Science and Research

Nivolumab plus ipilimumab versus chemotherapy as first-line treatment in advanced non-small-cell lung cancer with high tumour mutational burden: patient-reported outcomes results from the randomised, open-label, phase III CheckMate 227 trial

BACKGROUND: In the phase III CheckMate 227 study, first-line nivolumab + ipilimumab significantly prolonged progression-free survival (co-primary end-point) versus chemotherapy in patients with advanced non-small-cell lung cancer (NSCLC) and high tumour mutational burden (TMB; >/=10 mutations/megabase). AIM: To evaluate patient-reported outcomes (PROs) in this population. METHODS: Disease-related symptoms and general health status were assessed using the validated PRO questionnaires Lung Cancer Symptom Scale (LCSS) and EQ-5D, respectively. LCSS average symptom burden index (ASBI) and three-item global index (3-IGI) and EQ-5D visual analogue scale (VAS) and utility index (UI) scores and changes from baseline were analysed descriptively. Longitudinal changes were assessed by mixed-effect model repeated measures (MMRMs) and time to first deterioration/improvement analyses. RESULTS: In the high TMB population, PRO questionnaire completion rates were approximately 90% at baseline and >80% for most on-treatment assessments. During treatment, mean changes from baseline with nivolumab + ipilimumab showed early, clinically meaningful improvements in LCSS ASBI/3-IGI and EQ-5D VAS/UI; with chemotherapy, symptoms and health-related quality of life remained stable (LCSS ASBI/3-IGI, EQ-5D UI) or improved following induction (EQ-5D VAS). MMRM-assessed changes in symptom burden were improved with nivolumab + ipilimumab versus chemotherapy. Symptom deterioration by week 12 was lower with nivolumab + ipilimumab versus chemotherapy (22.3% versus 35.0%; absolute risk reduction: 12.7% [95% confidence interval 2.4-22.5]), irrespective of discontinuation. Time to first deterioration was delayed with nivolumab + ipilimumab versus chemotherapy across LCSS and EQ-5D summary measures. CONCLUSION: First-line nivolumab + ipilimumab demonstrated early, sustained improvements in PROs versus chemotherapy in patients with advanced NSCLC and high TMB. CLINICAL TRIAL REGISTRATION: NCT02477826.

  • Reck, M.
  • Schenker, M.
  • Lee, K. H.
  • Provencio, M.
  • Nishio, M.
  • Lesniewski-Kmak, K.
  • Sangha, R.
  • Ahmed, S.
  • Raimbourg, J.
  • Feeney, K.
  • Corre, R.
  • Franke, F. A.
  • Richardet, E.
  • Penrod, J. R.
  • Yuan, Y.
  • Nathan, F. E.
  • Bhagavatheeswaran, P.
  • DeRosa, M.
  • Taylor, F.
  • Lawrance, R.
  • Brahmer, J.

Keywords

  • Antineoplastic agents
  • Carcinoma
  • Ipilimumab
  • Lung neoplasms
  • Nivolumab
  • Non-small-cell lung cancer
  • Platinum-doublet chemotherapy
  • Quality of life
  • Surveys and questionnaires
Publication details
DOI: 10.1016/j.ejca.2019.05.008
Journal: Eur J Cancer
Pages: 137-147 
Work Type: Original
Location: UGMLC
Disease Area: LC
Partner / Member: Ghd
Access-Number: 31195357
See publication on PubMed

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