Literature DB >> 27393514

Advanced non-Small cell lung cancer patients at the extremes of age in the era of epidermal growth factor receptor tyrosine kinase inhibitors.

Yu-Mu Chen1, Chien-Hao Lai2, Kun-Ming Rau3, Cheng-Hua Huang4, Huang-Chih Chang5, Tung-Ying Chao6, Chia-Cheng Tseng7, Wen-Feng Fang8, Yung-Che Chen9, Yu-Hsiu Chung10, Yi-Hsi Wang11, Mao-Chang Su12, Kuo-Tung Huang13, Shih-Feng Liu14, Hung-Chen Chen15, Ya-Chun Chang16, Yu-Ping Chang17, Chin-Chou Wang18, Meng-Chih Lin19.   

Abstract

OBJECTIVES: The clinical characteristics and survival of very young (≤40 years) and very old (>80years) patients with advanced non-small cell lung cancer (NSCLC) are distinct. However, the benefits of epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) to patients at the extremes of age with NSCLC harboring EGFR mutation have not been well studied. We retrospectively studied the effect of extreme age on patients' clinical characteristics and prognosis.
MATERIALS AND METHODS: Of 1510 lung cancer patients diagnosed between November 2010 and March 2014, 555 patients who were tested for EGFR mutations were included. Patients were divided into the following groups according to age: young (≤40 years), lower medium (41-60 years), higher medium (61-80years), and very old (>80years).
RESULTS: Of the 555 patients, 20 (3.6%) patients were aged ≤40 years and 60 (10.8%) patients were aged >80years. Young NSCLC patients had a lower BMI (p=0.003), more brain (p=0.016) and bone metastases (p=0.002) Very young lung cancer patients still have poor prognosis even they were EGFR mutant. (EGFR mutant vs. wild type patients, OS: 12 vs. 7.3 months, p=0.215) Very old NSCLC patients had a lower BMI (p=0.003) and poor ECOG PS (p=0.028). Positive EGFR mutation test reverses poor prognosis of elderly NSCLC patients. (EGFR mutant vs. wild type patients, OS: 13.2 vs. 4.9 months, p=0.003)
CONCLUSION: We observed EGFR mutations reverse the poor prognosis of old patients with NSCLC. However, young patients with lung cancer have a poor prognosis even if they harbor EGFR mutations.
Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Elderly lung cancer; Extreme age; Non-small cell lung cancer; Tyrosine kinase inhibitor; Young lung cancer

Mesh:

Substances:

Year:  2016        PMID: 27393514     DOI: 10.1016/j.lungcan.2016.05.020

Source DB:  PubMed          Journal:  Lung Cancer        ISSN: 0169-5002            Impact factor:   5.705


  8 in total

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Journal:  Invest New Drugs       Date:  2016-10-29       Impact factor: 3.850

3.  Frequent genomic alterations and better prognosis among young patients with non-small-cell lung cancer aged 40 years or younger.

Authors:  X Pan; T Lv; F Zhang; H Fan; H Liu; Y Song
Journal:  Clin Transl Oncol       Date:  2018-02-19       Impact factor: 3.405

4.  Increased interleukin-17A-producing γδT cells predict favorable survival in elderly patients with LUAD and LUSC.

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5.  The impact of de novo liver metastasis on clinical outcome in patients with advanced non-small-cell lung cancer.

Authors:  Yu-Ping Chang; Yu-Mu Chen; Chien-Hao Lai; Chiung-Yu Lin; Wen-Feng Fang; Cherng-Hua Huang; Shau-Hsuan Li; Hung-Chen Chen; Chin-Chou Wang; Meng-Chih Lin
Journal:  PLoS One       Date:  2017-06-07       Impact factor: 3.240

6.  Computer-Aided Nodule Assessment and Risk Yield (CANARY) may facilitate non-invasive prediction of EGFR mutation status in lung adenocarcinomas.

Authors:  Ryan Clay; Benjamin R Kipp; Sarah Jenkins; Ron A Karwoski; Fabien Maldonado; Srinivasan Rajagopalan; Jesse S Voss; Brian J Bartholmai; Marie Christine Aubry; Tobias Peikert
Journal:  Sci Rep       Date:  2017-12-15       Impact factor: 4.379

7.  Intrinsically altered lung-resident γδT cells control lung melanoma by producing interleukin-17A in the elderly.

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Journal:  Aging Cell       Date:  2020-01-05       Impact factor: 9.304

8.  Active Treatment Improves Overall Survival in Extremely Older Non-Small Cell Lung Cancer Patients: A Multicenter Retrospective Cohort Study.

Authors:  Su Yeon Lee; Yoon-Ki Hong; Wonjun Ji; Jae Cheol Lee; Chang Min Choi
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  8 in total

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