Impact of epidermal growth factor receptor gene expression level on clinical outcomes in epidermal growth factor receptor mutant lung adenocarcinoma patients taking first-line epidermal growth factor receptor–tyrosine kinase inhibitors. Issue 3 (March 2017)
- Record Type:
- Journal Article
- Title:
- Impact of epidermal growth factor receptor gene expression level on clinical outcomes in epidermal growth factor receptor mutant lung adenocarcinoma patients taking first-line epidermal growth factor receptor–tyrosine kinase inhibitors. Issue 3 (March 2017)
- Main Title:
- Impact of epidermal growth factor receptor gene expression level on clinical outcomes in epidermal growth factor receptor mutant lung adenocarcinoma patients taking first-line epidermal growth factor receptor–tyrosine kinase inhibitors
- Authors:
- Chang, Huang-Chih
Chen, Yu-Mu
Tseng, Chia-Cheng
Huang, Kuo-Tung
Wang, Chin-Chou
Chen, Yung-Che
Lai, Chien-Hao
Fang, Wen-Feng
Kao, Hsu-Ching
Lin, Meng-Chih - Abstract:
- Epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) are first-choice treatments for advanced non-small-cell lung cancer patients harboring EGFR mutations. Although EGFR mutations are strongly predictive of patients' outcomes and their response to treatment with EGFR-TKIs, early failure of first-line therapy with EGFR-TKIs in patients with EGFR mutations is not rare. Besides several clinical factors influencing EGFR-TKI efficacies studied earlier such as the Eastern Cooperative Oncology Group performance status or uncommon mutation, we would like to see whether semi-quantify EGFR mutation gene expression calculated by 2 −ΔΔct was a prognostic factor in EGFR-mutant non-small cell lung cancer patients receiving first-line EGFR-TKIs. This retrospective study reviews 926 lung cancer patients diagnosed from January 2011 to October 2013 at the Kaohsiung Chang Gung Memorial Hospital in Taiwan. Of 224 EGFR-mutant adenocarcinoma patients, 148 patients who had 2 −ΔΔct data were included. The best cutoff values of 2 −ΔΔct for in-frame deletions in exon 19 (19 deletion) and a position 858 substituted from leucine (L) to an arginine (R) in exon 21 (L858R) were determined using receiver operating characteristic curves. Patients were divided into high and low 2 −ΔΔct expression based on the above cutoff level. The best cutoff point of 2 −ΔΔct value of 19 deletion and L858R was 31.1 and 104.7, respectively. In all, 92 (62.1%) patients showed high 2 −ΔΔct expression andEpidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) are first-choice treatments for advanced non-small-cell lung cancer patients harboring EGFR mutations. Although EGFR mutations are strongly predictive of patients' outcomes and their response to treatment with EGFR-TKIs, early failure of first-line therapy with EGFR-TKIs in patients with EGFR mutations is not rare. Besides several clinical factors influencing EGFR-TKI efficacies studied earlier such as the Eastern Cooperative Oncology Group performance status or uncommon mutation, we would like to see whether semi-quantify EGFR mutation gene expression calculated by 2 −ΔΔct was a prognostic factor in EGFR-mutant non-small cell lung cancer patients receiving first-line EGFR-TKIs. This retrospective study reviews 926 lung cancer patients diagnosed from January 2011 to October 2013 at the Kaohsiung Chang Gung Memorial Hospital in Taiwan. Of 224 EGFR-mutant adenocarcinoma patients, 148 patients who had 2 −ΔΔct data were included. The best cutoff values of 2 −ΔΔct for in-frame deletions in exon 19 (19 deletion) and a position 858 substituted from leucine (L) to an arginine (R) in exon 21 (L858R) were determined using receiver operating characteristic curves. Patients were divided into high and low 2 −ΔΔct expression based on the above cutoff level. The best cutoff point of 2 −ΔΔct value of 19 deletion and L858R was 31.1 and 104.7, respectively. In all, 92 (62.1%) patients showed high 2 −ΔΔct expression and 56 patients (37.9%) low 2 −ΔΔct expression. The mean age was 65.6 years. Progression-free survival of 19 deletion mutant patients with low versus high expression level was 17.07 versus 12.04 months (P = 0.004), respectively. Progression-free survival of L858 mutant patients was 13.75 and 7.96 months (P = 0.008), respectively. EGFR-mutant lung adenocarcinoma patients with lower EGFR gene expression had longer progression-free survival duration without interfering overall survival. … (more)
- Is Part Of:
- Tumor biology. Volume 39:Issue 3(2017)
- Journal:
- Tumor biology
- Issue:
- Volume 39:Issue 3(2017)
- Issue Display:
- Volume 39, Issue 3 (2017)
- Year:
- 2017
- Volume:
- 39
- Issue:
- 3
- Issue Sort Value:
- 2017-0039-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2017-03
- Subjects:
- Lung cancer adenocarcinoma -- EGFR mutation -- tyrosine kinase inhibitors -- polymerase chain reaction (PCR) -- oncogene
Cancer -- Periodicals
Oncology -- Periodicals
Tumors -- Periodicals
616.994 - Journal URLs:
- https://www.iospress.nl/journal/tumor-biology/ ↗
https://uk.sagepub.com/en-gb/eur/tumor-biology/journal202707 ↗
http://www.springer.com/gb/ ↗ - DOI:
- 10.1177/1010428317695939 ↗
- Languages:
- English
- ISSNs:
- 1010-4283
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9070.645500
British Library DSC - BLDSS-3PM
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- 7612.xml