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Purpose

This is a Phase IB/II multi-cohort study designed to evaluate the efficacy and safety of targeted agents with or without cancer immune checkpoint therapy with atezolizumab in participant with recurrent and/or persistent endometrial cancer. The main protocol provides a platform for genomic screening with homogeneous basic eligibility criteria in order to direct study participants into biomarker-matched study cohorts consisting of testing targeted agents.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Recurrent or persistent endometrial carcinoma which has progressed or recurred after at least 1, but no more than 2, prior lines of therapy. Prior hormonal therapies (e.g., tamoxifen, aromatase inhibitors) will not count toward the prior regimen limit. Chemotherapy given in conjunction with radiotherapy as a radiosensitizer will be counted as a systemic therapeutic regimen. - Measurable disease per RECIST 1.1 - Availability of a representative tumor specimen that is suitable for determination of biomarker status via central testing (F1CDx) OR If a patient has a prior F1CDx report from 1 September 2019 or later, those NGS results can be used to determine biomarker status as long as the tumor tissue used in the report was obtained within 5 years prior to prescreening and appropriate signed consent is obtained from the patient. - Life expectancy > 12 weeks - Recovery from effects of recent radiotherapy, surgery, or chemotherapy

Exclusion Criteria

  • Endometrial tumors with the following histologies: squamous carcinomas, sarcomas - Other invasive malignancies within the last 5 years, except for non-melanoma skin cancer with no evidence of disease within the past 5 years AND localized breast cancer with previous adjuvant chemotherapy treatment for breast cancer completed > 5 years ago - Synchronous primary invasive ovarian or cervical cancer - Have an active or history of autoimmune disease or immune deficiency - Have a history of idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced pneumonitis, idiopathic pneumonitis, or evidence of active pneumonitis based on a screening chest computed tomography (CT) scan - Active tuberculosis - Severe infections within 4 weeks - Have received therapeutic oral or IV antibiotic medication within 2 weeks, except prophylactic antibiotic medication - Have significant cardiovascular disease - Are administered treatment with a live attenuated vaccine within 4 weeks, or anticipation of need for such a vaccine during the course of the study - Have prior allogeneic bone marrow transplantation or solid organ transplant - History of treatment with systemic immunostimulatory agents (including but not limited to interferons, interleukin-2) within 4 weeks or 5 half-lives of the drug, whichever is longer, prior to initiation of study treatment - History of treatment with systemic immunosuppressive medications within 2 weeks except acute, low-dose, systemic immunosuppressant medications, corticosteroids for chronic obstructive pulmonary disease and asthma, or mineralocorticoids and low-dose corticosteroids for participants with orthostatic hypotension or adrenocortical insufficiency - Have a history or clinical evidence of any untreated CNS disease, seizures not controlled with standard medical therapy, or history of cerebrovascular accident (stroke), transient ischemic attack or subarachnoid hemorrhage within 6 months AFT-50A Specific Exclusion Criteria: ● Prior treatment with T-cell costimulating or immune checkpoint blockade therapies including, but not limited to, CD137 agonists, anti-PD-1, anti-PD-L1, and anti-CTLA-4 therapeutic antibodies Note: Additional study cohort specific inclusion and exclusion criteria may apply based on cohort assignment.

