Lorlatinib in advanced ALK-positive NSCLC after prior progression on ALK inhibitors: real-world experience in Russia

Sergey V Orlov1,2,3, Konstantin K Laktionov4, Aram A Musaelyan1,2,3

  • 1Department of Clinical Oncology, Pavlov First Saint Petersburg State Medical University, St. Petersburg 197022, Russia.

Abstract

Insights

Lorlatinib shows significant efficacy in patients with ALK-rearranged metastatic non-small cell lung cancer (NSCLC) progressing on prior tyrosine kinase inhibitors (TKIs). Long-term responders to previous therapies experienced notably extended progression-free and overall survival with lorlatinib treatment.

Area of Science:

  • Oncology
  • Pharmacology
  • Clinical Trials

Background:

  • Anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer (NSCLC) often requires sequential tyrosine kinase inhibitor (TKI) therapy.
  • Resistance to early-generation ALK TKIs necessitates evaluation of subsequent treatment options like lorlatinib.
  • Real-world data is crucial for understanding the effectiveness and safety of lorlatinib in diverse patient populations.

Purpose of the Study:

  • To assess the real-world effectiveness and safety of lorlatinib in patients with ALK-rearranged metastatic NSCLC.
  • To evaluate lorlatinib's efficacy in patients who have previously failed at least one ALK TKI.
  • To identify factors influencing outcomes in patients treated with lorlatinib after progression on prior therapies.

Main Methods:

  • Retrospective analysis of 82 patients with metastatic NSCLC treated with lorlatinib.
  • Inclusion criteria: ALK rearrangement, prior TKI failure, and progression.
  • Data collected on objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and adverse events (AEs).

Main Results:

  • Overall ORR was 64.6% and DCR was 96.3%.
  • Intracranial ORR and DCR were 66.2% and 96.9% in patients with brain metastases.
  • Median PFS was 66.7 months; median OS was not reached. Patients with >12 months prior TKI benefit had significantly longer PFS and OS.
  • Prior response duration to ALK TKI <12 months was an independent negative predictor of survival.

Conclusions:

  • Lorlatinib demonstrates substantial benefit in selected patients with ALK-rearranged NSCLC progressing on prior TKIs, particularly long-term responders.
  • The study highlights the importance of prior treatment response duration as a predictor of lorlatinib efficacy.
  • Findings emphasize the need for careful patient selection, as generalizability to unselected populations may be limited.