Kadcyla (trastuzumab emtansine) vs Phesgo (pertuzumab, trastuzumab, and hyaluronidase)

Kadcyla (trastuzumab emtansine) vs Phesgo (pertuzumab, trastuzumab, and hyaluronidase)

Kadcyla (trastuzumab emtansine) is a targeted therapy specifically designed for the treatment of HER2-positive breast cancer, particularly in patients who have previously received trastuzumab and a taxane, separately or in combination. It combines the HER2-targeting properties of trastuzumab with the chemotherapy agent emtansine. In contrast, Phesgo (pertuzumab, trastuzumab, and hyaluronidase) is a combination of two monoclonal antibodies (pertuzumab and trastuzumab) that target the HER2 protein, along with hyaluronidase to increase the absorption, and is used for the treatment of early and metastatic HER2-positive breast cancer, often administered as a subcutaneous injection for convenience. The choice between Kadcyla and Phesgo would depend on the specific details of the patient's cancer progression, prior treatments, and the treatment setting, as well as the preference for the route of administration and the side effect profiles of the medications. It is essential for patients to discuss with their healthcare provider to determine the most appropriate treatment option based on their individual medical condition and history.

Difference between Kadcyla and Phesgo

Metric Kadcyla (trastuzumab emtansine) Phesgo (pertuzumab, trastuzumab, and hyaluronidase)
Generic name Trastuzumab emtansine Pertuzumab, trastuzumab, and hyaluronidase
Indications HER2-positive breast cancer HER2-positive breast cancer
Mechanism of action Antibody-drug conjugate targeting HER2 receptors Combination of HER2-targeted antibodies and enzyme to aid tissue penetration
Brand names Kadcyla Phesgo
Administrative route Intravenous infusion Subcutaneous injection
Side effects Fatigue, nausea, musculoskeletal pain, hemorrhage, hepatotoxicity Fatigue, alopecia, nausea, diarrhea, anemia
Contraindications Hypersensitivity to trastuzumab emtansine or excipients Hypersensitivity to active substances or excipients
Drug class Antineoplastic agent Antineoplastic combination
Manufacturer Genentech (Roche) Genentech (Roche)

Efficacy

Efficacy of Kadcyla (trastuzumab emtansine) in Breast Cancer

Kadcyla (trastuzumab emtansine) is an antibody-drug conjugate that combines the HER2 targeting properties of trastuzumab with the chemotherapy agent DM1 (emtansine). It is specifically designed for the treatment of HER2-positive metastatic breast cancer. Clinical trials have demonstrated that Kadcyla significantly improves progression-free survival (PFS) and overall survival (OS) in patients with HER2-positive metastatic breast cancer who have previously received trastuzumab and a taxane, separately or in combination. The EMILIA study, a pivotal phase III clinical trial, showed that patients treated with Kadcyla had a median PFS of 9.6 months compared to 6.4 months in those receiving lapatinib plus capecitabine, another standard treatment for this condition.

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 allows for subcutaneous administration. This combination targets the HER2 receptor, a protein overexpressed in some forms of breast cancer. Phesgo is indicated for use in patients with HER2-positive breast cancer, including those with early breast cancer (EBC), metastatic breast cancer (MBC), and those in the neoadjuvant setting. Clinical studies have shown that the efficacy of Phesgo is comparable to that of intravenous administrations of pertuzumab and trastuzumab. The pivotal study, the FEATHER trial, demonstrated non-inferior levels of pertuzumab and trastuzumab in the blood, indicating similar efficacy in the treatment of HER2-positive breast cancer.

Both Kadcyla and Phesgo have been evaluated in a number of clinical settings and have shown efficacy in improving outcomes for patients with HER2-positive breast cancer. While Kadcyla is primarily used in the metastatic setting after prior treatments, Phesgo offers a more convenient administration route and is used across different stages of breast cancer. The use of these targeted therapies has been a significant advancement in the treatment of HER2-positive breast cancer, a particularly aggressive form of the disease.

It is important to note that the efficacy of these medications can vary based on individual patient factors and the specifics of their disease. As with any medical treatment, the use of Kadcyla and Phesgo should be guided by a healthcare professional, taking into account the patient's overall health, disease characteristics, and prior treatments. Ongoing research continues to refine the use of these medications and to explore their efficacy in combination with other treatments for breast cancer.

Regulatory Agency Approvals

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

Access Kadcyla or Phesgo today

If Kadcyla 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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