4.4 Article

Symptom and Quality of Life Improvement in LUX-Lung 8, an Open-Label Phase III Study of Second-Line Afatinib Versus Erlotinib in Patients With Advanced Squamous Cell Carcinoma of the Lung After First-Line Platinum-Based Chemotherapy

Journal

CLINICAL LUNG CANCER
Volume 19, Issue 1, Pages 74-+

Publisher

CIG MEDIA GROUP, LP
DOI: 10.1016/j.cllc.2017.06.002

Keywords

Cough; Diarrhea; Dyspnea; EGFR; Pain

Categories

Funding

  1. National Health Service at The Royal Marsden
  2. Boehringer Ingelheim
  3. Helen Wilkinson and Helen Kitchen of GeoMed
  4. Ashfield company, part of UDG Healthcare plc
  5. Institute of Cancer Research

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The effect of treatment on health-related quality of life (HRQoL) is an important consideration for patients. In the LUX-Lung 8 trial, second-line afatinib improved survival outcomes versus erlotinib in patients with squamous cell carcinoma of the lung. In this report, afatinib was also associated with improvements in disease-related symptoms and HRQoL versus erlotinib, contributing to the overall clinical benefit of afatinib. Introduction: In the phase III LUX-Lung 8 trial, afatinib significantly improved progression-free survival (PFS) and overall survival (OS) versus erlotinib in patients with squamous cell carcinoma (SCC) of the lung progressing during or after platinum-based chemotherapy. Patient-reported outcomes (PROs) and health-related quality of life (QoL) in these patients are presented. Patients and Methods: Patients (n = 795) were randomized 1: 1 to oral afatinib (40 mg/d) or erlotinib (150 mg/d). PROs were collected (baseline, every 28 days until progression, 28 days after discontinuation) using the European Organization for Research and Treatment of Cancer QoL questionnaire and lung cancer-specific module. The percentage of patients improved during therapy, time to deterioration (TTD), and changes over time were analyzed for prespecified lung cancer-related symptoms and global health status (GHS)/QoL. Results: Questionnaire compliance was 77.3% to 99.0% and 68.7% to 99.0% with afatinib and erlotinib, respectively. Significantly more patients who received afatinib versus erlotinib experienced improved scores for GHS/QoL (36% vs. 28%; P = .041) and cough (43% vs. 35%; P = .029). Afatinib significantly delayed TTD in dyspnea (P = .008) versus erlotinib, but not cough (P = .256) or pain (P = .869). Changes in mean scores favored afatinib for cough (P = .0022), dyspnea (P = .0007), pain (P = .0224), GHS/QoL (P = .0320), and all functional scales. Differences in adverse events between afatinib and erlotinib, specifically diarrhea, did not affect GHS/QoL. Conclusion: In patients with SCC of the lung, second-line afatinib was associated with improved prespecified disease-related symptoms and GHS/QoL versus erlotinib, complementing PFS and OS benefits with afatinib. (C) 2017 The Authors. Published by Elsevier Inc.

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