Alectinib continuation beyond progression in ALK-positive non-small cell lung cancer with alectinib-refractory

Yimeng Li1, Zhanpeng Hao1, Yuyan Ma1

  • 1Department of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

PubMed
Abstract

Insights

Continuing alectinib with other therapies shows promise for ALK-positive NSCLC patients who develop resistance. This approach may improve survival outcomes compared to switching treatments after disease progression.

Area of Science:

  • Oncology
  • Pharmacology

Background:

  • Alectinib is a key treatment for anaplastic lymphoma kinase-positive non-small cell lung cancer (NSCLC).
  • A significant percentage of patients develop resistance to alectinib, necessitating further treatment strategies.
  • Limited data exists on continuing alectinib post-progression in NSCLC.

Purpose of the Study:

  • To evaluate the efficacy and safety of continuing alectinib combined with other therapies after disease progression in ALK-positive NSCLC patients.
  • To identify potential patient populations who may benefit from this strategy.

Main Methods:

  • Retrospective cohort study of 15 patients with ALK-positive NSCLC in China (2019-2022).
  • Patients received continued alectinib plus other therapies after oligoprogression or central nervous system (CNS) progression.
  • Evaluated outcomes included median progression-free survival (mPFS), objective response rate (ORR), median overall survival (mOS), and adverse events (AEs).

Main Results:

  • Continued alectinib treatment demonstrated a median PFS of 8 months (95% CI: 4 to NA).
  • The objective response rate (ORR) was 46.7% in the studied cohort.
  • Adverse events were minimal, with only one patient experiencing Grade 2 liver enzyme elevation.

Conclusions:

  • Continuing alectinib with other therapies is effective and safe for ALK-positive NSCLC patients with oligoprogression or CNS progression.
  • This strategy may offer superior survival benefits compared to immediate switching to alternative ALK-TKIs.