Perjeta (Pertuzumab) vs Margenza (margetuximab-cmkb)

Perjeta (Pertuzumab) vs Margenza (margetuximab-cmkb)

Perjeta (pertuzumab) and Margenza (margetuximab-cmkb) are both monoclonal antibodies used in the treatment of certain types of breast cancer, but they target the HER2 receptor in slightly different ways. Perjeta is often used in combination with Herceptin (trastuzumab) and chemotherapy for the treatment of HER2-positive breast cancer in both early and metastatic stages, and it works by blocking the ability of the cancer cells to receive growth signals. Margenza, on the other hand, is a newer medication that has been engineered to have an increased ability to recruit the immune system to attack cancer cells and is approved for use in patients who have previously been treated with two or more anti-HER2 regimens for metastatic disease. When deciding which medicine is right for an individual, it is crucial to consider factors such as the specific characteristics of the cancer, prior treatments, potential side effects, and the overall treatment plan as discussed with an oncologist.

Difference between Perjeta and Margenza

Metric Perjeta (Pertuzumab) Margenza (margetuximab-cmkb)
Generic name Pertuzumab Margetuximab-cmkb
Indications HER2-positive breast cancer HER2-positive breast cancer
Mechanism of action HER2/neu receptor antagonist HER2/neu receptor antagonist
Brand names Perjeta Margenza
Administrative route Intravenous infusion Intravenous infusion
Side effects Diarrhea, hair loss, neutropenia, nausea Fatigue, nausea, diarrhea, vomiting
Contraindications Hypersensitivity to pertuzumab or excipients Hypersensitivity to margetuximab-cmkb or excipients
Drug class Monoclonal antibody Monoclonal antibody
Manufacturer Genentech (Roche) MacroGenics, Inc.

Efficacy

Efficacy of Perjeta (Pertuzumab) in Breast Cancer

Perjeta (pertuzumab) is a monoclonal antibody that targets the HER2 receptor, a protein that can promote the growth of cancer cells. In the treatment of breast cancer, Perjeta is specifically indicated for use in combination with trastuzumab and chemotherapy for the treatment of patients with HER2-positive metastatic breast cancer who have not received anti-HER2 therapy or chemotherapy for metastatic disease. The efficacy of Perjeta in this setting was demonstrated in a pivotal clinical trial known as CLEOPATRA, which showed that the addition of Perjeta to trastuzumab and docetaxel chemotherapy significantly improved progression-free survival (PFS) and overall survival (OS) in patients with HER2-positive metastatic breast cancer.

Furthermore, Perjeta, in combination with trastuzumab and chemotherapy, is also approved for the neoadjuvant treatment of patients with HER2-positive, locally advanced, inflammatory, or early-stage breast cancer (either greater than 2 cm in diameter or node-positive). In this setting, Perjeta has been shown to increase the rate of pathological complete response (pCR), which is associated with a better prognosis.

Efficacy of Margenza (margetuximab-cmkb) in Breast Cancer

Margenza (margetuximab-cmkb) is another monoclonal antibody that targets the HER2 receptor on cancer cells. It is approved for use 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. The approval of Margenza was based on the results of the SOPHIA study, which demonstrated that Margenza, in combination with chemotherapy, provided a statistically significant progression-free survival benefit compared to trastuzumab plus chemotherapy in this patient population. However, an improvement in overall survival has not been established.

Both Perjeta and Margenza are part of a class of drugs known as HER2 inhibitors, which have significantly improved the outcomes for patients with HER2-positive breast cancer, a particularly aggressive form of the disease. While these drugs have different indications and have been studied in different patient populations, they both offer important options for the treatment of HER2-positive breast cancer, demonstrating efficacy in improving survival outcomes and offering additional lines of therapy for patients who have progressed on other treatments.

Regulatory Agency Approvals

Perjeta
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Margenza
  • Food and Drug Administration (FDA), USA

Access Perjeta or Margenza today

If Perjeta or Margenza are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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