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FDA Approves Margetuximab for Metastatic HER2-positive Breast Cancer

Evidence for efficacy was evaluated in SOPHIA study
04 Jan 2021
Anticancer agents & Biologic therapy;  Breast cancer;  Personalised medicine

On 16 December 2020, the US Food and Drug Administration (FDA) approved margetuximab-cmkb (MARGENZA, MacroGenics) in combination with chemotherapy, for the treatment of adult patients with metastatic HER2-positive breast cancer who have received two or more prior anti-HER2 regimens, at least one of which was for metastatic disease.

Efficacy was evaluated in SOPHIA (NCT02492711), a randomised, multicentre, open-label study of 536 patients with IHC 3+ or ISH-amplified HER2-positive metastatic breast cancer who had received prior treatment with other anti-HER2 therapies. Patients were randomised (1:1) to margetuximab plus chemotherapy or trastuzumab plus chemotherapy. Randomisation was stratified by chemotherapy choice (capecitabine, eribulin, gemcitabine, or vinorelbine), number of lines of therapy in the metastatic setting (≤ 2, > 2), and number of metastatic sites (≤ 2, > 2).

The main efficacy outcome measures were progression-free survival (PFS) by blinded independent central review (BICR) and overall survival (OS). Additional efficacy outcome measures were objective response rate (ORR) and duration of response (DoR) assessed by BICR.

Median PFS in the margetuximab arm was 5.8 months (95% confidence interval [CI] 5.5, 7.0) compared with 4.9 months (95% CI 4.2, 5.6) in the control arm (hazard ratio 0.76; 95% CI 0.59, 0.98; p = 0.033).

Confirmed ORR was 22% (95% CI 17, 27) with a median DoR of 6.1 months (95% CI 4.1, 9.1) in the margetuximab arm compared to an ORR of 16% (95% CI 12, 20) and median DoR of 6.0 months (95% CI 4.0, 6.9) in the control arm.

The most common adverse drug reactions (>10%) with margetuximab in combination with chemotherapy are fatigue/asthenia, nausea, diarrhoea, vomiting, constipation, headache, pyrexia, alopecia, abdominal pain, peripheral neuropathy, arthralgia/myalgia, cough, decreased appetite, dyspnoea, infusion-related reactions, palmar-plantar erythrodysesthesia, and extremity pain. The Prescribing Information includes a Boxed Warning to advise health professionals of the risks of left ventricular dysfunction and embryo-foetal toxicity.

The recommended margetuximab dose is 15 mg/kg by intravenous infusion over 120 minutes for the initial dose, then over a minimum of 30 minutes every 3 weeks for all subsequent doses. On days when both margetuximab and chemotherapy are to be administered, margetuximab may be administered immediately after chemotherapy completion. Refer to the respective Prescribing Information for each therapeutic agent administered in combination with margetuximab for the recommended dosage information, as appropriate.

Full prescribing information for MARGEZA is available here.

This review used the Assessment Aid, a voluntary submission from the applicant to facilitate the FDA’s assessment.

This application was granted fast-track designation.

Healthcare professionals should report all serious adverse events suspected to be associated with the use of any medicine and device to FDA’s MedWatch Reporting System.

For assistance with single-patient INDs for investigational oncology products, healthcare professionals may contact FDA’s Oncology Center of Excellence Project Facilitate.

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