Tecentriq (Atezolizumab) vs Augtyro (repotrectinib)

Tecentriq (Atezolizumab) vs Augtyro (repotrectinib)

Tecentriq (Atezolizumab) is an immune checkpoint inhibitor used primarily to treat certain types of urinary bladder, lung, breast, and liver cancers by helping the immune system recognize and attack cancer cells. Augtyro (repotrectinib), on the other hand, is a tyrosine kinase inhibitor that targets specific genetic mutations and is used to treat cancers such as non-small cell lung cancer (NSCLC) and solid tumors with a neurotrophic tyrosine receptor kinase (NTRK) gene fusion. When deciding between Tecentriq and Augtyro, it is crucial to consider the specific type of cancer, its genetic makeup, and the patient's overall health, as each medication targets different pathways and mechanisms within the cancer cells.

Difference between Tecentriq and Augtyro

Metric Tecentriq (Atezolizumab) Augtyro (repotrectinib)
Generic name Atezolizumab Repotrectinib
Indications Urothelial carcinoma, non-small cell lung cancer, triple-negative breast cancer Advanced solid tumors with NTRK or ROS1 gene fusions
Mechanism of action PD-L1 inhibitor, immune checkpoint inhibitor Tyrosine kinase inhibitor
Brand names Tecentriq Augtyro
Administrative route Intravenous Oral
Side effects Fatigue, nausea, decreased appetite, urinary tract infections, fever Dizziness, constipation, fatigue, edema, myalgia
Contraindications None known specifically; caution in patients with autoimmune disease or prior organ transplantation None known specifically; caution in patients with QT prolongation
Drug class Monoclonal antibody, Immune checkpoint inhibitor Tyrosine kinase inhibitor
Manufacturer Genentech (Roche) Turning Point Therapeutics

Efficacy

Tecentriq (Atezolizumab) Efficacy in Lung Cancer

Tecentriq (Atezolizumab) is a programmed death-ligand 1 (PD-L1) blocking antibody used in the treatment of various types of cancer, including lung cancer. Specifically, for non-small cell lung cancer (NSCLC), Tecentriq has been shown to be effective as both a monotherapy and in combination with chemotherapy. Clinical trials have demonstrated that Tecentriq can significantly improve overall survival and progression-free survival in patients with NSCLC compared to chemotherapy alone. The efficacy of Tecentriq is particularly notable in patients whose tumors express PD-L1, as the blockade of this pathway helps to activate the immune system to target and destroy cancer cells.

When used as a first-line treatment for metastatic NSCLC, Tecentriq, in combination with chemotherapy, has shown a substantial benefit in extending the lives of patients without their disease worsening. This combination has become a standard of care for patients with advanced lung cancer without targetable genetic mutations. The efficacy of Tecentriq has also been established in the treatment of small cell lung cancer (SCLC), with improvements in survival outcomes when added to the standard chemotherapy regimen.

Augtyro (Repotrectinib) Efficacy in Lung Cancer

Augtyro (Repotrectinib) is an investigational, next-generation tyrosine kinase inhibitor (TKI) that targets the tropomyosin receptor kinase (TRK), ROS1, and anaplastic lymphoma kinase (ALK) fusion proteins. It is being studied for its efficacy in treating non-small cell lung cancer (NSCLC) with these specific genetic alterations. Early clinical trials have shown promising results, indicating that repotrectinib has potent anti-tumor activity in NSCLC patients with ROS1 or NTRK fusions, particularly in those who have developed resistance to prior therapies targeting these mutations.

Repotrectinib's design allows for the targeting of resistance mutations that can develop after treatment with earlier-generation TKIs. This feature potentially offers an effective treatment option for patients who have limited alternatives due to resistance. While the data is still emerging, the results suggest that repotrectinib could provide a new line of therapy for NSCLC patients with specific genetic profiles. It is important to note that as of the knowledge cutoff date, repotrectinib is still under clinical investigation and has not yet received approval from regulatory agencies for the treatment of lung cancer or any other indication.

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)
Augtyro
  • Food and Drug Administration (FDA), USA

Access Tecentriq or Augtyro today

If Tecentriq or Augtyro 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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