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Overall Survival Analysis and Characterization of an EGFR Mutated Non-Small Cell Lung Cancer (NSCLC) Population
被引:2
|作者:
Aguiar, Filipa
[1
]
Fernandes, Gabriela
[2
,3
]
Queiroga, Henrique
[2
,3
]
Machado, Jose Carlos
[3
,4
,5
]
Cirnes, Luis
[4
,5
]
Moura, Conceicao Souto
[6
]
Hespanhol, Venceslau
[2
,3
]
机构:
[1] Hosp Braga, Pneumol Dept, Braga, Portugal
[2] Ctr Hosp Sao Joao, Pneumol Dept, Oporto, Portugal
[3] Univ Porto, Fac Med, Oporto, Portugal
[4] Univ Porto, i3S Inst Invest & Inovacao Saude, Oporto, Portugal
[5] Univ Porto, Ipatimup Inst Mol Pathol & Immunol, Oporto, Portugal
[6] Ctr Hosp Sao Joao, Anat Pathol Dept, Oporto, Portugal
来源:
ARCHIVOS DE BRONCONEUMOLOGIA
|
2018年
/
54卷
/
01期
关键词:
Epidermal Growth Factor Receptor;
Tyrosine Kinase Inhibitors;
Lung cancer overall survival;
Non-Small Cell Lung Cancer;
Lung;
GROWTH-FACTOR RECEPTOR;
1ST-LINE TREATMENT;
OPEN-LABEL;
ASIAN PATIENTS;
MUTATIONS;
GEFITINIB;
CHEMOTHERAPY;
MULTICENTER;
ERLOTINIB;
PLUS;
D O I:
暂无
中图分类号:
R56 [呼吸系及胸部疾病];
学科分类号:
摘要:
Background: Patients with activating somatic mutations in the Epidermal Growth Factor Receptor (EGFR) have better clinical outcomes when treated with Tyrosine Kinase Inhibitors (TKI) over chemotherapy. However, the impact of the use of TKIs on overall survival outside clinical trials is not well established. Objective: To characterize and analyze the overall survival of a Caucasian population with NSCLC and EGFR mutations. Methods: A retrospective cohort analysis of patients with NSCLC screened for EGFR mutations (exons 18-21) between October 2009 and July 2013 was conducted. Clinical and pathological characteristics, mutational EGFR status, treatment and overall survival were evaluated. Results: From the 285 patients which performed screening for EGFR mutations, 54 (18.9%) had mutations, 25 (46.3%) of which in exon 19 and 20 of which (37.0%) in exon 21. The occurrence of mutations was associated with female sex and non-smoking habits (both, P<.001). The median survival of the global population was 12.0 months, with a better overall survival in mutated than non-mutated patients (20.0 vs 11.0 months, respectively; P = .007). Conclusion: These data contribute for a better knowledge of our lung cancer population concerning the mutational status and clinical outcomes, confirming a better overall survival for the patients with EGFR TKI sensible mutations. (C) 2017 SEPAR. Published by Elsevier Espana, S.L.U. All rights reserved.
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页码:10 / 17
页数:8
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