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Phase I/II Study of the Anti-Programmed Death Ligand-1 Durvalumab Antibody (MEDI4736) in Combination With Olaparib and/or Cediranib for Advanced Solid Tumors and Advanced or Recurrent Ovarian, Triple Negative Breast, Lung, Prostate and Colorectal Can...

Phase 1
Active, not recruiting
Conditions
Colorectal Neoplasms
Breast Neoplasms
Interventions
Registration Number
NCT02484404
Lead Sponsor
National Cancer Institute (NCI)
Brief Summary

Background:

- Durvalumab is a drug that may help people s immune systems respond to and kill cancer cells. Olaparib is a drug that may inhibit repairing DNA damage of cancer cells. Cediranib is a drug that may stop the blood vessel growth of cancer cells. This study has two components. In the phase 1 component of the study, researchers want to investigate how well participants tolerate the combination of these drugs in treating advanced solid tumors, and in the phase 2 part of this study, researchers want to study if the combination treatments are effective in ovarian cancer.

Objectives:

- Phase 2 part of the study: To determine how effective this combination is in treating ovarian cancer.

Eligibility:

- Phase 2 part of the study: Adults age 18 or older with advanced or recurrent ovarian cancer that has no standard treatment.

Design:

* Participants will be screened with medical history, physical exam, and blood and urine tests. They will have CT or MRI scans. For these, they will lie in a machine that takes pictures of their bodies.

* Phase 2 part of the study requests the participants to have tumor samples removed.

* Participants will get Durvalumab through an IV. A small plastic tube will be inserted into a vein. The drug will be given every 4 weeks until disease progression.

* Participants will take olaparib or cediranib by mouth every day.

* Every 28 days will be 1 cycle. For cycle 1, participants will have 2 study visits. All other cycles, they will have 1 visit. At these visits, they will repeat the screening procedures.

* Patients will keep a drug and diarrhea diary.

* Patients on cediranib will monitor their blood pressure and keep a blood pressure diary.

* Participants who can become pregnant, or have a partner who can become pregnant, must practice an effective form of birth control.

* After 12 cycles, participants will have 1-3 months of follow-up.

Detailed Description

Background:

Disruption of the immune checkpoint PD-1/PD-L1 pathway yielded clinical activity in subsets of advanced solid tumors, such as melanoma and lung cancer.

Olaparib (O), a PARP inhibitor (PARPi), has demonstrated single agent activity in recurrent ovarian cancer (OvCa), and subsets of prostate, triple negative breast or lung cancers.

Our recent randomized phase 2 study showed that O and cediranib (C), a VEGFR1-3 inhibitor was clinically superior to O alone in platinum-sensitive recurrent OvCa.

We hypothesize that increased DNA damage by PARP inhibition and/or reduced angiogenesis by VEGFR inhibition will complement the anti-tumor activity of an immune checkpoint inhibitor, Durvalumab, in recurrent OvCa and other solid tumors.

Objectives:

Phase I: To determine the recommended phase II dose (RP2D) and the safety of doublet therapies (Durvalumab/olaparib \[Durvalumab+O\] and Durvalumab/cediranib \[Durvalumab+C\]) and triplet therapy (Durvalumab+O+C) in patients with advanced solid tumors.

Phase II Cohort 2 non-small cell lung cancer (NSCLC); Durvalumab+O and Durvalumab+C arms: To determine clinical efficacy as measured by progression-free survival (PFS)

Phase II Cohort 3 small cell lung cancer (SCLC); Durvalumab+O arm: To determine clinical efficacy as measured by ORR

Phase II Cohort 4 metasttaic castrate-resistant prostate cancer (mCRPC); Durvalumab+O arm: To determine clinical efficacy as measured by PFS

Phase II Cohort 5 triple negative breast cancer (TNBC); Durvalumab+O arm: To determine clinical efficacy as measured by ORR

Phase II Cohort 1 OvCa; Durvalumab+O, Durvalumab+C and Durvalumab+O+C arms: To determine clinical efficacy as measured by overall response rate (ORR)

Phase II Cohort 6 colorectal cancer (CRC): C+Durvalumab arm: To determine clinical efficacy as measured by PFS

Eligibility:

Phase I: Advanced or recurrent solid tumors with evaluable disease.

Phase II Cohort 1 Durvalumab+O, Durvalumab+C and Durvalumab+O+C arms: Advanced or recurrent OvCa

Phase II Cohort 2 Durvalumab+O and Durvalumab+C arms: Advanced or recurrent NSCLC

Phase II Cohort 3 Durvalumab+O arm: Advanced or recurrent SCLC

Phase II Cohort 4 Durvalumab+O arm: mCRPC

Phase II Cohort 5 Durvalumab+O arm: Advanced or recurrent TNBC

Phase II Cohort 6 C+Durvalumab arm: Advanced or recurrent CRC

Patients must be off prior chemotherapy, radiation therapy or biologic therapy for at least 3 weeks. mCPRC patients (Cohort 4) may be on hormonal therapy with GnRH agonists/antagonists.