Study Design

Phase
Phase 1/Phase 2
Study Type
Interventional
Allocation
Non-Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Atezolizumab and Bevacizumab Cohort 		Following the submission of tumor tissue for the FoundationOne® companion diagnostic (F1CDx) test, participants with no specified gene signatures will be enrolled in this cohort. Twenty participants will be enrolled. Once twenty participants are enrolled, the cohort will be closed to further enrollment. Participants in this study cohort will commence treatment as specified on Day 1 of each cycle.
  • Drug: Atezolizumab - 28 Day Cycle
    Atezolizumab will be given to participants intravenously at a dosage of 1680 mg on day 1 of each 28-day cycle.
    Other names:
    • Tecentriq
    • L01XC32
  • Drug: Bevacizumab
    Bevacizumab will be given to participants intravenously at a dosage of 10mg per participant kilogram every 2 weeks of the 28-day cycle.
    Other names:
    • Avastin
    • L01XC07
Experimental
Atezolizumab and Ipatasertib Cohort 		Following the submission of tumor tissue for the FoundationOne® companion diagnostic (F1CDx) test, participants with PIK3CA/AKT1/PTEN-altered tumors will be enrolled in this cohort. Twenty participants will be enrolled. Once twenty participants are enrolled, the cohort will be closed to further enrollment. Participants in this study cohort will commence treatment as specified on Day 1 of each cycle.
  • Drug: Atezolizumab - 28 Day Cycle
    Atezolizumab will be given to participants intravenously at a dosage of 1680 mg on day 1 of each 28-day cycle.
    Other names:
    • Tecentriq
    • L01XC32
  • Drug: Ipatasertib
    Ipatasertib will be given as an orally at a dosage of 400 mg once daily for 21 days of each 28-day cycle.
    Other names:
    • RG7440
    • GDC-0068
Experimental
Atezolizumab and Talazoparib Cohort 		Following the submission of tumor tissue for the FoundationOne® companion diagnostic (F1CDx) test, participants with tumors that have a ≥16%genomic loss of heterozygosity (LOH) will be assigned to this cohort. Twenty participants will be enrolled. Once twenty participants are enrolled, the cohort will be closed to further enrollment. Participants in this study cohort will commence treatment as specified on Day 1 of each cycle.
  • Drug: Atezolizumab - 28 Day Cycle
    Atezolizumab will be given to participants intravenously at a dosage of 1680 mg on day 1 of each 28-day cycle.
    Other names:
    • Tecentriq
    • L01XC32
  • Drug: Talazoparib
    Talazoparib will be given in an orally at a dosage of 1 mg once daily for each day of the 28-day cycle.
    Other names:
    • Talzenna
    • L01XX60
Experimental
Atezolizumab and Trastuzumab emtansine (TDM-1) Cohort 		Following the submission of tumor tissue for the FoundationOne® companion diagnostic (F1CDx) test, participants with tumors that with an amplification of ERBB2/HER2 will be assigned to this cohort. Twenty participants will be enrolled. Once twenty participants are enrolled, the cohort will be closed to further enrollment. Participants in this study cohort will commence treatment as specified on Day 1 of each cycle.
  • Drug: Trastuzumab emtansine
    Trastuzumab emtansine be given to participants intravenously at a dosage of 3.6 mg per participant kilogram, on day 1 of each 21-day cycle.
    Other names:
    • T-DM1
    • Kadcyla
  • Drug: Atezolizumab - 21 Day Cycle
    Atezolizumab will be given to participants intravenously at a dosage of 1200 mg on day 1 of each 21-day cycle.
    Other names:
    • Tecentriq
    • L01XC32
Experimental
Atezolizumab and Tiragolumab Cohort 		Following the submission of tumor tissue for the FoundationOne® companion diagnostic (F1CDx) test, participants with tumor type MSI-H and/or tTMB >=10 mut/mb will be assigned to this cohort. Twenty participants will be enrolled initially. Once twenty participants are enrolled, the cohort may be expanded if a positive signal is shown. Participants in this study cohort will commence treatment as specified on Day 1 of each cycle.
  • Drug: Atezolizumab - 28 Day Cycle
    Atezolizumab will be given to participants intravenously at a dosage of 1680 mg on day 1 of each 28-day cycle.
    Other names:
    • Tecentriq
    • L01XC32
  • Drug: Tiragolumab
    Tiragolumab will be given to participants intravenously at a dosage of 840 mg on day 1 of each 28-day cycle.
Experimental
Inavolisib and Letrozole Cohort 		Following the submission of tumor tissue for the FoundationOne® companion diagnostic (F1CDx) test, participants with tumors that with PIK3CA activating mutations in the absence of PTEN loss-of-function alterations or AKT1 activating mutations will be assigned to this cohort. Twenty-four participants will be enrolled. Once twenty-four participants are enrolled, the cohort will be closed to further enrollment. Participants in this study cohort will commence treatment as specified on Day 1 of each cycle.
  • Drug: Inavolisib
    Inavolisib will be given in an orally at a dosage of 9 mg once daily for each day of the 28-day cycle.
    Other names:
    • GDC-0077
  • Drug: Letrozole
    Letrozole will be given orally at a dosage of 2.5 mg once daily for each day of the 28-day cycle.
    Other names:
    • Femara
Experimental
Giredestrant and Abemaciclib 		Following the submission of tumor tissue for the FoundationOne® companion diagnostic (F1CDx) test, participants with tumors that are RB1 intact with a local grade 1-2 estrogne receptor positive (ER+) are assigned to this cohort. Twenty-four participants will be enrolled. Once twenty-four participants are enrolled, the cohort will be closed to further enrollment. Participants in this study cohort will commence treatment as specified on Day 1 of each cycle.
  • Drug: Giredestrant
    Giredestrant will be given orally at a dosage of 30 mg once daily for each day of the 28-day cycle.
    Other names:
    • GDC-9545
  • Drug: Abemaciclib
    Giredestrant will be given orally at a dosage of 150 mg twice daily for each day of the 28-day cycle.
    Other names:
    • Verzenio

