A Phase III Study of Dato-DXd With or Without Durvalumab Compared With Investigator's Choice of Chemotherapy in Combination With Pembrolizumab in Patients With PD-L1 Positive Locally Recurrent Inoperable or Metastatic Triple-negative Breast Cancer (TROPION-Breast05)
Dato-DXd: Provided in 100mg vials. IV infusion. Experimental drug.
Durvalumab: Provided in 500mg vials. IV infusion. Experimental drug.
Paclitaxel: IV infusion. Active comparator.
Nab-paclitaxel: IV infusion. Active comparator.
Gemcitabine: IV infusion. Active comparator.
Carboplatin: IV infusion. Active comparator.
Pembrolizumab: IV infusion. Active comparator.
Study summary
This is a Phase III, randomised, open-label, 3-arm, multicentre, international study assessing the efficacy and safety of Dato-DXd with or without durvalumab compared with investigator's choice chemotherapy in combination with pembrolizumab in participants with PD-L1 positive locally recurrent inoperable or metastatic TNBC.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Key Inclusion Criteria
* Histologically or cytologically documented locally recurrent inoperable, which cannot be treated with curative intent, or metastatic TNBC, as defined by the ASCO-CAP guidelines.
* ECOG PS 0 or 1.
* Participants are expected to provide an FFPE tumour sample collected from a locally recurrent inoperable or metastatic tumour. Alternatively, an archival FFPE tumour sample can be submitted; it must have been collected ≤ 3 years prior to the participant signing informed consent (screening start).
* PD-L1 positive TNBC based on results from an appropriately validated investigational PD-L1 (22C3) assay (CPS ≥ 10) from a sponsor designated central laboratory.
* No prior chemotherapy or other systemic anti-cancer therapy for metastatic or locally recurrent inoperable breast cancer.
\- Patients with recurrent disease will be eligible if they have completed treatment for Stage I-III breast cancer, if indicated, and ≥6 months have elapsed between completion of treatment with curative intent and the first documented recurrence.
* Eligible for one of the chemotherapy options listed as ICC (paclitaxel, nab-paclitaxel, or gemcitabine + carboplatin).
* Measurable disease as per RECIST 1.1.
* Adequate bone marrow reserve and organ function.
* Male and female participants of childbearing potential must agree to use protocol-specified method(s) of contraception.
Key Exclusion Criteria
* As judged by investigator, any evidence of diseases (such as severe or uncontrolled medical conditions including systemic diseases, uncontrolled hypertension, serious gastrointestinal conditions associated with diarrhoea, chronic diverticulitis or previous complicated diverticulitis, history of allogeneic organ transplant, and active bleeding diseases, ongoing and active infection, significant cardiac conditions, substance abuse, psychiatric illness/social situation or psychological conditions) which, in the investigator's opinion, makes it undesirable for the participant to participate in the study or that would jeopardize compliance with the protocol.
* History of another primary malignancy except for malignancy treated with curative intent with no known active disease within 2 years before Cycle 1 Day 1 and of low potential risk for recurrence.
* Participants with a history of previously treated neoplastic spinal cord compression or treated, clinically inactive brain metastases that are no longer symptomatic, who require no treatment with corticosteroids or anticonvulsants, may be included in the study if they have recovered from acute toxic effects of radiotherapy.
\- Participants with treated clinically inactive brain metastases that are no longer symptomatic, who require no treatment with corticosteroids or anticonvulsants, may be included in the study if they have recovered from acute toxic effects of radiotherapy.
* Uncontrolled infection requiring IV antibiotics, antivirals or antifungals.
* Active or uncontrolled hepatitis B or C virus infection.
* Known HIV infection that is not well controlled.
* Uncontrolled or significant cardiac disease.
* History of non-infectious ILD/pneumonitis (including radiation pneumonitis) that required steroids, current ILD/pneumonitis, or suspected ILD/pneumonitis that cannot be ruled out by imaging at screening.
* Clinically severe pulmonary function compromise.
* Clinically significant corneal disease.
* Active or prior documented autoimmune or inflammatory disorders.
* Prior exposure to any treatment including ADC containing a chemotherapeutic agent targeting topoisomerase I and TROP2-targeted therapy.
* Any concurrent anti-cancer treatment.
* Participants with a known severe hypersensitivity to PD-1/PD-L1 inhibitors or Dato-DXd.
* Currently pregnant (confirmed with positive pregnancy test), breastfeeding or planning to become pregnant.
Primary outcome measure(s)
Progression Free Survival (PFS) — From randomisation until progression per RECIST 1.1 as assessed by BICR, or death due to any cause (anticipated to be up to 33 months). PFS is defined as time from randomisation until progression per RECIST 1.1 as assessed by BICR, or death due to any cause. The comparison will include all randomised participants, as randomised, regardless of whether the participant withdraws from randomised therapy, receives another anticancer therapy or clinically progresses prior to RECIST 1.1 progression.
However, if the participant progresses or dies immediately after 2 or more consecutive missed visits, the participant will be censored at the time of the latest evaluable assessment prior to the 2 missed visits.
The measure of interest is the HR of PFS.
Trial sites (320)
Facility
City
Region
Status
Research Site
Daphne
Alabama
Recruiting
Research Site
Springdale
Arkansas
Recruiting
Research Site
Duarte
California
Withdrawn
Research Site
Fountain Valley
California
Not Yet Recruiting
Research Site
Glendale
California
Recruiting
Research Site
Sacramento
California
Recruiting
Research Site
Santa Rosa
California
Withdrawn
Research Site
Aurora
Colorado
Recruiting
Research Site
Denver
Colorado
Not Yet Recruiting
Research Site
New Haven
Connecticut
Recruiting
Research Site
Altamonte Springs
Florida
Not Yet Recruiting
Research Site
Jacksonville
Florida
Withdrawn
Research Site
Miami
Florida
Recruiting
Research Site
Palm Bay
Florida
Withdrawn
Research Site
Plantation
Florida
Recruiting
Research Site
Atlanta
Georgia
Suspended
Research Site
Honolulu
Hawaii
Withdrawn
Research Site
Chicago
Illinois
Recruiting
Research Site
Decatur
Illinois
Withdrawn
Research Site
Elmhurst
Illinois
Withdrawn
Research Site
Naperville
Illinois
Withdrawn
Research Site
New Albany
Indiana
Withdrawn
Research Site
Des Moines
Iowa
Recruiting
Research Site
Lexington
Kentucky
Withdrawn
Research Site
Louisville
Kentucky
Withdrawn
Research Site
Louisville
Kentucky
Withdrawn
Research Site
Baton Rouge
Louisiana
Withdrawn
Research Site
Baton Rouge
Louisiana
Recruiting
Research Site
Baltimore
Maryland
Withdrawn
Research Site
Columbia
Maryland
Recruiting
Research Site
Boston
Massachusetts
Withdrawn
Research Site
Worcester
Massachusetts
Withdrawn
Research Site
Detroit
Michigan
Recruiting
Research Site
Grand Rapids
Michigan
Withdrawn
Research Site
Saint Paul
Minnesota
Recruiting
Research Site
Hattiesburg
Mississippi
Withdrawn
Research Site
St Louis
Missouri
Recruiting
Research Site
Albuquerque
New Mexico
Recruiting
Research Site
Albany
New York
Withdrawn
Research Site
New York
New York
Recruiting
+ 280 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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