Phesgo (pertuzumab, trastuzumab, and hyaluronidase) vs Tukysa (tucatinib)

Phesgo (pertuzumab, trastuzumab, and hyaluronidase) vs Tukysa (tucatinib)

Phesgo is a combination of two monoclonal antibodies, pertuzumab and trastuzumab, with hyaluronidase, used for the treatment of HER2-positive breast cancer, and is administered subcutaneously. Tukysa (tucatinib) is an oral tyrosine kinase inhibitor specifically targeting HER2, and is used in combination with other drugs for the treatment of advanced unresectable or metastatic HER2-positive breast cancer. The choice between Phesgo and Tukysa would depend on the specific characteristics of the cancer, previous treatments, and the patient's overall health status, and should be made in consultation with an oncologist.

Difference between Phesgo and Tukysa

Metric Phesgo (pertuzumab, trastuzumab, and hyaluronidase) Tukysa (tucatinib)
Generic name Pertuzumab, Trastuzumab, and Hyaluronidase-zzxf Tucatinib
Indications HER2-positive breast cancer HER2-positive breast cancer, including patients with brain metastases
Mechanism of action Monoclonal antibodies targeting HER2/neu receptor & enzyme facilitating subcutaneous administration Tyrosine kinase inhibitor targeting HER2
Brand names Phesgo Tukysa
Administrative route Subcutaneous injection Oral
Side effects Diarrhea, alopecia, nausea, fatigue, peripheral neuropathy Diarrhea, palmar-plantar erythrodysesthesia, nausea, fatigue, hepatotoxicity
Contraindications Known hypersensitivity to active substances or excipients None specifically mentioned; use caution in patients with severe hepatic impairment
Drug class Monoclonal antibodies & hyaluronidase Tyrosine kinase inhibitor
Manufacturer Genentech, Inc. Seagen Inc.

Efficacy

Efficacy of Phesgo in Breast Cancer Treatment

Phesgo, a combination of pertuzumab, trastuzumab, and hyaluronidase-zzxf, is a subcutaneous injection used in the treatment of HER2-positive breast cancer. The efficacy of Phesgo was established in the pivotal phase III FeDeriCa study, which demonstrated non-inferior levels of pertuzumab and trastuzumab in the blood (pharmacokinetics) compared to the standard intravenous (IV) administration of pertuzumab and trastuzumab. Additionally, the study showed that patients receiving Phesgo experienced a comparable rate of complete response in the breast tissue and lymph nodes as those receiving the IV formulation. This indicates that Phesgo is effective in treating HER2-positive breast cancer, offering a similar therapeutic benefit to the established IV counterparts.

Efficacy of Tukysa in Breast Cancer Treatment

Tukysa (tucatinib) is an oral tyrosine kinase inhibitor specifically designed to target HER2-positive breast cancer. The drug's efficacy was evaluated in the HER2CLIMB trial, a randomized, double-blind, placebo-controlled study. The results demonstrated a significant improvement in progression-free survival (PFS) and overall survival (OS) in patients with HER2-positive metastatic breast cancer, including those with brain metastases, when tucatinib was added to trastuzumab and capecitabine. Tukysa's ability to cross the blood-brain barrier and affect brain metastases is a notable advancement in the treatment of HER2-positive breast cancer, as central nervous system involvement is a common and challenging aspect of the disease.

Combination Therapy and Patient Outcomes

Both Phesgo and Tukysa are part of a broader treatment strategy for HER2-positive breast cancer that often involves combination therapy. Phesgo provides a more convenient administration route and has been shown to maintain efficacy and safety profiles similar to IV pertuzumab and trastuzumab. On the other hand, Tukysa's oral administration and its efficacy in treating brain metastases make it a valuable addition to the treatment regimen, especially for patients with advanced disease. The integration of these medications into treatment protocols aims to improve patient outcomes by offering effective systemic control of the disease and addressing difficult-to-treat metastases.

Conclusion

In conclusion, both Phesgo and Tukysa have demonstrated significant efficacy in the treatment of HER2-positive breast cancer. Phesgo's subcutaneous administration offers a convenient alternative to IV therapy without compromising effectiveness, while Tukysa addresses the critical need for effective treatment options for patients with brain metastases. These medications represent important advancements in the management of HER2-positive breast cancer, contributing to the potential for improved survival rates and quality of life for patients.

Regulatory Agency Approvals

Phesgo
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Tukysa
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Swissmedic (CH)

Access Phesgo or Tukysa today

If Phesgo or Tukysa 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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