The association between tumor burden and severe immune-related adverse events in non-small cell lung cancer patients responding to immune-checkpoint inhibitor treatment

Lung Cancer. 2019 Apr:130:159-161. doi: 10.1016/j.lungcan.2019.02.011. Epub 2019 Feb 14.

Abstract

Objectives: The use of immune checkpoint inhibitors (ICIs) for advanced non-small cell lung cancer (NSCLC) has demonstrated survival benefits, although some treatment responders (defined as patients with non-progressive disease) are forced to discontinue treatment because of severe immune-related adverse events (irAEs). An association between treatment efficacy and irAEs has been reported. However, it is unclear which treatment responders are likely to develop severe irAEs. We aimed to examine risk factors for ICI-related severe irAEs in patients with NSCLC.

Materials and methods: Between February 2016 and October 2018, we retrospectively evaluated 42 patients with NSCLC at our institution who responded to ICI treatment. Tumor burden was measured as the sum of the unidimensional diameters of up to five target lesions, according to the Response Evaluation Criteria in Solid Tumors version 1.1.

Results: ICIs were discontinued in 15 of 42 treatment responders because of severe irAEs. Tumor burden was a significant independent predictor of severe irAEs (p = 0.03). The odds ratio of severe irAEs and tumor burden over 90 mm was 8.62 (95% confidence interval = 1.96-37.9, p = 0.004).

Conclusion: A high tumor burden was a risk factor for severe irAEs in patients with NSCLC who responded to ICI treatment.

Keywords: Immune checkpoint inhibitors; Immune-related adverse events; Non-small cell lung cancer; Tumor burden.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antibodies, Monoclonal / adverse effects
  • Antibodies, Monoclonal / pharmacology
  • Antibodies, Monoclonal / therapeutic use*
  • Carcinoma, Non-Small-Cell Lung / epidemiology
  • Carcinoma, Non-Small-Cell Lung / immunology
  • Carcinoma, Non-Small-Cell Lung / therapy*
  • Costimulatory and Inhibitory T-Cell Receptors / antagonists & inhibitors
  • Drug-Related Side Effects and Adverse Reactions / epidemiology*
  • Female
  • Humans
  • Immune System Diseases / epidemiology*
  • Immune System Diseases / etiology
  • Immunotherapy / adverse effects*
  • Japan / epidemiology
  • Lung Neoplasms / epidemiology
  • Lung Neoplasms / immunology
  • Lung Neoplasms / therapy*
  • Male
  • Middle Aged
  • Retrospective Studies
  • Risk Factors
  • Tumor Burden

Substances

  • Antibodies, Monoclonal
  • Costimulatory and Inhibitory T-Cell Receptors