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Acquired Resistance to Crizotinib from a Mutation in CD74ROS1
Author(s) -
Mark M. Awad,
Ryohei Katayama,
Michele McTigue,
Wei Liu,
Yali Deng,
Alexei Brooun,
Luc Friboulet,
Donghui Huang,
Matthew D. Falk,
Sergei Timofeevski,
Keith D. Wilner,
Elizabeth L. Lockerman,
Tahsin M. Khan,
Sidra Mahmood,
Justin F. Gainor,
Subba R. Digumarthy,
James R. Stone,
Mari MinoKenudson,
James G. Christensen,
A. John Iafrate,
Jeffrey A. Engelman,
Alice T. Shaw
Publication year - 2013
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1215530
Subject(s) - crizotinib , ros1 , anaplastic lymphoma kinase , medicine , cancer research , mutation , adenocarcinoma , alk inhibitor , lung cancer , genetics , oncology , cancer , biology , gene , malignant pleural effusion
Crizotinib, an inhibitor of anaplastic lymphoma kinase (ALK), has also recently shown efficacy in the treatment of lung cancers with ROS1 translocations. Resistance to crizotinib developed in a patient with metastatic lung adenocarcinoma harboring a CD74-ROS1 rearrangement who had initially shown a dramatic response to treatment. We performed a biopsy of a resistant tumor and identified an acquired mutation leading to a glycine-to-arginine substitution at codon 2032 in the ROS1 kinase domain. Although this mutation does not lie at the gatekeeper residue, it confers resistance to ROS1 kinase inhibition through steric interference with drug binding. The same resistance mutation was observed at all the metastatic sites that were examined at autopsy, suggesting that this mutation was an early event in the clonal evolution of resistance. (Funded by Pfizer and others; ClinicalTrials.gov number, NCT00585195.).

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