Endometrial cancer
Conditions
Interventions
Experimental: Arm A: T-DXd
Participants will receive T-DXd 5.4 mg/kg intravenously (IV) once every 3 weeks (Q3W) with or without radiotherapy
Active Comparator: Arm B: Standard of Care Chemotherapy
P
Sponsors
Inoguchi Akihiro
AstraZeneca
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: - Adults >=18 years at the time the ICF is signed (Please follow local regulatory requirements if the legal age of consent for trial participation is >18 years old). - Has histologically confirmed diagnosis of epithelial endometrial carcinoma. All histology's are allowed except for sarcomas (carcinosarcomas are allowed). - Is newly diagnosed FIGO 2023 Stage IIC (including Stage IICmp53abn) or Stage III. Note: FIGO 2023 Stage IIC includes disease with aggressive histological types with any myometrial involvement. FIGO 2023 Stage III includes disease with local and/or regional spread of the tumor of any histological subtype. - Has HER2-expression (IHC 3+/2+) per 2016 ASCO-CAP gastric cancer IHC scoring guidelines as confirmed by central laboratory testing. - Has adequate archived tumor tissue sample (sample from surgery is strongly recommended) available for assessment of HER2 status by central laboratory.
Exclusion criteria
Exclusion criteria: - Has uterine mesenchymal tumor such as an endometrial stromal sarcoma, leiomyosarcoma, or other types of pure sarcomas. Adenosarcomas are also not allowed. - Has recurrent or FIGO 2023 Stage IV. - Has measurable residual tumor after surgery as determined by BICR assessment. - Is known to have a POLE mutation from an approved and/or validated local test, according to local regulations, if available - Has a medical history of MI within 6 months before randomization/enrollment, symptomatic CHF (NYHA Class II to IV). Participants with troponin levels above ULN at SCR (as defined by the manufacturer), and without any MI related symptoms should have a cardiologic consultation during SCR period to rule out MI. - Has a QTcF prolongation to > 480 msec based on average of the SCR triplicate12-lead ECG. - Clinically severe pulmonary compromise resulting from intercurrent pulmonary illnesses including, but not limited to, any underlying pulmonary disorder (ie, pulmonary emboli within 3 months of the trial enrollment, severe asthma, severe COPD, restrictive lung disease, pleural effusion, etc.) and any autoimmune, connective tissue, or inflammatory disorder with potential pulmonary involvement (eg, rheumatoid arthritis, Sjogren's syndrome, sarcoidosis, etc.), or prior pneumonectomy. - Has a history of (noninfectious) ILD/pneumonitis that required corticosteroids, has current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at SCR.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Disease-Free Survival [Time Frame: From randomization to the first documented local regional recurrence, distant metastasis, or death due to any cause, whichever occurs first, up to approximately 51 months] Disease-Free Survival will be assessed radiographically by BICR or by histopathologic confirmation of disease recurrence per local assessment. | — |
Secondary
| Measure | Time frame |
|---|---|
| Overall Survival [Time Frame: From randomization to the date of death due to any cause, up to approximately 63 months] Overall Survival is defined as the time interval from the date of randomization to the date of death due to any cause. | — |
Countries
Argentina, Brazil, Canada, Chile, China, France, Germany, Greece, India, Israel, Italy, Japan, Korea, Poland, Portugal, Spain, Taiwan, Thailand, Unite States
Contacts
Public ContactContact for Clinical Trial Information
Daiichi Sankyo Co., Ltd.
Outcome results
None listed