Tecentriq (Atezolizumab) vs Piqray (alpelisib)

Tecentriq (Atezolizumab) vs Piqray (alpelisib)

Tecentriq (atezolizumab) is an immune checkpoint inhibitor that works by blocking the protein PD-L1, which is involved in suppressing the immune system's response to cancer cells, making it particularly useful in treating certain types of lung cancer, bladder cancer, and triple-negative breast cancer. Piqray (alpelisib), on the other hand, is a PI3K inhibitor that targets a specific genetic mutation (PIK3CA) and is used in combination with fulvestrant for the treatment of HR-positive, HER2-negative, PIK3CA-mutated, advanced or metastatic breast cancer after progression on or after an endocrine-based regimen. When deciding between Tecentriq and Piqray, it is crucial to consider the type of cancer, the presence of specific biomarkers (such as PD-L1 expression or PIK3CA mutation), and the overall treatment goals, as these medications are not interchangeable and are tailored to target different mechanisms of cancer growth.

Difference between Tecentriq and Piqray

Metric Tecentriq (Atezolizumab) Piqray (alpelisib)
Generic name Atezolizumab Alpelisib
Indications Urothelial carcinoma, non-small cell lung cancer, triple-negative breast cancer, small cell lung cancer, hepatocellular carcinoma Advanced or metastatic breast cancer with a PIK3CA mutation
Mechanism of action PD-L1 inhibitor, enhances T-cell function to better target and kill cancer cells PI3K inhibitor, targets the PI3K pathway in cancer cells
Brand names Tecentriq Piqray
Administrative route Intravenous infusion Oral
Side effects Fatigue, decreased appetite, nausea, urinary tract infections, fever, etc. Hyperglycemia, rash, diarrhea, decreased appetite, nausea, etc.
Contraindications Individuals with known hypersensitivity to atezolizumab or any of its components Individuals with severe hypersensitivity to alpelisib or any of its components
Drug class Monoclonal antibody, Immune checkpoint inhibitor Kinase inhibitor
Manufacturer Genentech (Roche) Novartis

Efficacy

Tecentriq (Atezolizumab) in Breast Cancer

Tecentriq (atezolizumab) is an immune checkpoint inhibitor that has shown efficacy in the treatment of triple-negative breast cancer (TNBC), a particularly aggressive form of the disease that does not express estrogen receptors, progesterone receptors, or excessive HER2 protein. Tecentriq targets the PD-L1 protein, which can be expressed on the surface of cancer cells or immune cells in the tumor environment. By blocking PD-L1, Tecentriq may help to restore the body’s immune response against cancer cells. In clinical trials, Tecentriq has been evaluated in combination with chemotherapy and has demonstrated an improvement in progression-free survival in patients with PD-L1-positive, metastatic TNBC. This has led to its approval by regulatory agencies for use in this specific patient population.

Piqray (Alpelisib) in Breast Cancer

Piqray (alpelisib) is a targeted therapy that has been approved for use in combination with fulvestrant for the treatment of hormone receptor-positive, human epidermal growth factor receptor 2 (HER2)-negative, PIK3CA-mutated, advanced or metastatic breast cancer. Alpelisib specifically inhibits the PIK3CA gene mutation, which is present in a subset of breast cancer patients and is associated with tumor growth, resistance to endocrine therapy, and a poor prognosis. Clinical trials have shown that Piqray, when used in conjunction with fulvestrant, significantly extends progression-free survival compared to fulvestrant alone in this patient population. This efficacy has led to its use as a standard treatment option for patients with this specific genetic mutation.

Comparative Efficacy in Breast Cancer

While both Tecentriq and Piqray have shown efficacy in breast cancer, their applications are tailored to specific subtypes of the disease. Tecentriq is effective in the treatment of PD-L1-positive TNBC, a form of cancer that lacks targeted hormone therapies. On the other hand, Piqray is effective in treating hormone receptor-positive, HER2-negative breast cancer with a PIK3CA mutation. The efficacy of these drugs highlights the importance of personalized medicine and the use of biomarkers to guide therapy in breast cancer. Patients are selected for treatment with Tecentriq or Piqray based on the presence of PD-L1 expression and PIK3CA mutations, respectively, ensuring that the right patients receive the most appropriate targeted therapy.

Conclusion

The introduction of drugs like Tecentriq and Piqray has advanced the treatment landscape for breast cancer by offering new options for patients with specific tumor characteristics. Their efficacy in improving outcomes for certain populations of breast cancer patients underscores the movement towards more personalized, targeted cancer therapies. As research continues, the efficacy of these drugs may be further defined, and their use may expand to other settings or in combination with other treatments to improve patient care in breast cancer.

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)
Piqray
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

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If Tecentriq or Piqray 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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