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.
引用
收藏
页码:10 / 17
页数:8
相关论文
共 50 条
  • [21] The Plasma Concentration of Epidermal Growth Factor Receptor (EGFR) and Overall Survival (OS) in Non-Small Cell Lung Cancer (NSCLC) Patients
    Ye, P.
    Zhao, J.
    Maihle, N.
    Wang, S. L.
    Jin, J. Y.
    Kong, F. M. P.
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2015, 93 (03): : E445 - E445
  • [22] Molecular characteristics of HRAS mutated non-small cell lung cancer (NSCLC)
    Trabolsi, Asaad
    Rodriguez, Estelamari
    Kareff, Samuel Alexander
    Korn, Michael
    Xiu, Joanne
    Liu, Stephen
    Walker, Philip
    Ma, Patrick
    Mamdani, Hirva
    Nieva, Jorge
    Borghaei, Hossein
    Nabhan, Chadi
    Nagasaka, Misako
    Puri, Sonam
    Lopes, Gilberto
    [J]. CANCER RESEARCH, 2022, 82 (12)
  • [23] Overall survival analysis from the ADAURA trial of adjuvant osimertinib in patients with resected EGFR-mutated (EGFRm) stage IB-IIIA non-small cell lung cancer (NSCLC).
    Herbst, Roy S.
    Tsuboi, Masahiro
    John, Tom
    Kato, Terufumi
    Majem, Margarita
    Grohe, Christian
    Wang, Jie
    Goldman, Jonathan W.
    Lu, Shun
    Su, Wu-Chou
    de Marinis, Filippo
    Shepherd, Frances A.
    Lee, Ki Hyeong
    Le, Nhieu
    Dechaphunkul, Arunee
    Kowalski, Dariusz M.
    Poole, Lynne
    Stachowiak, Marta
    Rukazenkov, Yuri
    Wu, Yi-Long
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2023, 41 (17_SUPPL)
  • [24] Overall survival analysis from the ADAURA trial of adjuvant osimertinib in patients with resected EGFR-mutated (EGFRm) stage IB-IIIA non-small cell lung cancer (NSCLC).
    Herbst, Roy S.
    Tsuboi, Masahiro
    John, Tom
    Kato, Terufumi
    Majem, Margarita
    Grohe, Christian
    Wang, Jie
    Goldman, Jonathan W.
    Lu, Shun
    Su, Wu-Chou
    De Marinis, Filippo
    Shepherd, Frances A.
    Lee, Ki Hyeong
    Le, Nhieu
    Dechaphunkul, Arunee
    Kowalski, Dariusz M.
    Poole, Lynne
    Stachowiak, Marta
    Rukazenkov, Yuri
    Wu, Yi-Long
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2023, 41 (17)
  • [25] Treatment strategy of EGFR-mutated non-small cell lung cancer
    Tanaka, Fumihiro
    Yoneda, Kazue
    Takenaka, Masaru
    Kuroda, Koji
    [J]. JOURNAL OF THORACIC DISEASE, 2022, 14 (03) : 602 - 606
  • [26] Emerging drugs for EGFR-mutated non-small cell lung cancer
    Sukrithan, Vineeth
    Deng, Lei
    Barbar, Alexander
    Cheng, Haiying
    [J]. EXPERT OPINION ON EMERGING DRUGS, 2019, 24 (01) : 5 - 16
  • [27] How to Treat EGFR-Mutated Non-Small Cell Lung Cancer
    Belani, Neel
    Liang, Katherine
    Fradley, Michael
    Judd, Julia
    Borghaei, Hossein
    [J]. JACC: CARDIOONCOLOGY, 2023, 5 (04): : 542 - 545
  • [28] Safety of osimertinib in EGFR-mutated non-small cell lung cancer
    Mezquita, Laura
    Varga, Andreea
    Planchard, David
    [J]. EXPERT OPINION ON DRUG SAFETY, 2018, 17 (12) : 1239 - 1248
  • [29] Systemic treatment of EGFR-mutated non-small cell lung cancer
    Czyzykowski, Rafal L.
    Wrona, Ewa K.
    Talajko, Agata
    Hasinska, Aleksandra M.
    Potemski, Piotr J.
    [J]. ONCOLOGY IN CLINICAL PRACTICE, 2024,
  • [30] Relationship between age treatment and overall survival in patients with non-small cell lung cancer (NSCLC)
    Heras, P.
    Hatzopoulos, A.
    Kritikos, K.
    Georgopoulou, A.
    [J]. LUNG CANCER, 2007, 55 : S10 - S10