Literature DB >> 27229180

The International Association for the Study of Lung Cancer Consensus Statement on Optimizing Management of EGFR Mutation-Positive Non-Small Cell Lung Cancer: Status in 2016.

Daniel S W Tan1, Sue S Yom2, Ming S Tsao3, Harvey I Pass4, Karen Kelly5, Nir Peled6, Rex C Yung7, Ignacio I Wistuba8, Yasushi Yatabe9, Michael Unger10, Philip C Mack5, Murry W Wynes11, Tetsuya Mitsudomi12, Walter Weder13, David Yankelevitz14, Roy S Herbst15, David R Gandara5, David P Carbone16, Paul A Bunn17, Tony S K Mok18, Fred R Hirsch17.   

Abstract

Mutations in the epidermal growth factor receptor gene (EGFR) represent one of the most frequent "actionable" alterations in non-small cell lung cancer (NSCLC). Typified by high response rates to targeted therapies, EGFR tyrosine kinase inhibitors (TKIs) are now established first-line treatment options and have transformed the treatment paradigm for NSCLC. With the recent breakthrough designation and approval of the third-generation EGFR TKI osimertinib, available systemic and local treatment options have expanded, requiring new clinical algorithms that take into account individual patient molecular and clinical profiles. In this International Association for the Study of Lung Cancer commissioned consensus statement, key pathologic, diagnostic, and therapeutic considerations, such as optimal choice of EGFR TKI and management of brain metastasis, are discussed. In addition, recommendations are made for clinical guidelines and research priorities, such as the role of repeat biopsies and use of circulating free DNA for molecular studies. With the rapid pace of progress in treating EGFR-mutant NSCLC, this statement provides a state-of-the-art review of the contemporary issues in managing this unique subgroup of patients.
Copyright © 2016 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Brain metastases; EGFR mutation; Non–small cell lung cancer; Resistance; Therapy; Tyrosine kinase inhibitor

Mesh:

Substances:

Year:  2016        PMID: 27229180     DOI: 10.1016/j.jtho.2016.05.008

Source DB:  PubMed          Journal:  J Thorac Oncol        ISSN: 1556-0864            Impact factor:   15.609


  69 in total

1.  Continued EGFR-TKI with concurrent radiotherapy to improve time to progression (TTP) in patients with locally progressive non-small cell lung cancer (NSCLC) after front-line EGFR-TKI treatment.

Authors:  Y Wang; Y Li; L Xia; K Niu; X Chen; D Lu; R Kong; Z Chen; J Sun
Journal:  Clin Transl Oncol       Date:  2017-08-03       Impact factor: 3.405

2.  Quality Assessment of Reporting Performance for EGFR Molecular Diagnosis in Non-Small Cell Lung Cancer.

Authors:  Yanxi Han; Rui Zhang; Guigao Lin; Kuo Zhang; Jiehong Xie; Jinming Li
Journal:  Oncologist       Date:  2017-07-12

3.  Liquid biopsy in the practice of neo-oncology.

Authors:  Smadar Geva; Laila C Roisman; Nir Peled
Journal:  J Thorac Dis       Date:  2016-10       Impact factor: 2.895

Review 4.  Liquid biopsy based biomarkers in non-small cell lung cancer for diagnosis and treatment monitoring.

Authors:  David Pérez-Callejo; Atocha Romero; Mariano Provencio; María Torrente
Journal:  Transl Lung Cancer Res       Date:  2016-10

5.  Combination of stereotactic radiotherapy and targeted therapy: patterns-of-care survey in German-speaking countries.

Authors:  S G C Kroeze; C Fritz; L Basler; E Gkika; T B Brunner; A L Grosu; M Guckenberger
Journal:  Strahlenther Onkol       Date:  2019-02-08       Impact factor: 3.621

6.  Targeting the metastatic niche through anti-angiogenic approaches in epidermal growth factor receptor mutant non-small cell lung cancer.

Authors:  Wan Ling Tan; Daniel S W Tan
Journal:  Transl Lung Cancer Res       Date:  2018-02

Review 7.  Clinical management of epidermal growth factor receptor mutation-positive non-small cell lung cancer patients after progression on previous epidermal growth factor receptor tyrosine kinase inhibitors: the necessity of repeated molecular analysis.

Authors:  José Luís González-Larriba; Martín Lázaro-Quintela; Manuel Cobo; Manuel Dómine; Margarita Majem; Rosario García-Campelo
Journal:  Transl Lung Cancer Res       Date:  2017-12

8.  Increased miR-21a provides metabolic advantages through suppression of FBP1 expression in non-small cell lung cancer cells.

Authors:  Qingchun Dai; Na Li; Xiaohong Zhou
Journal:  Am J Cancer Res       Date:  2017-11-01       Impact factor: 6.166

9.  Method for preservation of DNA stability of liquid-based cytology specimens from a lung adenocarcinoma cell line.

Authors:  Yukiko Matsuo; Kazuya Yamashita; Tsutomu Yoshida; Yukitoshi Satoh
Journal:  Virchows Arch       Date:  2020-08-31       Impact factor: 4.064

10.  The value of AGR2 and KRT5 as an immunomarker combination in distinguishing lung squamous cell carcinoma from adenocarcinoma.

Authors:  Bo Pan; Zi-Xin Wei; Ju-Xuan Zhang; Xin Li; Qing-Wei Meng; Ying-Yue Cao; Li-Shuang Qi; Yan Yu
Journal:  Am J Transl Res       Date:  2021-05-15       Impact factor: 4.060

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