Adults with ECOG performance status 0-2, and adequate organ and marrow function.

Design:

Phase I: Durvalumab+O, Durvalumab+C and Durvalumab+O+C will dose escalate simultaneously. Durvalumab will be administered once every 2 weeks or once every 4 weeks until disease progression. O tablets and C will be given orally on a continuous or intermittent dosing schedule. The DLT period will be one cycle, 28 days. Patients on the 2-week schedule greater than one year will be changed to the 4-week schedule until progression.

Durvalumab+O: Durvalumab (3 mg/kg or 10 mg/kg IV every 2 weeks, or a fixed dose of 1500 mg every 4 weeks) and O tablets (150 mg or 200 mg or 300 mg BID)

Durvalumab+C: Durvalumab (3 mg/kg or 10 mg/kg IV every 2 weeks, or a fixed dose of 1500 mg every 4 weeks) and C (15 mg or 20 mg or 30 mg daily or 5 days/week)

Durvalumab+O+C: Durvalumab (a fixed dose of 1500mg every 4 weeks) with O tablets (200 mg or 300 mg BID) and C (15 mg or 20 mg 5 days/week)

Phase II Cohort 1 OvCa Durvalumab+O arm: Patients will be treated with Durvalumab+O at RP2D (O 300mg tablets bid daily and Durvalumab at 1500 mg IV every 4 weeks).

Phase II Cohort 1 OvCa Durvalumab+C arm: Patients will be treated with Durvalumab+C at RP2D (C 20mg once a day \[5 days on/2 days off\] and Durvalumab at 1500 mg every 4 weeks).

Phase II Cohort 1 OvCa Durvalumab+O+C arm: Patients with OvCa (Cohort 1) will be treated with RP2D (O tablets 300mg BID, C 20mg once a day \[5 days on/2 days off\] and Durvalumab at 1500 mg every 4 weeks).

Phase II Cohort 2 NSCLC; Durvalumab+O arm: Patients will be treated with Durvalumab+O at RP2D (O 300mg tablets bid daily and Durvalumab at 1500 mg IV every 4 weeks).

Phase II Cohort 2 NSCLC; Durvalumab+C arm: Patients will be treated with Durvalumab+C at RP2D (C 20mg once a day \[5 days on/2 days off\] and Durvalumab at 1500 mg every 4 weeks).

Phase II Cohort 3 SCLC; Durvalumab+O arm: Patients will be treated with Durvalumab+O at RP2D (O 300mg tablets bid daily and Durvalumab at 1500 mg IV every 4 weeks).

Phase II Cohort 4 mCRPC; Durvalumab+O arm: Patients will be treated with Durvalumab+O at RP2D (O 300mg tablets bid daily and Durvalumab at 1500 mg IV every 4 weeks).

Phase II Cohort 5 TNBC; Durvalumab+O arm: Patients will be treated with Durvalumab+O at RP2D (O 300mg tablets bid daily and Durvalumab at 1500 mg IV every 4 weeks).

Phase II Cohort 6 CRC; C+Durvalumab arm: Patients in the Cohort 6 will be treated with C 20mg daily alone for 14 days followed by the combination at RP2D (C 20mg once a day \[5 days on/2 days off\] and Durvalumab at 1500 mg every 4 weeks).

Phase II Correlative studies: Research samples including whole blood, CTCs, cell free DNA and plasma will be obtained at pretreatment, prior to cycle 1 day 15, prior to cycle 3 day 1 and at progression. Mandatory baseline core biopsy and two optional biopsies will be obtained.

Patients will be evaluated for toxicity every 4 weeks by CTCAEv4.0, and for response every two cycles (8 weeks) by RECIST 1.1. Patients with mCRPC (Durvalumab+O Cohort 4) will be evaluated for response initially at 8 weeks then every 12 weeks using RECIST v1.1 criteria as per the Prostate Cancer Clinical Trials Working Group 2 (PCWG2).

