Abstract

We read with great interest the article of Ma and colleagues titled “An exploratory comparative analysis of tyrosine kinase inhibitors or docetaxel in second-line treatment of EGFR wild-type non-small-cell lung cancer: a retrospective real-world practice review at a single tertiary care centre” [...]

Highlights

  • We read with great interest the article of Ma and colleagues titled “An exploratory comparative analysis of tyrosine kinase inhibitors or docetaxel in second-line treatment of EGFR wild-type non-small-cell lung cancer: a retrospective real-world practice review at a single tertiary care centre”[1]

  • The authors concluded that second-line therapy with tki for EGFR wild-type nsclc was associated with statistically better progression-free survival and event-free survival, and noninferior overall survival

  • Considering the results of two large randomized phase iii trials[2,3] and a meta-analysis[4], it is well established that chemotherapy is better than erlotinib in terms of pfs in the second-line treatment of nsclc with wild-type EGFR status

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Summary

Introduction

We read with great interest the article of Ma and colleagues titled “An exploratory comparative analysis of tyrosine kinase inhibitors or docetaxel in second-line treatment of EGFR wild-type non-small-cell lung cancer: a retrospective real-world practice review at a single tertiary care centre”[1]. The authors concluded that second-line therapy with tki for EGFR wild-type nsclc (compared with docetaxel) was associated with statistically better progression-free survival (pfs) and event-free survival, and noninferior overall survival. In addition to the limitations reported by the authors (the relatively small size of the cohort, the selection bias, the variability in the timing of imaging, and the retrospective nature of the analysis), we can make several comments.

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