Tecentriq (Atezolizumab) vs Perjeta (Pertuzumab)

Tecentriq (Atezolizumab) vs Perjeta (Pertuzumab)

Tecentriq (Atezolizumab) is an immune checkpoint inhibitor specifically targeting the PD-L1 protein, which is used primarily for the treatment of certain types of bladder, lung, and triple-negative breast cancers by enhancing the body's immune response against cancer cells. Perjeta (Pertuzumab), on the other hand, is a monoclonal antibody that targets the HER2 receptor, and it is used in combination with other medications to treat HER2-positive breast cancer, which is a breast cancer that tests positive for a protein called human epidermal growth factor receptor 2, which promotes the growth of cancer cells. When deciding which medicine is right for an individual, it is crucial to consider the specific type of cancer, its molecular characteristics, and the overall treatment plan as determined by a healthcare professional, since each medication is designed to target different mechanisms of cancer growth and progression.

Difference between Tecentriq and Perjeta

Metric Tecentriq (Atezolizumab) Perjeta (Pertuzumab)
Generic name Atezolizumab Pertuzumab
Indications Urothelial carcinoma, non-small cell lung cancer, triple-negative breast cancer HER2-positive breast cancer
Mechanism of action PD-L1 inhibitor HER2 dimerization inhibitor
Brand names Tecentriq Perjeta
Administrative route Intravenous infusion Intravenous infusion
Side effects Fatigue, nausea, cough, shortness of breath, decreased appetite Diarrhea, hair loss, nausea, fatigue, rash
Contraindications None known None known
Drug class Monoclonal antibody, Immune checkpoint inhibitor Monoclonal antibody, HER2 inhibitor
Manufacturer Genentech (Roche) Genentech (Roche)

Efficacy

Efficacy of Tecentriq (Atezolizumab) in Breast Cancer

Tecentriq (Atezolizumab) is an immune checkpoint inhibitor that has shown efficacy in the treatment of certain types of breast cancer. Atezolizumab works by targeting the programmed death-ligand 1 (PD-L1), thereby enhancing the body's immune response against cancer cells. Its efficacy in breast cancer was notably demonstrated in the IMpassion130 trial, a phase III study that focused on patients with unresectable locally advanced or metastatic triple-negative breast cancer (TNBC) that expressed PD-L1. In this study, the combination of atezolizumab and nab-paclitaxel significantly extended progression-free survival compared to placebo plus nab-paclitaxel. Furthermore, the combination therapy showed a meaningful improvement in overall survival in the PD-L1 positive population.

Efficacy of Perjeta (Pertuzumab) in Breast Cancer

Perjeta (Pertuzumab) is a monoclonal antibody that targets the HER2 receptor, a protein overexpressed in some forms of breast cancer. Pertuzumab is designed to prevent the HER2 receptor from pairing with other HER receptors on the surface of cancer cells, a process that is important for tumor growth and survival. The efficacy of pertuzumab in breast cancer has been established through several clinical trials, most notably the CLEOPATRA study. This phase III trial demonstrated that the addition of pertuzumab to trastuzumab and docetaxel chemotherapy significantly improved progression-free survival and overall survival in patients with HER2-positive metastatic breast cancer.

Combination Therapy in Breast Cancer

The combination of Tecentriq and Perjeta, along with other agents, has been explored in the treatment of breast cancer. The combination aims to leverage the different mechanisms of action—immune modulation by atezolizumab and HER2 blockade by pertuzumab—to enhance antitumor activity. Clinical trials such as the IMpassion131 study have investigated the safety and efficacy of this combination in patients with PD-L1 positive, metastatic triple-negative breast cancer. However, it is important to note that results from such trials should be interpreted with caution, and further research is needed to fully understand the potential benefits and risks of this combination therapy in breast cancer.

Conclusion

Both Tecentriq and Perjeta have shown significant efficacy in the treatment of specific subtypes of breast cancer. Tecentriq has been effective in PD-L1 positive triple-negative breast cancer, while Perjeta has improved outcomes in HER2-positive metastatic breast cancer. While the combination of these drugs represents a promising therapeutic strategy, it is crucial that their use is guided by clinical evidence and the individual patient's disease characteristics. Ongoing research and clinical trials continue to refine the understanding of how best to employ these agents in the complex landscape of breast cancer treatment.

Regulatory Agency Approvals

Tecentriq
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Perjeta
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)

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If Tecentriq or Perjeta 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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