EGFR mutation and resistance of non-small-cell lung cancer to gefitinib

被引:3319
作者
Kobayashi, S
Boggon, TJ
Dayaram, T
Janne, PA
Kocher, O
Meyerson, M
Johnson, BE
Eck, MJ
Tenen, DG
Halmos, B
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Div Hematol Oncol, Boston, MA 02215 USA
[2] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Pathol, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA
[6] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[7] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med, Boston, MA 02115 USA
[8] Case Western Reserve Univ, Univ Hosp Cleveland, Case Sch Med, Ireland Canc Ctr, Cleveland, OH 44106 USA
关键词
D O I
10.1056/NEJMoa044238
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mutations of the epidermal growth factor receptor ( EGFR) gene have been identified in from patients with non-small-cell lung cancer who have a response to anilinoquinazoline EGFR inhibitors. Despite the dramatic responses to such inhibitors, patients ultimately have a relapse. The mechanism of the drug resistance is unknown. Here we report the case of a patient with EGFR - mutant, gefitinib-responsive, non-small-cell lung cancer who had a relapse after two years of complete remission during treatment with gefitinib. The DNA sequence of the EGFR gene in his biopsy specimen at relapse revealed the presence of a second point mutation, resulting in threonine-to-methionine amino acid change at position 790 of EGFR. Structural modeling and biochemical studies showed that this second mutation led to gefitinib resistance.
引用
收藏
页码:786 / 792
页数:7
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