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

نویسندگان

  • 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
چکیده

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.

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عنوان ژورنال:

دوره 50  شماره 

صفحات  -

تاریخ انتشار 2017