Enhertu (fam-trastuzumab deruxtecan-nxki) vs Phesgo (pertuzumab, trastuzumab, and hyaluronidase)

Enhertu (fam-trastuzumab deruxtecan-nxki) vs Phesgo (pertuzumab, trastuzumab, and hyaluronidase)

Enhertu (fam-trastuzumab deruxtecan-nxki) is a targeted therapy designed for the treatment of adults with unresectable or metastatic HER2-positive breast cancer who have received two or more prior anti-HER2-based regimens in the metastatic setting. It is an antibody-drug conjugate that delivers chemotherapy directly to cancer cells by attaching to the HER2 protein. In contrast, Phesgo (pertuzumab, trastuzumab, and hyaluronidase-zzxf) is a combination of two monoclonal antibodies (pertuzumab and trastuzumab) and an enzyme (hyaluronidase) used for the treatment of HER2-positive breast cancer, which can be administered subcutaneously and is often used in the early stages of the disease as well as in the metastatic setting. The choice between these medications would depend on the specific stage and progression of the cancer, prior treatments, and the patient's overall health profile, which should be discussed with a healthcare provider.

Difference between Enhertu and Phesgo

Metric Enhertu (fam-trastuzumab deruxtecan-nxki) Phesgo (pertuzumab, trastuzumab, and hyaluronidase)
Generic name Fam-trastuzumab deruxtecan-nxki Pertuzumab, trastuzumab, and hyaluronidase-zzxf
Indications HER2-positive breast cancer HER2-positive breast cancer
Mechanism of action HER2-directed antibody and topoisomerase inhibitor Combination of HER2-directed antibodies and enzyme
Brand names Enhertu Phesgo
Administrative route IV infusion Subcutaneous injection
Side effects Nausea, fatigue, vomiting, alopecia, constipation Diarrhea, nausea, alopecia, anemia, asthenia
Contraindications History of interstitial lung disease, pneumonitis None listed
Drug class Antibody-drug conjugate Monoclonal antibodies and hyaluronidase
Manufacturer AstraZeneca/Daiichi Sankyo Genentech

Efficacy

Efficacy of Enhertu (fam-trastuzumab deruxtecan-nxki) in Breast Cancer

Enhertu (fam-trastuzumab deruxtecan-nxki) is a targeted therapy drug that has shown significant efficacy in the treatment of certain types of breast cancer. Specifically, it is approved for the treatment of adult patients with unresectable or metastatic HER2-positive breast cancer who have received two or more prior anti-HER2-based regimens in the metastatic setting. Enhertu is a conjugated monoclonal antibody that combines trastuzumab with a cytotoxic chemotherapy agent, allowing for the direct delivery of chemotherapy to cancer cells overexpressing the HER2 protein. Clinical trials have demonstrated that Enhertu significantly improves progression-free survival and overall survival in patients with HER2-positive metastatic breast cancer compared to standard treatments.

Efficacy of Phesgo (pertuzumab, trastuzumab, and hyaluronidase) in Breast Cancer

Phesgo is a combination of two monoclonal antibodies, pertuzumab and trastuzumab, with the enzyme hyaluronidase, which is used to enhance the subcutaneous delivery of the drugs. This combination is indicated for use in patients with HER2-positive early breast cancer, where it is used in the neoadjuvant (pre-surgery) setting, and for metastatic cases as well. Pertuzumab and trastuzumab target the HER2 receptor, a protein that promotes the growth of cancer cells. In clinical trials, Phesgo has been shown to be effective in reducing the size of tumors before surgery and improving survival rates in the metastatic setting when used in combination with chemotherapy.

The efficacy of Phesgo in early breast cancer was demonstrated in a pivotal clinical trial where it was compared with the intravenous formulations of trastuzumab and pertuzumab. The results showed that Phesgo was non-inferior to the intravenous formulations in terms of efficacy, with similar rates of pathologic complete response (pCR), which is a measure of the absence of invasive cancer in the breast and lymph nodes following treatment. In the metastatic setting, Phesgo, in combination with chemotherapy, has shown to improve progression-free survival, offering a convenient subcutaneous administration route that can be administered in a shorter amount of time compared to intravenous infusions.

Both Enhertu and Phesgo represent significant advancements in the treatment of HER2-positive breast cancer, offering patients new options that can improve outcomes and, in the case of Phesgo, potentially offer a more convenient administration method. It is important for healthcare providers to assess the suitability of these treatments for their patients based on individual clinical profiles and to monitor for potential side effects associated with these targeted therapies.

Regulatory Agency Approvals

Enhertu
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Phesgo
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Enhertu or Phesgo today

If Enhertu or Phesgo 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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