Perjeta (Pertuzumab) vs Tukysa (tucatinib)

Perjeta (Pertuzumab) vs Tukysa (tucatinib)

Perjeta (pertuzumab) is a monoclonal antibody designed to target the HER2 receptor, a protein overexpressed in some breast cancers, and is often used in combination with other drugs like trastuzumab and chemotherapy. Tukysa (tucatinib) is a small molecule tyrosine kinase inhibitor that also targets HER2-positive breast cancer, but it is typically used in combination with trastuzumab and capecitabine for patients with advanced unresectable or metastatic HER2-positive breast cancer, including those with brain metastases. The choice between Perjeta and Tukysa would depend on the specific characteristics of the cancer, previous treatments, the presence of brain metastases, and the patient's overall health status, which should be discussed with an oncologist to determine the most appropriate treatment plan.

Difference between Perjeta and Tukysa

Metric Perjeta (Pertuzumab) Tukysa (tucatinib)
Generic name Pertuzumab Tucatinib
Indications HER2-positive breast cancer HER2-positive breast cancer, including those with brain metastases
Mechanism of action HER2/neu receptor antagonist Tyrosine kinase inhibitor
Brand names Perjeta Tukysa
Administrative route IV infusion Oral
Side effects Diarrhea, rash, nausea, fatigue, mucosal inflammation, etc. Diarrhea, palmar-plantar erythrodysesthesia, nausea, fatigue, hepatotoxicity, etc.
Contraindications Hypersensitivity to pertuzumab or excipients Hypersensitivity to tucatinib or excipients
Drug class Monoclonal antibody Tyrosine kinase inhibitor
Manufacturer Genentech (Roche) Seagen Inc.

Efficacy

Efficacy of Perjeta (Pertuzumab) in Breast Cancer

Perjeta (pertuzumab) is a monoclonal antibody designed to target the HER2 receptor, a protein that is overexpressed in some types of breast cancer. Pertuzumab works by binding to the HER2 receptor and inhibiting the receptor's ability to receive growth signals, thus impeding the growth and spread of cancer cells. When used in combination with trastuzumab and chemotherapy, pertuzumab has been shown to significantly improve progression-free survival in patients with HER2-positive metastatic breast cancer. This combination has also demonstrated an increase in overall survival in this patient population, making it a valuable treatment option for HER2-positive breast cancer.

In the neoadjuvant setting, which involves treatment before surgery, pertuzumab in combination with trastuzumab and chemotherapy has been shown to increase the rate of pathologic complete response. This means that following treatment, no invasive cancer can be detected in the breast or lymph nodes during surgery. This response is associated with a better prognosis and a lower risk of recurrence, highlighting the efficacy of pertuzumab in early-stage breast cancer treatment.

Efficacy of Tukysa (tucatinib) in Breast Cancer

Tukysa (tucatinib) is an oral tyrosine kinase inhibitor that specifically targets HER2-positive breast cancer. Tucatinib works by selectively inhibiting the activity of the HER2 kinase, leading to the inhibition of the downstream signaling pathways that promote the growth of cancer cells. In a pivotal clinical trial, tucatinib combined with trastuzumab and capecitabine showed a significant improvement in progression-free survival and overall survival in patients with HER2-positive metastatic breast cancer, including those with brain metastases. This finding is particularly noteworthy as brain metastases are a common and challenging complication in HER2-positive breast cancer, and tucatinib is one of the few treatments that have demonstrated efficacy in this population.

Moreover, the addition of tucatinib to the standard therapy has been associated with a higher objective response rate, meaning more patients experienced a significant reduction in tumor size. The benefit of tucatinib has been observed across various subgroups of patients, including those with prior treatments and varying degrees of tumor burden. This underscores the potential of tucatinib as a targeted treatment that can be tailored to individual patient needs in the management of advanced HER2-positive breast cancer.

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

Access Perjeta or Tukysa today

If Perjeta 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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