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PMID: 18596266 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Detection of mutations in EGFR in circulating lung-cancer cells.

The New England journal of medicine ·Vol. 359 ·No. 4 ·2008-07-24 ·Pages 366-77

Maheswaran S, Sequist LV, Nagrath S, Ulkus L, Brannigan B, Collura CV, Inserra E, Diederichs S, Iafrate AJ, Bell DW, Digumarthy S, Muzikansky A, Irimia D, Settleman J, Tompkins RG, Lynch TJ, Toner M, Haber DA

Abstract

The use of tyrosine kinase inhibitors to target the epidermal growth factor receptor gene (EGFR) in patients with non-small-cell lung cancer is effective but limited by the emergence of drug-resistance mutations. Molecular characterization of circulating tumor cells may provide a strategy for noninvasive serial monitoring of tumor genotypes during treatment. We captured highly purified circulating tumor cells from the blood of patients with non-small-cell lung cancer using a microfluidic device containing microposts coated with antibodies against epithelial cells. We performed EGFR mutational analysis on DNA recovered from circulating tumor cells using allele-specific polymerase-chain-reaction amplification and compared the results with those from concurrently isolated free plasma DNA and from the original tumor-biopsy specimens. We isolated circulating tumor cells from 27 patients with metastatic non-small-cell lung cancer (median number, 74 cells per milliliter). We identified the expected EGFR activating mutation in circulating tumor cells from 11 of 12 patients (92%) and in matched free plasma DNA from 4 of 12 patients (33%) (P=0.009). We detected the T790M mutation, which confers drug resistance, in circulating tumor cells collected from patients with EGFR mutations who had received tyrosine kinase inhibitors. When T790M was detectable in pretreatment tumor-biopsy specimens, the presence of the mutation correlated with reduced progression-free survival (7.7 months vs. 16.5 months, P<0.001). Serial analysis of circulating tumor cells showed that a reduction in the number of captured cells was associated with a radiographic tumor response; an increase in the number of cells was associated with tumor progression, with the emergence of additional EGFR mutations in some cases. Molecular analysis of circulating tumor cells from the blood of patients with lung cancer offers the possibility of monitoring changes in epithelial tumor genotypes during the course of treatment.

MeSH Terms
Adult Aged Carcinoma, Non-Small-Cell Lung/drug therapy,genetics,pathology DNA Mutational Analysis/methods DNA, Neoplasm/analysis Disease Progression Drug Monitoring/methods Female Genes, erbB-1 Genetic Markers Genotype Humans Kaplan-Meier Estimate Lung Neoplasms/drug therapy,genetics,pathology Male Microfluidic Analytical Techniques Middle Aged Mutation Neoplastic Cells, Circulating Nucleic Acid Amplification Techniques Proportional Hazards Models Protein Kinase Inhibitors/therapeutic use
Chemicals
DNA, Neoplasm Genetic Markers Protein Kinase Inhibitors
Authors & Affiliations
18 authors, click to expand affiliations / ORCID
Maheswaran Shyamala
Massachusetts General Hospital Cancer Center, Boston 02129, USA.
Sequist Lecia V
Nagrath Sunitha
Ulkus Lindsey
Brannigan Brian
Collura Chey V
Inserra Elizabeth
Diederichs Sven
Iafrate A John
Bell Daphne W
Digumarthy Subba
Muzikansky Alona
Irimia Daniel
Settleman Jeffrey
Tompkins Ronald G
Lynch Thomas J
Toner Mehmet
Haber Daniel A
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Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
1533-4406
Published
2008-07-24
Epub
2008-00-02
Pages
366-77
Language
English
Region
United States
NLM ID
0255562
PMCID
PMC3551471
Subset
IM
Grants
Howard Hughes Medical Institute · United States
NIBIB NIH HHS · P41 EB002503 · United States
NCI NIH HHS · R01 CA129933 · United States
NCI NIH HHS · R01 CA129933-01A1 · United States
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