EGFR tyrosine kinase inhibitors versus chemotherapy in EGFR wild-type pre-treated advanced nonsmall cell lung cancer in daily practice

Pascale Tomasini, Solenn Brosseau, Julien Mazières, Jean-Philippe Merlio, Michèle Beau-Faller, Jean Mosser, Marie Wislez, L'Houcine Ouafik, Benjamin Besse, Isabelle Rouquette, Didier Debieuvre, Fabienne Escande, Virginie Westeel, Clarisse Audigier-Valette, Pascale Missy, Alexandra Langlais, Frank Morin, Denis Moro-Sibilot, Gérard Zalcman, Fabrice Barlesi, Pascale Tomasini, Solenn Brosseau, Julien Mazières, Jean-Philippe Merlio, Michèle Beau-Faller, Jean Mosser, Marie Wislez, L'Houcine Ouafik, Benjamin Besse, Isabelle Rouquette, Didier Debieuvre, Fabienne Escande, Virginie Westeel, Clarisse Audigier-Valette, Pascale Missy, Alexandra Langlais, Frank Morin, Denis Moro-Sibilot, Gérard Zalcman, Fabrice Barlesi

Abstract

Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) are approved for second-line treatment of EGFR wild-type (EGFR-wt) nonsmall cell lung cancer (NSCLC). However, results from randomised trials performed to compare EGFR-TKIs with chemotherapy in this population did not show any survival benefit. In the era of immunotherapy, many drugs are approved for second-line treatment of EGFR-wt NSCLC and there is a need to reassess the role of EGFR-TKIs in this setting.The Biomarkers France study is a large nationwide cohort of NSCLC patients tested for EGFR mutations. We used this database to collect clinical, biological, treatment and outcome data on EGFR-wt patients who received second-line treatment with either EGFR-TKIs or chemotherapy.Among 1278 patients, 868 received chemotherapy and 410 received an EGFR-TKI. Median overall survival and progression-free survival were longer with chemotherapy than with an EGFR-TKI. Overall survival was 8.38 versus 4.99 months, respectively (hazard ratio 0.70, 95% CI 0.59-0.83; p<0.0001) and progression-free survival was 4.30 versus 2.83 months, respectively (hazard ratio 0.66, 95% CI 0.57-0.77; p<0.0001).This study is helpful to guide a multiline treatment strategy for EGFR-wt NSCLC patients. Immunotherapy is approved for second-line treatment. For third-line treatment, chemotherapy results in longer overall survival and progression-free survival, and should be preferred to EGFR-TKIs.

Trial registration: ClinicalTrials.gov NCT01700582.

Conflict of interest statement

Conflict of interest: Disclosures can be found alongside this article at erj.ersjournals.com

Copyright ©ERS 2017.

References

    1. N Engl J Med. 2015 Oct 22;373(17):1627-39
    1. J Clin Oncol. 2008 Sep 10;26(26):4244-52
    1. J Clin Oncol. 2013 Sep 20;31(27):3327-34
    1. Lancet Oncol. 2013 Sep;14 (10 ):981-8
    1. Lancet Oncol. 2014 Feb;15(2):143-55
    1. Lancet. 2014 Aug 23;384(9944):665-73
    1. J Clin Oncol. 2014 Jun 20;32(18):1902-8
    1. Lancet. 2008 Nov 22;372(9652):1809-18
    1. Clin Cancer Res. 2010 Feb 15;16(4):1307-14
    1. Lung Cancer. 2013 May;80(2):197-202
    1. Lancet Oncol. 2012 Mar;13(3):239-46
    1. J Thorac Oncol. 2016 Apr;11(4 Suppl):S115
    1. Ann Oncol. 2014 Dec;25(12):2385-91
    1. Lancet Oncol. 2016 Dec;17 (12 ):1661-1671
    1. Lancet Oncol. 2016 Mar;17(3):299-308
    1. Lancet Oncol. 2015 Aug;16(8):897-907
    1. Lancet. 2016 Apr 9;387(10027):1540-50
    1. Eur J Cancer. 2009 Jan;45(2):228-47
    1. Nature. 2008 Oct 23;455(7216):1069-75
    1. J Clin Oncol. 2008 Sep 10;26(26):4268-75
    1. Lancet Oncol. 2012 Mar;13(3):300-8
    1. J Clin Oncol. 2011 Oct 1;29(28):3825-31
    1. Lancet. 2005 Oct 29-Nov 4;366(9496):1527-37
    1. N Engl J Med. 2005 Jul 14;353(2):123-32
    1. N Engl J Med. 2015 Jul 9;373(2):123-35
    1. Cancer. 2013 Aug 1;119(15):2754-64
    1. Comput Methods Programs Biomed. 2004 Jul;75(1):45-9
    1. Lancet. 2016 Apr 2;387(10026):1415-1426
    1. N Engl J Med. 2009 Sep 3;361(10):947-57
    1. Lancet. 2016 Apr 30;387(10030):1837-46

Source: PubMed

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