Perjeta (Pertuzumab) vs Trodelvy (sacituzumab govitecan-hziy)

Perjeta (Pertuzumab) vs Trodelvy (sacituzumab govitecan-hziy)

Perjeta (pertuzumab) is a monoclonal antibody designed to target the HER2 receptor, which is overexpressed in some types of breast cancer, and it is often used in combination with other therapies for the treatment of HER2-positive breast cancer. Trodelvy (sacituzumab govitecan-hziy), on the other hand, is an antibody-drug conjugate that targets the Trop-2 receptor and is used to treat triple-negative breast cancer, which lacks the three most common types of receptors known to fuel most breast cancer growth—estrogen, progesterone, and the HER-2 gene. The choice between Perjeta and Trodelvy would largely depend on the specific characteristics of the breast cancer being treated, including receptor status and previous treatments, and should be made in consultation with an oncologist.

Difference between Perjeta and Trodelvy

Metric Perjeta (Pertuzumab) Trodelvy (sacituzumab govitecan-hziy)
Generic name Pertuzumab Sacituzumab govitecan-hziy
Indications HER2-positive breast cancer Metastatic triple-negative breast cancer, Urothelial cancer
Mechanism of action HER2/neu receptor antagonist Antibody-drug conjugate targeting Trop-2
Brand names Perjeta Trodelvy
Administrative route Intravenous Intravenous
Side effects Diarrhea, rash, nausea, fatigue, mucosal inflammation, etc. Neutropenia, diarrhea, nausea, fatigue, anemia, etc.
Contraindications Hypersensitivity to pertuzumab or its excipients Hypersensitivity to sacituzumab govitecan-hziy or its excipients
Drug class Monoclonal antibody Antibody-drug conjugate
Manufacturer Genentech (Roche) Gilead Sciences

Efficacy

Efficacy of Perjeta (Pertuzumab) in Breast Cancer

Perjeta (pertuzumab) is a monoclonal antibody that targets the HER2 receptor, a protein overexpressed in some types of breast cancer. Pertuzumab is designed to prevent the HER2 receptor from pairing with other HER receptors on the surface of cancer cells, which can inhibit tumor growth. It is often used in combination with trastuzumab and chemotherapy. Clinical trials have demonstrated that the addition of pertuzumab to standard therapy can significantly improve progression-free survival and overall survival in patients with HER2-positive metastatic breast cancer. The CLEOPATRA study, a pivotal phase III trial, showed that patients receiving pertuzumab in combination with trastuzumab and docetaxel had a median progression-free survival that was 6.1 months longer than those receiving the standard therapy alone.

Efficacy of Trodelvy (Sacituzumab Govitecan-hziy) in Breast Cancer

Trodelvy (sacituzumab govitecan-hziy) is an antibody-drug conjugate that targets the Trop-2 antigen, which is expressed in the majority of breast cancers. The drug links an anti-Trop-2 antibody with a chemotherapy agent, allowing for direct delivery of the chemotherapeutic to the cancer cells. This targeted approach helps to minimize the impact on healthy cells. Trodelvy has shown a significant impact on patients with metastatic triple-negative breast cancer (TNBC), a particularly aggressive and difficult-to-treat form of the disease. In a phase III trial (ASCENT), sacituzumab govitecan-hziy demonstrated a median progression-free survival of 5.6 months compared to 1.7 months with chemotherapy, and an overall survival of 12.1 months compared to 6.7 months, respectively.

Comparative Efficacy in Different Subtypes of Breast Cancer

It's important to note that the efficacy of Perjeta and Trodelvy varies significantly based on the breast cancer subtype. Perjeta is specifically indicated for HER2-positive breast cancer, a subtype where HER2 protein overexpression is a driving factor in cancer progression. On the other hand, Trodelvy is used in the treatment of triple-negative breast cancer, which lacks the expression of estrogen receptors, progesterone receptors, and HER2, and therefore does not respond to hormonal therapy or therapies targeting HER2. The targeted mechanisms of action of these drugs underpin their efficacy in these distinct patient populations.

Conclusion

In conclusion, both Perjeta and Trodelvy have shown to be effective in their respective indications for breast cancer treatment. Perjeta, in combination with other therapies, has improved outcomes for patients with HER2-positive breast cancer, while Trodelvy has emerged as a significant advancement for patients with metastatic triple-negative breast cancer. The use of these targeted therapies represents a shift towards personalized medicine in oncology, where treatment is increasingly tailored to the specific characteristics of a patient's 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)
Trodelvy
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Perjeta or Trodelvy today

If Perjeta or Trodelvy 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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