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Clinical Trials/NCT03820141
NCT03820141
Active, not recruiting
Phase 2

Multicenter Phase II Trial of Durvalumab (MEDI4736) With Trastuzumab and Pertuzumab Combination in HER2-Enriched and HER2-Amplified Breast Cancer (DTP Trial)

The Methodist Hospital Research Institute2 sites in 1 country51 target enrollmentJune 30, 2020

Overview

Phase
Phase 2
Intervention
Durvalumab
Conditions
Breast Cancer
Sponsor
The Methodist Hospital Research Institute
Enrollment
51
Locations
2
Primary Endpoint
Pathological complete response (pCR) rate in the breast in patients with HER2-enriched and HER2-amplified breast cancer
Status
Active, not recruiting
Last Updated
12 days ago

Overview

Brief Summary

The purpose of this research study is to test the safety and effectiveness of using durvalumab with trastuzumab and pertuzumab in participants with human epidermal growth factor receptor 2 (HER2)-enriched breast cancer.

Detailed Description

The purpose of this research study is to test the safety and effectiveness of using durvalumab with trastuzumab and pertuzumab in participants with HER2-enriched breast cancer. The standard or usual pre-surgery treatment for this type of disease are drugs called trastuzumab and pertuzumab that target HER2. Studies have shown that trastuzumab and pertuzumab treatment can stimulate the body's own immune system to attack cancer cells. Durvalumab is a drug that also activates the immune system. The use of durvalumab together with trastuzumab and pertuzumab treatment may allow the immune system to work harder to kill cancer cells.

Registry
clinicaltrials.gov
Start Date
June 30, 2020
End Date
December 1, 2028
Last Updated
12 days ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Polly A. Niravath, MD

Oncologist, Houston Methodist Neal Cancer Center

The Methodist Hospital Research Institute

Eligibility Criteria

Inclusion Criteria

  • Female aged \>18 years at the time of study entry.
  • Histologically confirmed HER2-enriched (by BluePrint) and HER2-amplified (ERBB2 mRNA \>7.5-10) breast cancer.
  • Estrogen receptor and progesterone receptor negative.
  • Primary tumor greater than 1 cm diameter, measured by clinical examination and mammography or echography.
  • Any nodal status
  • Bilateral breast cancers that individually meet eligibility criteria are allowed.
  • Eastern Cooperative Oncology Group performance status of 0 or
  • Adequate organ and marrow function.
  • Baseline left ventricular ejection fraction greater than or equal to 50%, as measured by multigated acquisition scan or echocardiogram.
  • Evidence of postmenopausal status or negative serum pregnancy test for premenopausal patients. Negative serum beta-human chorionic gonadotropin pregnancy test within 7 days prior to the first dose of study treatment for premenopausal patients.

Exclusion Criteria

  • Participation in another clinical study with an investigational product within 28 days prior to the first dose of study treatment.
  • Concurrent enrollment in another clinical study, unless it is an observational (non-interventional) clinical study or during the follow-up period of an interventional study.
  • Unresolved or unstable adverse events from prior administration of another investigational drug.
  • Any concurrent chemotherapy, radiation therapy, immunotherapy, or biologic therapy for cancer treatment.
  • Major surgical procedure (as defined by the investigator) within 28 days prior to the first dose of study treatment.
  • History of allogenic organ transplantation.
  • Active or prior documented autoimmune or inflammatory disorders.
  • History of active primary immunodeficiency.
  • Active infection including tuberculosis, hepatitis B, hepatitis C, or human immunodeficiency virus.
  • Current or prior use of immunosuppressive medication within 14 days prior to the first dose of study treatment.

Arms & Interventions

Durvalumab + Trastuzumab + Pertuzumab

Durvalumab, trastuzumab, and pertuzumab will be administered on Day 1 every 3 weeks for 6 cycles. Trastuzumab will be administered as 8 mg/kg intravenous (IV) loading dose, followed by 6 mg/kg IV. Pertuzumab will be administered as 840 mg IV loading dose, followed by 420 mg. Durvalumab will be administered at a fixed dose of 1120 mg IV.

Intervention: Durvalumab

Durvalumab + Trastuzumab + Pertuzumab

Durvalumab, trastuzumab, and pertuzumab will be administered on Day 1 every 3 weeks for 6 cycles. Trastuzumab will be administered as 8 mg/kg intravenous (IV) loading dose, followed by 6 mg/kg IV. Pertuzumab will be administered as 840 mg IV loading dose, followed by 420 mg. Durvalumab will be administered at a fixed dose of 1120 mg IV.

Intervention: Trastuzumab

Durvalumab + Trastuzumab + Pertuzumab

Durvalumab, trastuzumab, and pertuzumab will be administered on Day 1 every 3 weeks for 6 cycles. Trastuzumab will be administered as 8 mg/kg intravenous (IV) loading dose, followed by 6 mg/kg IV. Pertuzumab will be administered as 840 mg IV loading dose, followed by 420 mg. Durvalumab will be administered at a fixed dose of 1120 mg IV.

Intervention: Pertuzumab

Outcomes

Primary Outcomes

Pathological complete response (pCR) rate in the breast in patients with HER2-enriched and HER2-amplified breast cancer

Time Frame: 18 weeks

Determine pCR rate in the breast in patients with HER2-enriched and HER2-amplified breast cancer

Pathological Response Rate (RCB-0 and RCB-1) Rate in the Breast in Patients With HER2-enriched and HER2-amplified Breast Cancer

Time Frame: 18 weeks

Determination of the pathologic response rate \[residual cancer burden (RCB)- 0, and RCB 1\] in the breast of durvalumab with trastuzumab and pertuzumab combination in patients with HER2-enriched and HER2-amplified breast cancer.

Secondary Outcomes

  • pCR rate in the breast in patients whose tumors have <5% and ≥5% tumor-infiltrating lymphocytes (TILs)(18 weeks)
  • pCR rate in patients with programmed cell death-ligand 1 (PD-L1)-positive and PD-L1-negative tumors(18 weeks)
  • Three-year disease-free survival (DFS) rate in patients who achieve pCR(3 years)
  • Number of participants with treatment-related adverse events(18 weeks)
  • pCR Rate in the Breast in Patients Whose Tumors Have <5% and ≥5% TILs(18 weeks)
  • pCR Rate in Patients With (PD-L1)-Positive and PD-L1-Negative Tumors(18 weeks)
  • Three-year Disease-free Survival (DFS) Rate in Patients Who Achieve pCR(3 years)
  • Number of Participants With Treatment-related Adverse Events(18 weeks)

Study Sites (2)

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