Alecensa (alectinib) vs Lorviqua (lorlatinib)

Alecensa (alectinib) vs Lorviqua (lorlatinib)

Alecensa (alectinib) and Lorviqua (lorlatinib) are both oral medications used to treat ALK-positive non-small cell lung cancer (NSCLC), but they differ in their generation and specificity. Alecensa, a second-generation ALK inhibitor, is often used as a first-line treatment and is known for its effectiveness in controlling brain metastases. In contrast, Lorviqua is a third-generation ALK inhibitor that can be used in patients who have developed resistance to earlier ALK inhibitors, offering a potential treatment option for those with more advanced disease stages or after other therapies have failed.

Difference between Alecensa and Lorviqua

Metric Alecensa (alectinib) Lorviqua (lorlatinib)
Generic name Alectinib Lorlatinib
Indications ALK-positive metastatic non-small cell lung cancer (NSCLC) ALK-positive metastatic NSCLC
Mechanism of action ALK inhibitor ALK and ROS1 inhibitor
Brand names Alecensa Lorviqua
Administrative route Oral Oral
Side effects Fatigue, constipation, edema, myalgia Hypercholesterolemia, neuropathy, edema, weight gain
Contraindications Hypersensitivity to alectinib Hypersensitivity to lorlatinib
Drug class Tyrosine kinase inhibitor Tyrosine kinase inhibitor
Manufacturer Genentech (Roche) Pfizer

Efficacy

Alecensa (Alectinib) Efficacy in Lung Cancer

Alecensa (alectinib) is a targeted therapy approved for the treatment of non-small cell lung cancer (NSCLC) with specific genetic mutations. It is an ALK inhibitor designed to target and inhibit the activity of the anaplastic lymphoma kinase (ALK), which can drive the growth of cancer cells. In clinical trials, alectinib has demonstrated significant efficacy in patients with ALK-positive NSCLC. It has been shown to improve progression-free survival (PFS) when compared to crizotinib, another ALK inhibitor, in the first-line setting. Moreover, alectinib has been associated with high rates of intracranial response in patients with brain metastases, a common complication of advanced NSCLC.

In the ALEX trial, a phase III study comparing alectinib to crizotinib in previously untreated ALK-positive NSCLC, alectinib significantly reduced the risk of disease progression or death by 53% compared to crizotinib. Additionally, the median PFS for patients treated with alectinib was not reached at the time of analysis, indicating a prolonged period of disease control. This study established alectinib as a preferred first-line treatment option for patients with ALK-positive NSCLC.

Lorviqua (Lorlatinib) Efficacy in Lung Cancer

Lorviqua (lorlatinib) is another ALK inhibitor indicated for the treatment of patients with ALK-positive metastatic NSCLC. It is generally used in patients who have progressed on prior ALK inhibitors, such as crizotinib, ceritinib, or alectinib. Lorlatinib has been designed to overcome resistance to earlier-generation ALK inhibitors and has a unique ability to penetrate the blood-brain barrier effectively, which is crucial for treating brain metastases.

In clinical trials, lorlatinib has shown substantial efficacy in patients who have failed previous ALK inhibitors. The objective response rate (ORR) in patients treated with lorlatinib was significant, with many patients achieving partial or complete responses. The median duration of response (DOR) was also notable, suggesting that lorlatinib can provide lasting benefits for patients with ALK-positive NSCLC. These results support the use of lorlatinib as a treatment for patients with ALK-positive NSCLC who have progressed on other ALK-targeted therapies.

Regulatory Agency Approvals

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

Access Alecensa or Lorviqua today

If Alecensa or Lorviqua 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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