Durvalumab With or Without Olaparib as Maintenance Therapy After First-Line Treatment of Advanced and Recurrent Endometrial Cancer

Sponsor: AstraZeneca

Sponsor score: 40

ClinicalTrials ID:NCT04269200

This Phase III trial evaluates the efficacy and safety of durvalumab with platinum-based chemotherapy, followed by maintenance durvalumab with or without olaparib, in adult females with advanced or recurrent endometrial cancer. Eligible patients must have a confirmed diagnosis, be treatment-naïve, and meet specific health criteria. Interventions include durvalumab, olaparib, and standard chemotherapy.

Patient Parameters

Program Overview

A study to assess the efficacy and safety of durvalumab in combination with platinum-based chemotherapy (paclitaxel + carboplatin) followed by maintenance durvalumab with or without olaparib for patients with newly diagnosed advanced or recurrent endometrial cancer.

Description

This Phase III study will assess the efficacy and safety of durvalumab in combination with platinum-based chemotherapy (paclitaxel + carboplatin) followed by maintenance durvalumab with or without olaparib for patients with newly diagnosed advanced or recurrent endometrial cancer.

Target patient population: Adult female patients with histologically confirmed diagnosis of epithelial endometrial carcinoma (excluding sarcomas): newly diagnosed Stage III, newly diagnosed Stage IV, or recurrent endometrial cancer

Eligibility Criteria

Inclusion Criteria

  • Age ≥18 years at the time of screening and female.

  • Histologically confirmed diagnosis of epithelial endometrial carcinoma. All histologies, including carcinosarcomas, will be allowed. Sarcomas will not be allowed.

  • Patient must have endometrial cancer in one of the following categories:

    1. Newly diagnosed Stage III disease (measurable disease per RECIST 1.1 following surgery or diagnostic biopsy),
    2. Newly diagnosed Stage IV disease (with or without disease following surgery or diagnostic biopsy)
    3. Recurrence of disease (measurable or non-measurable disease per RECIST 1.1) where the potential for cure by surgery alone or in combination is poor.
  • Naïve to first line systemic anti-cancer treatment. For patients with recurrent disease only, prior systemic anti-cancer treatment is allowed only if it was administered in the adjuvant setting and there is at least 12 months from date of last dose of systemic anti-cancer treatment administered to date of subsequent relapse

  • FPPE tumor sample must be available for MMR evaluation.

  • Has Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 within 7 days of starting study treatment.

Exclusion Criteria

  • History of leptomeningeal carcinomatosis.
  • Brain metastases or spinal cord compression.
  • Prior treatment with PARP inhibitors.
  • Any prior exposure to immune-mediated therapy, including (but not limited to) other anti CTLA-4, anti-PD-1, anti-PD-L1, or anti-programmed-cell-death ligand 2 (anti-PD-L2) antibodies, excluding therapeutic anticancer vaccines.

Locations

FACILITYZIPCITYSTATE
Research Site85719TucsonArizona
Research Site94520-2278ConcordCalifornia
Research Site92093La JollaCalifornia
Research Site94158San FranciscoCalifornia
Research Site93105Santa BarbaraCalifornia
Research Site80012AuroraColorado
Research Site33316Fort LauderdaleFlorida
Research Site33612TampaFlorida
Research Site31404SavannahGeorgia
Research Site96826HonoluluHawaii

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