Recruiting Locations

University of Kansas Cancer Center
Westwood, Kansas 66205
Contact:
Andrea Jewell, MD

More Details

Status
Recruiting
Sponsor
Alliance Foundation Trials, LLC.

Study Contact

Quality Management and Compliance
617-732-8727
ClinicalTrials.Queries@alliancefoundationtrials.org

Detailed Description

This is a Phase IB/II multi-cohort study designed to evaluate the efficacy and safety of targeted agents with or without cancer immune checkpoint therapy with atezolizumab in participants with recurrent and/or persistent endometrial cancer. This biomarker-driven study provides a platform whereby participants with persistent/recurrent endometrial cancer will be placed into study cohorts evaluating targeted agents selected on the basis of the tumor's specific genomic profile. Prospective participants with persistent and/or recurrent endometrial cancer will be prescreened within 60 days of treatment assignment to have a tumor tissue sample submitted for next-generation sequencing (NGS) using FoundationOne® companion diagnostic (CDx) testing prior to entering screening. If a participant has FoundationOne® CDx testing within five years of enrollment, the previous tumor tissue may be re-analyzed for use in the study. Depending on the cohort assignment per the tumor's biomarker profile, participants will be assigned to the AFT-50A Protocol (atezolizumab+targeted agent) or the AFT-50B Protocol (non-atezolizumab targeted agents). The current study cohorts are as follows: AFT-50A Cohorts - Atezolizumab + Bevacizumab doublet - Closed to Accrual - Atezolizumab + Ipatasertib doublet - Closed to Accrual - Atezolizumab + Talazoparib doublet - Atezolizumab + Trastuzumab emtansine (TDM-1) doublet - Closed to Accrual - Atezolizumab + Tiragolumab doublet AFT-50B Cohorts - Inavolisib + Letrozole doublet - Giredestrant + Abemaciclib doublet It is anticipated that approximately 20 participants will be enrolled in each study cohort in AFT-50A and 24 participants in each study cohort in AFT-50B, unless otherwise specified for a given cohort due to statistical considerations. Each study cohort will open/close independently of other study cohorts. Once a study cohort reaches the prespecified number of participants, it will be closed to further enrollment, unless an expansion phase is planned. The study is structured to allow for additional cohorts to be added as the study progresses. These additional study cohorts may be proposed by investigators, but requires approval by the Steering Committee in order to be added to the protocol.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.