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
268
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
P1 Durvalumab+O+CDurvalumabPh I Durvalumab + olaparib + cediranib dose escalation
P2 Durvalumab+O+COlaparibPh II Durvalumab + olaparib + cediranib at RP2D
P2 Durvalumab+O+CCediranibPh II Durvalumab + olaparib + cediranib at RP2D
P2 Durvalumab+CCediranibPh II Durvalumab + cediranib at RP2D
P2 Durvalumab+CDurvalumabPh II Durvalumab + cediranib at RP2D
P1 Durvalumab+CDurvalumabPh I Durvalumab + cediranib dose escalation
P1 Durvalumab+OOlaparibPh I Durvalumab + olaparib dose escalation
P1 Durvalumab+ODurvalumabPh I Durvalumab + olaparib dose escalation
P1 Durvalumab+O+COlaparibPh I Durvalumab + olaparib + cediranib dose escalation
P2 Durvalumab+OOlaparibPh II Durvalumab + olaparib at RP2D
P2 Durvalumab+ODurvalumabPh II Durvalumab + olaparib at RP2D
P2 Durvalumab+O+CDurvalumabPh II Durvalumab + olaparib + cediranib at RP2D
P1 Durvalumab+CCediranibPh I Durvalumab + cediranib dose escalation
P1 Durvalumab+O+CCediranibPh I Durvalumab + olaparib + cediranib dose escalation
Primary Outcome Measures
NameTimeMethod
Ph II Determine overall response rate of Durvalumab-O and Durvalumab-C in patients with recurrent ovarian cancerevery 4 wks for toxicity and every 8 wks for response

Overall response rate

Ph I Determine the recommended phase II dose (RP2D) and the safety of doublet therapies of Durvalumab/olaparib (Durvalumab-O) and Durvalumab/cediranib (Durvalumab-C) in patients with advanced solid tumors28 days

Determination of the recommended phase II dose (RP2D) Safety: number of Adverse events

Secondary Outcome Measures
NameTimeMethod
Ph I of triplet tx:explore changes in peripheral immune subsets, plasma cytokines and circulating endothelial cells with safety and/or clinical outcome of Durvalumab+O+Cevery 28 days

Correlative laboratory research results + safety (adverse events) and/or clinical outcome

Ph II Cohort 5 TNBC; Durvalumab+O arm: To determine PFS, safety by CTCAE v4.0, and potential relationship between pretreatment tumor PD-L1 expression obtained from biopsies and clinical responseevery 28 days, every 8 weeks

ORR + safety (adverse events)

Ph II Cohort 4 mCRPC; Durvalumab+O arm: To determine ORR, safety by CTCAE v4.0, duration of response and PSA responses.every 28 days, every 8 weeks

ORR + safety (adverse events), duration of response and PSA responses.

Ph I doublet tx: explore changes in peripheral immune subsets, plasma cytokines and circulating endothelial cells with safety and/or clinical outcome of Durvalumab+Cevery 28 days

Correlative laboratory research results + safety (adverse events) and/or clinical outcome

Ph II Cohort 1 OvCa; Durvalumab+O, Durvalumab+C and Durvalumab+O+C arms: To evaluate PFS, safety by CTCAE v4.0, and potential relationship between pretreatment tumor PD-L1 expression obtained from biopsies and clinical responseevery 28 days, every 8 weeks

Progression-Free Survival (PFS) + Safety (adverse events) + PD-L1 expression obtained from biopsies and clinical response

Ph I of triplet tx::determine preliminary response rates of Durvalumab+O+C using RECIST v1.1every 8 weeks

Response: Preliminary response rate

Ph I doublet tx: determine the safety of the doublets, Durvalumab+O and Durvalumab+Cevery 28 days

Safety: number of Adverse events

Ph II Cohort 3 SCLC; Durvalumab+O arm: To determine PFS and safety by CTCAE v4.0every 28 days, every 8 weeks

PFS + Safety(adverse events)

Ph II Cohort 2 NSCLC; Durvalumab+O and Durvalumab+C arms: To determine ORR, and safety by CTCAE v4.0every 28 days, every 8 weeks

ORR + Safety (adverse events)

Ph I of triplet tx:determine the safety of Durvalumab+O+Cevery 28 days

Safety (adverse events)

Ph I of triplet tx:determine the potential relationship between PD-L1 expression obtained from archival tissue samples and clinical responseevery 28 days

PD-L1 expression obtained from archival tissue samples and clinical response

Ph I of triplet tx:determine the pharmacokinetics of the triplet and correlate with safety.Cycle 1 Days 1 and 15; Cycles 2 and beyond Day 1

Pharmacokinetics + Safety: adverse events

Ph I doublet tx:determine preliminary response rates of the doublets using RECIST v1.1every 8 wks

Response: Preliminary response rate

Ph I doublet:determine the potential relationship between PD-L1 expression obtained from archival tissue samples and clinical responseevery 28 days

PD-L1 expression obtained from archival tissue samples and clinical response

Ph I doublet tx: determine the pharmacokinetics of the doublets and correlate with safety.Cycle 1 Days 1 and 15; Cycles 2 and beyond Day 1

Pharmacokinetics + Safety: adverse events

Trial Locations

Locations (1)

National Institutes of Health Clinical Center

🇺🇸

Bethesda, Maryland, United States

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