Margetuximab Plus Chemotherapy vs Trastuzumab Plus Chemotherapy in the Treatment of HER2+ Metastatic Breast Cancer

Completed · Phase 3

Conditions studied: HER-2 Positive Breast Cancer, Metastatic Neoplasm

In brief

The purpose of this study is to determine whether patients with metastatic breast cancer treated with margetuximab plus chemotherapy have longer progression free survival (PFS) and overall survival (OS) than patients treated with trastuzumab plus chemotherapy. A non-randomized sub-study cohort of approximately 88 patients will be enrolled to evaluate the safety of a reduced margetuximab infusion rate in patients receiving margetuximab either as monotherapy or in combination with chemotherapy.

Key facts

Study ID

NCT02492711

Run by

MacroGenics

People needed

624

Starts

2015-08-24

Expected to finish

2022-06-14

Last updated by the study team

2025-03-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologically-proven metastatic or locally-advanced relapsed/refractory HER2+ breast cancer based on the most recently available tumor biopsy collected from the patient. Tumors may be estrogen receptor (ER)/progesterone receptor (PgR) positive or negative.
• Have received at least 2 prior lines of anti-HER2 directed therapy in the metastatic setting, or in case of having received (neo)adjuvant pertuzumab, at least 1 prior line of anti-HER2 directed therapy in the metastatic setting. In either case, patients must have received prior treatment with pertuzumab, in the (neo)adjuvant or metastatic setting. Prior radiotherapy, hormonal therapies, and other anti-HER2 therapies are allowed.
• Prior treatment with at least one, and no more than three, lines of therapy overall in the metastatic setting. Patients must have progressed on or following, the most recent line of therapy.
• Resolution of all chemotherapy or radiation-related toxicities to ≤ Grade 1
• Life expectancy ≥ 12 weeks
• Acceptable laboratory parameters
• Women of childbearing potential must have negative pregnancy test performed within 14 days of randomization and on the first day of treatment. All subjects must agree to use an effective form of contraception for the duration of study treatment and for 7 months after the last dose of study drug.
• Infusion sub-study prior therapy requirements: Same as above, except:
• Must have received 4 or more prior lines or therapy in the metastatic setting
• Must have received prior trastuzumab, pertuzumab, and T-DM1

You may not qualify if…

• Known, untreated brain metastasis. Patients with signs or symptoms of brain metastasis must have a CT or MRI performed within 4 weeks prior to randomization to specifically exclude the presence of radiographically-detected brain metastases
• History of uncontrolled seizures within 6 months of randomization
• History of prior allogeneic bone marrow, stem-cell, or solid organ transplantation
• History of clinically significant cardiovascular disease
• Clinically-significant pulmonary compromise, including a requirement for supplemental oxygen use to maintain adequate oxygenation
• Any condition that would be a contraindication to receiving trastuzumab as described in the approved local label or a condition that would prevent treatment with the physician's choice of chemotherapy

Where it is running

• Banner MD Anderson Cancer Center — Gilbert, Arizona, United States
• Western Regional Medical Center, Inc. — Goodyear, Arizona, United States
• East Valley Hematology And Oncology — Burbank, California, United States
• UCLA Hematology Oncology Santa Monica — Los Angeles, California, United States
• UC Davis Comprehensive Cancer Center — Sacramento, California, United States
• Sharp Memorial Hospital — San Diego, California, United States
• University of California, San Francisco Helen Diller Family Comprehensive Cancer Center — San Francisco, California, United States
• Kaiser Permenente Medical Center — Vallejo, California, United States
• Poudre Valley Health Care, Inc. — Fort Collins, Colorado, United States
• MedStar Washington Hospital Center — Washington D.C., District of Columbia, United States
• Florida Cancer Specialists — Fort Myers, Florida, United States
• Memorial Cancer Institute at Memorial Regional Hospital — Hollywood, Florida, United States
• Mount Sinai Comprehensive Cancer Center — Miami Beach, Florida, United States
• Florida Cancer Specialists — New Port Richey, Florida, United States
• Orlndo Health Cancer Center — Orlando, Florida, United States
• Hem-Onc Associates — Port Saint Lucie, Florida, United States
• Palm Beach Cancer Center — West Palm Beach, Florida, United States
• Piedmont Cancer Institute, P.C. — Atlanta, Georgia, United States
• Northwest Georgia Oncology Centers, PC — Marietta, Georgia, United States
• CTCA - Southeastern Regional Medical Center — Newnan, Georgia, United States
• Kaiser Permanente Hawaii Moanalua Medical Center — Honolulu, Hawaii, United States
• Northwestern University Feinberg School of Medicine — Chicago, Illinois, United States
• Rush University Medical Center — Chicago, Illinois, United States
• Carle Cancer Center — Urbana, Illinois, United States
• Ironwood Cancer & Research Center — Chandler, Arizona, United States

Full record on ClinicalTrials.gov

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