Science and Research

Nintedanib plus docetaxel as second-line therapy in patients with non-small-cell lung cancer of adenocarcinoma histology: a network meta-analysis vs new therapeutic options

PATIENTS & METHODS: We provide an update to a network meta-analysis evaluating the relative efficacy of nintedanib + docetaxel versus other second-line agents in adenocarcinoma histology non-small-cell lung cancer. RESULTS: Overall similarity of nintedanib + docetaxel versus ramucirumab + docetaxel, and versus nivolumab. Comparing nintedanib + docetaxel with nivolumab, hazards ratio (HR) of overall survival and progression-free survival (PFS) pointed in opposite directions (overall survival: HR: 1.20 [95% credible interval: 0.92-1.58]; PFS: HR: 0.91 [0.68-1.21]). Exploratory subgroup analysis indicated superiority of nivolumab in high PD-L1 expression level subgroups; results were more favorable for nintedanib in all subgroups with low (<1%, <5%, <10%) PD-L1 expression levels - in particular, with regard to PFS. CONCLUSION: Results demonstrated similar efficacy of nintedanib + docetaxel compared with the new therapeutic options ramucirumab + docetaxel and nivolumab, with potential differences in subgroups according to PD-L1 expression level.
  • Popat, S.
  • Mellemgaard, A.
  • Reck, M.
  • Hastedt, C.
  • Griebsch, I.

Keywords

  • Adenocarcinoma/*drug therapy/pathology
  • Antibodies, Monoclonal/therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols/administration & dosage
  • B7-H1 Antigen/genetics
  • Carcinoma, Non-Small-Cell Lung/*drug therapy/pathology
  • Disease-Free Survival
  • Gene Expression Regulation, Neoplastic/drug effects
  • Humans
  • Indoles/adverse effects/*therapeutic use
  • Network Meta-Analysis
  • Taxoids/adverse effects/*therapeutic use
  • Treatment Outcome
  • Nsclc
  • chemotherapy
  • immunotherapy
  • nintedanib
  • nivolumab
  • second-line treatment
Publication details
DOI: 10.2217/fon-2016-0493
Journal: Future oncology (London, England)
Pages: 1159-1171 
Number: 13
Work Type: Original
Location: ARCN
Disease Area: LC
Partner / Member: Ghd
Access-Number: 28326832
See publication on PubMed

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