic therapy prior to starting study treatment
2. At least 1 prior treatment line in metastatic setting required.
* Part 2 (Modules 0 - 5)
a) No prior lines of therapy for advanced/MBC allowed
* Part 2 (Module 6 and 7) a) Zero or one prior lines of therapy for advanced/MBC allowed
CNS Inclusion
* Modules 0 - 5 Patients must have no brain metastases or stable brain metastases.
* Module 6 and 7 Patients must have untreated brain metastases not needing local therapy or previously treated brain metastases that have progressed since prior local therapy
Key Exclusion Criteria:
* Uncontrolled or significant cardiovascular disease
* Active or prior documented (non-infectious) ILD/pneumonitis that required steroids, or suspected ILD/pneumonitis that cannot be ruled out by imaging at screening
* Lung-specific intercurrent clinically significant illnesses
* Uncontrolled infection requiring IV antibiotics, antivirals, or antifungals
* Spinal cord compression or a history of leptomeningeal carcinomatosis
* Prior treatment with immune checkpoint inhibitors
* Prior treatment with an ADC containing a topoisomerase I inhibitor
* Prior treatment with tucatinib
CNS Exclusion
* Modules 0 - 5: Has untreated brain metastasis
* Module 6 and 7: Ongoing use of systemic corticosteroids for control of symptoms of brain metastases at a total daily dose of \> 2 mg dexamethasone or any brain lesion thought to require immediate local therapy
Primary outcome measure(s)
Occurrence of adverse events (AEs)- Part 1 — Up to follow-up period, approximately 53 months Occurrence of AEs in Part 1 graded according to NCI CTCAE v5.0
Occurrence of serious adverse events (SAEs)- Part 1 — Up to follow-up period, approximately 53 months Occurrence of SAEs in Part 1 graded according to NCI CTCAE v5.0
Occurrence of adverse events (AEs)- Part 2 — Up to follow-up period, approximately 53 months Occurrence of AEs in Part 2 graded according to NCI CTCAE v5.0
Occurrence of serious adverse events (SAEs)- Part 2 — Up to follow-up period, approximately 53 months Occurrence of SAEs in Part 2 graded according to NCI CTCAE v5.0
Trial sites (72)
Facility
City
Region
Status
Research Site
Fort Myers
Florida
Research Site
St. Petersburg
Florida
Research Site
Commack
New York
Research Site
Harrison
New York
Research Site
New York
New York
Research Site
New York
New York
Research Site
Columbus
Ohio
Research Site
Nashville
Tennessee
Research Site
Fort Worth
Texas
Research Site
Fairfax
Virginia
Research Site
Melbourne
Australia
Research Site
Barretos
Brazil
Research Site
Belo Horizonte
Brazil
Research Site
Natal
Brazil
Research Site
Porto Alegre
Brazil
Research Site
Porto Alegre
Brazil
Research Site
Rio de Janeiro
Brazil
Research Site
São Paulo
Brazil
Research Site
São Paulo
Brazil
Research Site
Sorocaba
Brazil
Research Site
Montreal
Quebec
Research Site
Québec
Quebec
Research Site
Toronto
Canada
Research Site
Villejuif
France
Research Site
München
Germany
Research Site
Würzburg
Germany
Research Site
Delhi
India
Research Site
Gurgaon
India
Research Site
Madurai
India
Research Site
Mumbai
India
Research Site
Bologna
Italy
Research Site
Milan
Italy
Research Site
Naples
Italy
Research Site
Rome
Italy
Research Site
Bydgoszcz
Poland
Research Site
Koszalin
Poland
Research Site
Lodz
Poland
Research Site
Lublin
Poland
Research Site
Moscow
Russia
Research Site
Moscow
Russia
+ 32 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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