Posts tagged progression
A phase II study of lorlatinib in patients (pts) with ALK-positive (ALK+) lung cancer with brain-only progression

Background: Lorlatinib is a 3rd-generation ALK tyrosine kinase inhibitor (TKI) developed to penetrate the central nervous system (CNS) and overcome resistance to 2nd-generation (2nd-gen) ALK TKIs. In a phase II study, lorlatinib demonstrated significant intracranial (IC) activity after failure of 2nd-gen TKIs. As treatment discontinuation for extracranial (EC) progression can confound assessment of durability of IC response, we performed a phase II study (NCT02927340) to selectively evaluate lorlatinib activity in ALK+ pts with CNS-only disease... Conclusions: Lorlatinib induces durable intracranial responses in pts with CNS-only progression on 2nd-gen ALK TKIs, suggesting that CNS-specific relapses are primarily driven by ALK-dependent mechanisms. Further studies are needed to characterize the molecular basis of sensitivity to lorlatinib in this unique subgroup of pts with ALK+ lung cancer. Clinical trial information: NCT02927340 READ ARTICLE

Journal of Clinical Oncology DOI:10.1200/JCO.2020.38.15_suppl.9595

Authors: Ibiayi Dagogo-Jack, Geoffrey R. Oxnard, Jessica Fink, Gianluca Diubaldi, Caitlyn Helms, Justin F. Gainor, Michael S. Rabin, Rebecca Suk Heist, Jessica Jiyeong Lin, Jennifer Ackil, Alona Muzikansky, Alice Tsang Shaw

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Brain Penetration of Lorlatinib: Cumulative Incidences of CNS and Non-CNS Progression with Lorlatinib in Patients with Previously Treated ALK-Positive Non-Small-Cell Lung Cancer

Lorlatinib is a potent, brain-penetrant, third-generation ALK/ROS1 TKI. We performed an analysis of CNS and non-CNS progression in patients with pretreated ALK+ NSCLC. Our results indicate that lorlatinib is active in the treatment and prevention of CNS metastases in patients with ALK+ NSCLC, including those who had progressed on crizotinib or second-generation TKIs. READ ARTICLE

Targeted Oncology Volume DOI:10.1007/s11523-020-00702-4

Authors: Bauer, T.M., Shaw, A.T., Johnson, M.L. et al.

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