<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(1)</volume><submitter>Zhang Y</submitter><pubmed_abstract>This retrospective study investigated the association between the pattern of disease progression and molecular mechanism of acquired resistance in a large cohort of 49 patients with ROS1-rearranged advanced non-small-cell lung cancer treated with first-line crizotinib. We found that treatment-emergent ROS1 point mutations were the major molecular mechanism of crizotinib resistance, particularly for patients who developed extracranial-only disease progression. Our findings highlight the importance of rebiopsy and gene testing for subsequent-line therapeutic management.</pubmed_abstract><journal>NPJ precision oncology</journal><pagination>20</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8971474</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Disease progression patterns and molecular resistance mechanisms to crizotinib of lung adenocarcinoma harboring ROS1 rearrangements.</pubmed_title><pmcid>PMC8971474</pmcid><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Lizaso A</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Zeng L</pubmed_authors><pubmed_authors>Yang N</pubmed_authors><pubmed_authors>Xu Q</pubmed_authors><pubmed_authors>Xu C</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Huang Z</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Song Z</pubmed_authors><pubmed_authors>Ou SI</pubmed_authors></additional><is_claimable>false</is_claimable><name>Disease progression patterns and molecular resistance mechanisms to crizotinib of lung adenocarcinoma harboring ROS1 rearrangements.</name><description>This retrospective study investigated the association between the pattern of disease progression and molecular mechanism of acquired resistance in a large cohort of 49 patients with ROS1-rearranged advanced non-small-cell lung cancer treated with first-line crizotinib. We found that treatment-emergent ROS1 point mutations were the major molecular mechanism of crizotinib resistance, particularly for patients who developed extracranial-only disease progression. Our findings highlight the importance of rebiopsy and gene testing for subsequent-line therapeutic management.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-19T17:38:05.283Z</modification><creation>2025-04-19T17:38:05.283Z</creation></dates><accession>S-EPMC8971474</accession><cross_references><pubmed>35361870</pubmed><doi>10.1038/s41698-022-00264-w</doi></cross_references></HashMap>