Value of KRAS as prognostic or predictive marker in NSCLC: Results from the TAILOR trial

E. Rulli, M. Marabese, V. Torri, G. Farina, S. Veronese, A. Bettini, F. Longo, L. Moscetti, M. Ganzinelli, C. Lauricella, E. Copreni, R. Labianca, O. Martelli, S. Marsoni, Massimo Broggini, M. C. Garassino

Research output: Contribution to journalArticlepeer-review


Background: The prognostic and predictive role of KRAS mutations in advanced nonsmall-cell lung cancer (NSCLC) is still unclear. TAILOR prospectively assessed the prognostic and predictive value of KRAS mutations in NSCLC patients treated with erlotinib or docetaxel in second line. Patients and methods: NSCLC patients from 52 Italian hospitals were genotyped for KRAS and EGFR mutational status in two independent laboratories. Wild-type EGFR patients (N = 218) received first-line platinum-based chemotherapy and were randomly allocated at progression to erlotinib or docetaxel. Overall survival (OS) according to KRAS mutational status was the primary end point. Results: KRAS mutations were present in 23% of TAILOR randomized cases. The presence of a KRAS mutation did not adversely affect progression-free (PFS) or overall (OS) survival [hazard ratio (HR) PFS = 1.01, 95% confidence interval (CI) 0.71-1.41, P = 0.977; OS = 1.24, 95% CI 0.87-1.77, P = 0.233], nor influenced treatment outcome (test for interaction: OS P = 0.965; PFS P = 0.417). Patients randomized to docetaxel treatment experienced longer survival independently from the KRAS mutational status of their tumors (HR: mutated KRAS 0.81, 95% CI 0.45-1.47; wild-type KRAS 0.79, 95% CI 0.57-1.10). Conclusion: In TAILOR, KRAS was neither prognostic nor predictive of benefit for either docetaxel or erlotinib. Docetaxel remains superior independently from KRAS status for second-line treatment in EGFR wild-type advanced NSCLC patients.

Original languageEnglish
Article numbermdv318
Pages (from-to)2079-2084
Number of pages6
JournalAnnals of Oncology
Issue number10
Publication statusPublished - Oct 1 2015


  • Docetaxel
  • Erlotinib
  • KRAS

ASJC Scopus subject areas

  • Oncology
  • Hematology


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