GRCh38 · COSMIC v94

Summary

This section shows a summary for the selected study (COSU identifier) or publication (COSP identifier). Studies may have been performed by the Sanger Institute Cancer Genome Project, or imported from the ICGC/TCGA. You can see more information on the help pages.

Reference
Sequential ALK Inhibitors Can Select for Lorlatinib-Resistant Compound ALK Mutations in ALK-Positive Lung Cancer.
Paper ID
COSP47670
Authors
Yoda S, Lin JJ, Lawrence MS, Burke BJ, Friboulet L, Langenbucher A, Dardaei L, Prutisto-Chang K, Dagogo-Jack I, Timofeevski S, Hubbeling H, Gainor JF, Ferris LA, Riley AK, Kattermann KE, Timonina D, Heist RS, Iafrate AJ, Benes CH, Lennerz JK, Mino-Kenudson M, Engelman JA, Johnson TW, Hata AN and Shaw AT
Affiliation
Massachusetts General Hospital Cancer Center, Charlestown, Massachusetts.
Journal
Cancer discovery, 2018;8(6):714-729
ISSN: 2159-8290
PMID: 29650534 (view at PubMed or Europe PMC)
Abstract
The cornerstone of treatment for advanced ALK-positive lung cancer is sequential therapy with increasingly potent and selective ALK inhibitors. The third-generation ALK inhibitor lorlatinib has demonstrated clinical activity in patients who failed previous ALK inhibitors. To define the spectrum of <i>ALK</i> mutations that confer lorlatinib resistance, we performed accelerated mutagenesis screening of Ba/F3 cells expressing EML4-ALK. Under comparable conditions, <i>N</i>-ethyl-<i>N</i>-nitrosourea (ENU) mutagenesis generated numerous crizotinib-resistant but no lorlatinib-resistant clones harboring single <i>ALK</i> mutations. In similar screens with EML4-ALK containing single <i>ALK</i> resistance mutations, numerous lorlatinib-resistant clones emerged harboring compound <i>ALK</i> mutations. To determine the clinical relevance of these mutations, we analyzed repeat biopsies from lorlatinib-resistant patients. Seven of 20 samples (35%) harbored compound <i>ALK</i> mutations, including two identified in the ENU screen. Whole-exome sequencing in three cases confirmed the stepwise accumulation of <i>ALK</i> mutations during sequential treatment. These results suggest that sequential ALK inhibitors can foster the emergence of compound <i>ALK</i> mutations, identification of which is critical to informing drug design and developing effective therapeutic strategies.<b>Significance:</b> Treatment with sequential first-, second-, and third-generation ALK inhibitors can select for compound <i>ALK</i> mutations that confer high-level resistance to ALK-targeted therapies. A more efficacious long-term strategy may be up-front treatment with a third-generation ALK inhibitor to prevent the emergence of on-target resistance. <i>Cancer Discov; 8(6); 714-29. ©2018 AACR.</i><i>This article is highlighted in the In This Issue feature, p. 663</i>.
Paper Status
Curated