Tecentriq (Atezolizumab) vs Enhertu (fam-trastuzumab deruxtecan-nxki)

Tecentriq (Atezolizumab) vs Enhertu (fam-trastuzumab deruxtecan-nxki)

Tecentriq (Atezolizumab) is an immune checkpoint inhibitor that works by blocking the protein PD-L1, which is involved in suppressing the immune response against cancer cells, and is commonly used in the treatment of various types of cancers such as lung cancer, bladder cancer, and triple-negative breast cancer. On the other hand, Enhertu (fam-trastuzumab deruxtecan-nxki) is an antibody-drug conjugate that targets HER2-positive cancer cells, releasing a chemotherapy agent directly into them, and is primarily used for the treatment of HER2-positive breast cancer and gastric cancer. The right medicine for a patient would depend on the specific type of cancer they have, its molecular profile, including PD-L1 or HER2 expression, and the overall treatment plan determined by a healthcare professional.

Difference between Tecentriq and Enhertu

Metric Tecentriq (Atezolizumab) Enhertu (fam-trastuzumab deruxtecan-nxki)
Generic name Atezolizumab fam-trastuzumab deruxtecan-nxki
Indications Urothelial carcinoma, non-small cell lung cancer, triple-negative breast cancer HER2-positive breast cancer, HER2-positive gastric cancer
Mechanism of action PD-L1 inhibitor, immunotherapy HER2-directed antibody and topoisomerase inhibitor conjugate
Brand names Tecentriq Enhertu
Administrative route Intravenous infusion Intravenous infusion
Side effects Fatigue, decreased appetite, nausea, urinary tract infections, fever Nausea, fatigue, vomiting, alopecia, constipation
Contraindications None known None known
Drug class Monoclonal antibody, PD-L1 blocking antibody Antibody-drug conjugate
Manufacturer Genentech (Roche) Daiichi Sankyo and AstraZeneca

Efficacy

Efficacy of Tecentriq (Atezolizumab) in Lung Cancer

Tecentriq (Atezolizumab) is a monoclonal antibody designed to bind with the programmed death-ligand 1 (PD-L1), which is expressed on tumor cells and tumor-infiltrating immune cells. By blocking the interaction between PD-L1 and its receptors PD-1 and B7.1, Tecentriq may enable the activation of T cells, which can then attack the cancer cells. In non-small cell lung cancer (NSCLC), Tecentriq has shown efficacy as both a monotherapy and in combination with other treatments. In particular, it has been approved for use in patients with metastatic NSCLC with high PD-L1 expression and no EGFR or ALK genomic tumor aberrations, demonstrating improvements in overall survival compared to chemotherapy alone.

Additionally, Tecentriq has been studied in small cell lung cancer (SCLC). It has been approved for use in combination with carboplatin and etoposide for the first-line treatment of adults with extensive-stage SCLC. Clinical trials have shown that this combination can lead to a significant improvement in overall survival and progression-free survival when compared to chemotherapy alone. This marks a notable advancement in the treatment of a particularly aggressive form of lung cancer.

Efficacy of Enhertu (fam-trastuzumab deruxtecan-nxki) in Lung Cancer

Enhertu (fam-trastuzumab deruxtecan-nxki) is an antibody-drug conjugate consisting of a humanized anti-HER2 antibody, a stable linker, and a cytotoxic topoisomerase I inhibitor payload. It is designed to target and deliver chemotherapy directly to cancer cells that overexpress HER2. While traditionally associated with breast cancer, HER2 mutations are also present in a subset of non-small cell lung cancers (NSCLC). Enhertu has shown promising results in patients with HER2-mutant NSCLC. In clinical studies, patients treated with Enhertu demonstrated a significant response rate, with many experiencing tumor shrinkage. This has provided a new treatment avenue for patients with this specific molecular alteration in lung cancer.

The efficacy of Enhertu in lung cancer patients with HER2 overexpression or mutations suggests a potential shift in the treatment landscape for this challenging disease. As a targeted therapy, Enhertu offers a more personalized approach to cancer treatment, which is particularly valuable in lung cancer where the molecular profile of the tumor can significantly influence the choice and success of treatment. Ongoing clinical trials continue to evaluate the long-term benefits and optimal use of Enhertu in various settings of lung cancer care.

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)
Enhertu
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Access Tecentriq or Enhertu today

If Tecentriq or Enhertu 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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