Literature DB >> 24486058

Treatment of advanced non-small-cell lung cancer with epidermal growth factor receptor (EGFR) mutation or ALK gene rearrangement: results of an international expert panel meeting of the Italian Association of Thoracic Oncology.

Cesare Gridelli1, Filippo de Marinis2, Federico Cappuzzo3, Massimo Di Maio4, Fred R Hirsch5, Tony Mok6, Floriana Morgillo7, Rafael Rosell8, David R Spigel9, James Chih-Hsin Yang10, Fortunato Ciardiello7.   

Abstract

The availability of targeted drugs has made the assessment of the EGFR mutation and ALK rearrangement critical in choosing the optimal treatment for patients with advanced non-small-cell lung cancer (NSCLC). In May 2013, the Italian Association of Thoracic Oncology (AIOT) organized an International Experts Panel Meeting to review strengths and limitations of the available evidence for the diagnosis and treatment of advanced NSCLC with EGFR or anaplastic lymphoma kinase (ALK) alterations and to discuss implications for clinical practice and future clinical research. All patients with advanced NSCLC, with the exclusion of pure squamous cell carcinoma in former or current smokers, should be tested for EGFR mutations and ALK rearrangements before decisions are made on first-line treatment. First-line treatment of EGFR-mutated cases should be with an EGFR tyrosine kinase inhibitor (TKI). Any available agent (gefitinib, erlotinib, or afatinib) can be used, until further data from comparative studies may better guide TKI selection. As general rule, and when clinically feasible, results of EGFR mutational status should be awaited before starting first-line treatment. Panelists agreed that the use of crizotinib is justified in any line of treatment. Although solid evidence supporting the continuation of EGFR TKIs or crizotinib beyond progression is lacking, in some cases (minimal, asymptomatic progression, or oligoprogression manageable by local therapy), treatment continuation beyond progression could be justified. Experimental strategies to target tumor heterogeneity and to treat patients after failure of EGFR TKIs or crizotinib are considered high-priority areas of research. A number of relevant research priorities were identified to optimize available treatment options.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ALK rearrangement; Epidermal growth factor receptor mutation; Non–small-cell lung cancer

Mesh:

Substances:

Year:  2013        PMID: 24486058     DOI: 10.1016/j.cllc.2013.12.002

Source DB:  PubMed          Journal:  Clin Lung Cancer        ISSN: 1525-7304            Impact factor:   4.785


  25 in total

Review 1.  Molecular targeted therapy to improve radiotherapeutic outcomes for non-small cell lung carcinoma.

Authors:  Bhaskar Bhardwaj; Swaroop Revannasiddaiah; Himanshu Bhardwaj; Sree Balusu; Ali Shwaiki
Journal:  Ann Transl Med       Date:  2016-02

2.  Synergistic tumor suppression by a Perilla frutescens-derived methoxyflavanone and anti-cancer tyrosine kinase inhibitors in A549 human lung adenocarcinoma.

Authors:  Amer Ali Abd El-Hafeez; Takashi Fujimura; Rikiya Kamei; Noriko Hirakawa; Kenji Baba; Kazuhisa Ono; Seiji Kawamoto
Journal:  Cytotechnology       Date:  2017-07-29       Impact factor: 2.058

Review 3.  The Role of Thoracic Surgery in the Therapeutic Management of Metastatic Non-Small Cell Lung Cancer.

Authors:  Elizabeth A David; James M Clark; David T Cooke; Joy Melnikow; Karen Kelly; Robert J Canter
Journal:  J Thorac Oncol       Date:  2017-08-24       Impact factor: 15.609

4.  Stereotactic body radiotherapy for oligoprogressive cancer.

Authors:  Patrick Cheung
Journal:  Br J Radiol       Date:  2016-08-24       Impact factor: 3.039

Review 5.  Role of interim 18F-FDG-PET/CT for the early prediction of clinical outcomes of Non-Small Cell Lung Cancer (NSCLC) during radiotherapy or chemo-radiotherapy. A systematic review.

Authors:  Marta Cremonesi; Laura Gilardi; Mahila Esmeralda Ferrari; Gaia Piperno; Laura Lavinia Travaini; Robert Timmerman; Francesca Botta; Guido Baroni; Chiara Maria Grana; Sara Ronchi; Delia Ciardo; Barbara Alicja Jereczek-Fossa; Cristina Garibaldi; Roberto Orecchia
Journal:  Eur J Nucl Med Mol Imaging       Date:  2017-07-05       Impact factor: 9.236

6.  Cost Effectiveness of Alectinib vs. Crizotinib in First-Line Anaplastic Lymphoma Kinase-Positive Advanced Non-Small-Cell Lung Cancer.

Authors:  Josh J Carlson; Kangho Suh; Panos Orfanos; William Wong
Journal:  Pharmacoeconomics       Date:  2018-04       Impact factor: 4.981

7.  Non-Small-Cell Lung Cancer (NSCLC) Harboring ALK Translocations: Clinical Characteristics and Management in a Real-Life Setting: a French Retrospective Analysis (GFPC 02-14 Study).

Authors:  Jean-Bernard Auliac; Isabelle Monnet; Catherine Dubos-Arvis; Anne Marie Chiappa; Nathalie Baize; Suzana Bota; Alain Vergnenegre; Helene Doubre; Chrystele Locher; Acya Bizieux; Gilles Robinet; Christos Chouaid
Journal:  Target Oncol       Date:  2017-12       Impact factor: 4.493

8.  Fasting potentiates the anticancer activity of tyrosine kinase inhibitors by strengthening MAPK signaling inhibition.

Authors:  Irene Caffa; Vito D'Agostino; Patrizia Damonte; Debora Soncini; Michele Cea; Fiammetta Monacelli; Patrizio Odetti; Alberto Ballestrero; Alessandro Provenzani; Valter D Longo; Alessio Nencioni
Journal:  Oncotarget       Date:  2015-05-20

9.  Cost-Effectiveness of Lorlatinib as a First-Line Therapy for Untreated Advanced Anaplastic Lymphoma Kinase-Positive Non-Small Cell Lung Cancer.

Authors:  SiNi Li; JianHe Li; LiuBao Peng; YaMin Li; XiaoMin Wan
Journal:  Front Oncol       Date:  2021-05-28       Impact factor: 6.244

10.  Predictive value of STMN1 gene promoter polymorphism (-2166T>C) in patients with advanced NSCLC treated with the combination of platinum compounds and vinorelbine.

Authors:  Radosław Mlak; Paweł Krawczyk; Marzanna Ciesielka; Iwona Homa; Tomasz Powrózek; Monika Prendecka; Piotr Kozioł; Janusz Milanowski; Teresa Małecka-Massalska
Journal:  Cancer Chemother Pharmacol       Date:  2015-07-29       Impact factor: 3.333

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