Cancer Clinical Research Unit

Inclusion Criteria: - Patients must have had surgery consisting of hysterectomy and bilateral salpingo-oophorectomy. Lymph node dissection can be performed as per institutional standards. There must be no macroscopic residual disease after surgery. - Patients must have histologically confirmed Stage I to III endometrial carcinoma which can be endometrioid, serous, clear cell, un/dedifferentiated, carcinosarcoma or mixed. - Patients' Eastern Cooperative Group (ECOG) performance status must be 0, 1, or 2. - HIV-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial. - Patients' age must be ≥ 18 years. - Patient consent must be appropriately obtained in accordance with applicable local and regulatory requirements. - Patient is able (i.e. sufficiently fluent) and willing to complete the patient-reported outcomes (PRO) questionnaires in either English, French or a validated language - Patients must be accessible for treatment and follow-up. Patients enrolled on this trial must be treated and followed at the participating centre - Protocol treatment is to begin within 10 weeks of hysterectomy/bilateral salpingo-oophorectomy Exclusion Criteria: - Prior Neoadjuvant chemotherapy for current endometrial cancer diagnosis. - Prior pelvic radiation. - Patients with a history of other malignancies, except: adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix, or other solid tumours curatively treated with no evidence of disease for ≥ 5 years. - Clinical evidence of distant metastasis as determined by pre-surgical or post-surgical imaging (CT scan of chest, abdomen and pelvis or whole-body PET-CT scan) (