Portrazza (necitumumab) vs Alunbrig (brigatinib)

Portrazza (necitumumab) vs Alunbrig (brigatinib)

Portrazza (necitumumab) is a monoclonal antibody designed to target and block the epidermal growth factor receptor (EGFR), and is approved for use in combination with chemotherapy for the treatment of metastatic squamous non-small cell lung cancer (NSCLC) that has not responded to other treatments. Alunbrig (brigatinib), on the other hand, is a tyrosine kinase inhibitor that targets anaplastic lymphoma kinase (ALK) and is used for the treatment of NSCLC in patients who have an ALK mutation and have progressed on or are intolerant to crizotinib. The choice between Portrazza and Alunbrig would largely depend on the patient's specific type of NSCLC, as determined by biomarker testing, and the presence of either EGFR or ALK genetic alterations, respectively.

Difference between Portrazza and Alunbrig

Metric Portrazza (necitumumab) Alunbrig (brigatinib)
Generic name Necitumumab Brigatinib
Indications Metastatic squamous non-small cell lung cancer (NSCLC) Non-small cell lung cancer (NSCLC) with ALK-positive metastasis
Mechanism of action Epidermal growth factor receptor (EGFR) antagonist Anaplastic lymphoma kinase (ALK) inhibitor
Brand names Portrazza Alunbrig
Administrative route Intravenous infusion Oral
Side effects Rash, magnesium depletion, venous thromboembolism, dermatitis Nausea, diarrhea, fatigue, cough, headache
Contraindications Hypomagnesemia, hypersensitivity to necitumumab or its excipients Hypersensitivity to brigatinib or its excipients, pulmonary toxicity
Drug class Monoclonal antibody Tyrosine kinase inhibitor
Manufacturer Eli Lilly and Company Takeda Pharmaceutical Company

Efficacy

Portrazza (Necitumumab) Efficacy in Lung Cancer

Portrazza (necitumumab) is a monoclonal antibody used for the treatment of metastatic squamous non-small cell lung cancer (NSCLC). It targets the epidermal growth factor receptor (EGFR), which is often overexpressed in squamous NSCLC cells. The efficacy of necitumumab was evaluated in a pivotal phase III clinical trial known as SQUIRE. The study compared necitumumab in combination with chemotherapy (gemcitabine and cisplatin) to chemotherapy alone in patients with advanced squamous NSCLC. The results demonstrated a statistically significant improvement in overall survival for patients receiving necitumumab in addition to chemotherapy, with a median survival of 11.5 months compared to 9.9 months in the chemotherapy-only group.

However, it is important to note that the addition of necitumumab also led to an increase in certain side effects. Therefore, while Portrazza has shown efficacy in extending overall survival in the studied population, its use must be carefully considered against the potential for increased toxicity. Portrazza is specifically indicated for first-line treatment in combination with chemotherapy for patients with metastatic squamous NSCLC and is not indicated for other types of lung cancer.

Alunbrig (Brigatinib) Efficacy in Lung Cancer

Alunbrig (brigatinib) is a tyrosine kinase inhibitor (TKI) approved for the treatment of anaplastic lymphoma kinase-positive (ALK+) non-small cell lung cancer (NSCLC) in patients who have progressed on or are intolerant to crizotinib. Brigatinib has shown high efficacy in patients with ALK+ NSCLC, with a response rate significantly higher than what is typically observed with chemotherapy in this patient population. In the ALTA trial, brigatinib demonstrated an objective response rate (ORR) of 45% in patients previously treated with crizotinib. Additionally, the median progression-free survival (PFS) was 16.7 months, which is notable given that these patients had already progressed on prior ALK inhibitors.

Brigatinib also has activity in the central nervous system (CNS), which is particularly important as the brain is a common site for metastasis in ALK+ NSCLC. The intracranial ORR in the ALTA trial was 67% among patients with measurable brain metastases. Given these results, Alunbrig is considered an effective treatment option for patients with ALK+ NSCLC, especially for those who have failed previous ALK inhibitor therapy. Its efficacy in both systemic and CNS disease makes it a valuable agent in the management of this specific subtype of lung cancer.

Regulatory Agency Approvals

Portrazza
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
Alunbrig
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Access Portrazza or Alunbrig today

If Portrazza or Alunbrig 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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