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Monitoring efficacy of checkpoint inhibitor therapy in patients with non-small-cell lung cancer.

Abstract
Aim: Radiological criteria alone do not reflect the entire population benefitting from checkpoint inhibitor therapy (CIT). This study aimed to detect patterns to assess CIT efficacy in non-small-cell lung cancer (NSCLC) patients. Materials & methods: We evaluated clinical, radiological and laboratory parameters in a retrospective cohort of NSCLC patients treated with nivolumab. Results: A total of 51 patients were included in the analysis. Most single parameters failed to reflect treatment benefit. Three laboratory parameters (lactate dehydrogenase, C-reactive protein and the neutrophil/lymphocyte ratio) combined in a weighted score could predict benefit with a sensitivity of 92.3% and a hazard ratio of 0.31 (95% CI: 0.16-0.59) in an early phase of therapy. Sorting patients by score showed a 1-year survival of 36% in those predicted as not benefitting versus 68% in those predicted to benefit. Conclusion: A weighted score integrating common serum markers could help detect patients benefitting from checkpoint inhibitors during ongoing CIT.
AuthorsAnnett Schiwitza, Hans-Ulrich Schildhaus, Birgit Zwerger, Josef Rüschoff, Christian Reinhardt, Andreas Leha, Stefan Andreas, Achim Rittmeyer
JournalImmunotherapy (Immunotherapy) Vol. 11 Issue 9 Pg. 769-782 (06 2019) ISSN: 1750-7448 [Electronic] England
PMID31120392 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents, Immunological
  • B7-H1 Antigen
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • Nivolumab
  • C-Reactive Protein
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Agents, Immunological (adverse effects, therapeutic use)
  • B7-H1 Antigen (antagonists & inhibitors, metabolism)
  • C-Reactive Protein (analysis)
  • Carcinoma, Non-Small-Cell Lung (drug therapy, metabolism, pathology)
  • Female
  • Humans
  • Lung Neoplasms (drug therapy, metabolism, pathology)
  • Male
  • Middle Aged
  • Nivolumab (adverse effects, therapeutic use)
  • Pneumonia (chemically induced)
  • Programmed Cell Death 1 Receptor (antagonists & inhibitors, metabolism)
  • Retrospective Studies
  • Survival Analysis
  • Treatment Outcome

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