FDA Approves Alectinib for Early-Stage ALK+ NSCLC

News
Article

The FDA has approved alectinib for the adjuvant treatment of patients with ALK-positive non-small cell lung cancer with tumors that are least 4 cm or node positive, as detected by an FDA-approved test.

FDA

FDA

The FDA has approved alectinib (Alecensa) for the adjuvant treatment of patients with ALK-positive non-small cell lung cancer (NSCLC) with tumors that are at least 4 cm or node-positive, as detected by an FDA-approved test.

The approval is based on results from the phase 3 ALINA trial (NCT0346076) assessing alectinib vs chemotherapy for patients with early-stage ALK-positive NSCLC. The risk of death or recurrence was reduced by 76% (HR, 0.24; 95% CI, 0.13-0.43; P <.0001). The disease-free survival (DFS) was also observed in an exploratory analysis and saw an improvement (HR, 0.22; 95% CI, 0.08-0.58).

“The approval of [alectinib] marks a pivotal moment for [patients with] newly diagnosed with early-stage ALK-positive lung cancer, who until now, were not able to receive ALK-specific therapy,” said Ken Culver, director of Research and Clinical Affairs at ALK Positive, Inc. “These patients, who are typically diagnosed at a younger age, often face recurrence and have a higher risk of developing brain metastases than those with other types of NSCLC. Now, with this significant advance, it is more important than ever that all people diagnosed with early-stage lung cancer undergo testing for ALK and other recommended biomarkers to receive the treatment most appropriate for them.”

The study enrolled 257 patients who were randomly assigned to receive either alectinib or chemotherapy. The primary end point was DFS and secondary end points included overall survival, central nervous system DFS, and the amount of patients with adverse effects.

Alectinib was designed to prevent lung cancer occurrence after it had been removed by surgery, or to treat patients where the tumor has metastasized.

References

  1. FDA approves Genentech's Alecensa as first adjuvant treatment for people with ALK-positive early-stage lung cancer. News release. Genentech. April 18, 2024. Accessed April 18, 2024. https://shorturl.at/zSV29
  2. Wu YL, Dziadziuszko R, Ahn JS, et al. Alectinib in resected ALK-positive non-small-cell lung cancer. N Engl J Med. 2024;390(14):1265-1276. doi:10.1056/NEJMoa2310532
Recent Videos
The 2 main pafolacianine components, a folate analog and a dye, are commonly used in other medical applications.
An intravenous infusion administered prior to surgery enables treatment to occur in a normal time frame without the need for additional procedural time.
The FirstLook liquid biopsy, when used as an adjunct to low-dose CT, may help to address the unmet need of low lung cancer screening utilization.
An 80% sensitivity for lung cancer was observed with the liquid biopsy, with high sensitivity observed for early-stage disease, as well.
Patients who face smoking stigma, perceive a lack of insurance, or have other low-dose CT related concerns may benefit from blood testing for lung cancer.
Patrick Oh, MD, highlights next steps for further research in treating patients with systemic therapy in addition to radiotherapy for early-stage NSCLC.
Increased use of systemic therapies, particularly among patients with high-risk node-negative NSCLC, were observed following radiotherapy.
Interest in novel therapies to improve outcomes initiated an investigation of the use of immunotherapy in early-stage non-small cell lung cancer.
Higher, durable rates of response to frontline therapy are needed to potentially improve long-term survival among patients with non–small cell lung cancer.
Martin Dietrich, MD, PhD, and Wade T. Iams, MD, experts on lung cancer
Related Content