Imfinzi (durvalumab) vs Alecensa (alectinib)

Imfinzi (durvalumab) vs Alecensa (alectinib)

Imfinzi (durvalumab) is an immune checkpoint inhibitor specifically targeting the PD-L1 protein, used primarily in the treatment of certain types of urothelial carcinoma and non-small cell lung cancer (NSCLC). Alecensa (alectinib) is a tyrosine kinase inhibitor that targets the ALK protein and is used to treat NSCLC in patients who have ALK mutations. The choice between Imfinzi and Alecensa would depend on the specific genetic markers and characteristics of the patient's cancer, as well as the overall health profile of the patient, which should be thoroughly discussed with an oncologist.

Difference between Imfinzi and Alecensa

Metric Imfinzi (durvalumab) Alecensa (alectinib)
Generic name Durvalumab Alectinib
Indications Urothelial carcinoma, non-small cell lung cancer (NSCLC) Non-small cell lung cancer (NSCLC), specifically ALK-positive
Mechanism of action PD-L1 inhibitor ALK inhibitor
Brand names Imfinzi Alecensa
Administrative route Intravenous infusion Oral
Side effects Fatigue, musculoskeletal pain, constipation, decreased appetite, nausea, peripheral edema, urinary tract infection, fever, rash Constipation, fatigue, peripheral edema, myalgia, anemia, elevated liver enzymes, diarrhea, muscle pain, rash
Contraindications Hypersensitivity to durvalumab or any of its excipients Hypersensitivity to alectinib or any of its excipients, severe hepatic impairment
Drug class Antineoplastic, immune checkpoint inhibitor Antineoplastic, tyrosine kinase inhibitor
Manufacturer AstraZeneca Genentech (a member of the Roche Group)

Efficacy

Imfinzi (Durvalumab) Efficacy in Lung Cancer

Imfinzi (durvalumab) is a programmed death-ligand 1 (PD-L1) blocking antibody used in the treatment of lung cancer, specifically in the management of certain types of non-small cell lung cancer (NSCLC). Clinical trials have demonstrated its efficacy as a maintenance therapy in patients with stage III NSCLC who have not progressed following concurrent platinum-based chemotherapy and radiation therapy. The PACIFIC trial, a pivotal study for durvalumab, showed a significant improvement in median progression-free survival (PFS) compared to placebo. Furthermore, durvalumab treatment has also led to an improvement in overall survival (OS) in this patient population, marking it as a significant advancement in the management of stage III NSCLC.

For patients with advanced NSCLC whose tumors express PD-L1 on 1% or more of tumor cells, durvalumab is indicated as a first-line treatment in combination with etoposide and either carboplatin or cisplatin. The efficacy of durvalumab in this setting is supported by improved survival outcomes and response rates when used as part of a combination regimen, as shown in clinical studies. However, it is important to note that the efficacy of durvalumab can vary based on the level of PD-L1 expression and the presence of specific genetic mutations.

Alecensa (Alectinib) Efficacy in Lung Cancer

Alecensa (alectinib) is a tyrosine kinase inhibitor specifically designed to target the anaplastic lymphoma kinase (ALK) fusion gene, which is a driver of oncogenesis in a subset of NSCLC patients. Alectinib has demonstrated high efficacy in patients with ALK-positive NSCLC, both in the first-line setting and after progression on crizotinib, which was the first ALK inhibitor approved for this indication. In clinical trials, alectinib has shown a prolonged PFS compared to crizotinib, with the ALEX trial being a landmark study that established alectinib as a preferred first-line treatment for ALK-positive NSCLC patients.

Moreover, alectinib has a notable ability to penetrate the central nervous system (CNS), which is particularly important as the brain is a common site of metastasis for ALK-positive NSCLC. Clinical data have shown that alectinib significantly reduces the risk of CNS progression and is associated with high rates of CNS response in patients with brain metastases. The efficacy of alectinib in controlling disease both systemically and in the CNS makes it a critical option for patients with ALK-positive NSCLC, potentially altering the course of the disease and improving patient outcomes.

Regulatory Agency Approvals

Imfinzi
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Alecensa
  • 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)

Access Imfinzi or Alecensa today

If Imfinzi or Alecensa 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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