Abstract | BACKGROUND: MATERIALS AND METHODS: Serum samples were analyzed by Scorpion-ARMS to detect EGFR mutations before and after erlotinib administration. Agreement between serum and tumor EGFR mutations and time course changes of EGFR mutations were evaluated. RESULTS: A total of 95 of 103 patients consented to examination of serum samples; baseline serum EGFR mutations (exon 19 deletions or L858R) were detected in 25 patients (26.3%). The agreement rate between tumor and serum samples was 96.2%. Among 65 serum samples taken at 190 days after treatment initiation, EGFR mutations were detected in 5 patients (7.7%). Of the serum samples taken at progression (n = 71), EGFR mutations were detected in 16 patients (22.5%). Patients with baseline serum EGFR mutations had a median progression-free survival of 9.7 months; those without baseline serum mutations had a median progression-free survival of 15.2 months. CONCLUSION: The sensitivity of these analyses was not enough to draw firm conclusions; however, the results suggest that serum EGFR mutations correlate with disease activity.
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Authors | Makoto Nishio, Koichi Goto, Kenichi Chikamori, Toyoaki Hida, Nobuyuki Katakami, Makoto Maemondo, Norihisa Ohishi, Tomohide Tamura |
Journal | Clinical lung cancer
(Clin Lung Cancer)
Vol. 17
Issue 1
Pg. 24-9.e1
(Jan 2016)
ISSN: 1938-0690 [Electronic] United States |
PMID | 26336854
(Publication Type: Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved. |
Chemical References |
- Biomarkers, Tumor
- Protein Kinase Inhibitors
- Erlotinib Hydrochloride
- EGFR protein, human
- ErbB Receptors
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Biomarkers, Tumor
(blood, genetics)
- Carcinoma, Non-Small-Cell Lung
(blood, drug therapy, genetics, pathology)
- Disease Progression
- ErbB Receptors
(blood, genetics)
- Erlotinib Hydrochloride
(therapeutic use)
- Female
- Follow-Up Studies
- Genotype
- Humans
- Lung Neoplasms
(blood, drug therapy, genetics, pathology)
- Male
- Middle Aged
- Mutation
(genetics)
- Neoplasm Staging
- Polymerase Chain Reaction
- Prognosis
- Protein Kinase Inhibitors
(therapeutic use)
- Survival Rate
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