FDA Approval Summary: Margetuximab plus Chemotherapy for Advanced or Metastatic HER2-Positive Breast Cancer.
Melanie E RoyceChristy L OsgoodAnup K AmatyaMallorie H FieroC J George ChangTiffany K RicksKrithika A ShettyJeffrey KraftJunshan QiuPengfei SongRosane CharlabJingyu YuKathryn E KingAnshu RastogiBrian JanelsinsWendy C WeinbergKathleen ClouseVicky Borders-HemphillLindsey BrownCandace Gomez-BroughtonZhong LiThuy Thanh NguyenZhihao QiuAnh-Thy LySuyoung ChangTingting GaoChi-Ming TuBellinda King-KallimanisWilliam F PierceKelly ChiangClara LeeKirsten B GoldbergJohn K LeightonShenghui TangRichard PazdurJulia A BeaverLaleh Amiri-KordestaniPublished in: Clinical cancer research : an official journal of the American Association for Cancer Research (2022)
On December 16, 2020, the FDA granted regular approval to margetuximab-cmkb (MARGENZA), in combination with chemotherapy, for the treatment of adult patients with HER2-positive (HER2+) metastatic breast cancer who have received two or more prior anti-HER2 regimens, at least one of which was for metastatic disease. Approval was based on data from SOPHIA, a multicenter, randomized, open-label, active controlled study comparing margetuximab with trastuzumab, in combination with chemotherapy. The primary efficacy endpoint was progression-free survival (PFS) by blinded independent central review. SOPHIA demonstrated a 0.9-month difference in median PFS between the two treatment arms [5.8 vs. 4.9 months, respectively; stratified HR, 0.76 (95% confidence interval: 0.59-0.98; P = 0.0334)]. Overall survival (OS) was immature at the data cut-off date of September 10, 2019. Infusion-related reactions (IRR) are an important safety signal associated with margetuximab plus chemotherapy. In SOPHIA, 13% of patients treated with margetuximab plus chemotherapy reported IRRs, of which 1.5% were grade 3. The most commonly reported adverse drug reactions (>10%) with margetuximab in combination with chemotherapy were fatigue/asthenia, nausea, diarrhea, vomiting, constipation, headache, pyrexia, alopecia, abdominal pain, peripheral neuropathy, arthralgia/myalgia, cough, decreased appetite, dyspnea, IRR, palmar-plantar erythrodysesthesia, and extremity pain. Overall, the favorable risk-benefit profile for margetuximab when added to chemotherapy supported its approval for the intended indication.
Keyphrases
- locally advanced
- chemotherapy induced
- open label
- squamous cell carcinoma
- free survival
- abdominal pain
- metastatic breast cancer
- positive breast cancer
- small cell lung cancer
- electronic health record
- low dose
- clinical trial
- rectal cancer
- emergency department
- big data
- palliative care
- spinal cord
- cross sectional
- drug administration
- neuropathic pain
- irritable bowel syndrome
- epidermal growth factor receptor
- postoperative pain