Hypereosinophilia in a patient with metastatic non-small-cell lung cancer treated with antiprogrammed cell death 1 (anti-PD-1) therapy

Immunotherapy. 2019 May;11(7):577-584. doi: 10.2217/imt-2018-0128.

Abstract

Immune checkpoint inhibitors have changed the treatment paradigm for patients with cancer. Though a majority of patients tolerate treatment, some develop hematologic toxicities, including eosinophilia. Eosinophilia has been associated with better responses in some patients with melanoma, but this has not been investigated in non-small-cell lung cancer. We present a case of a woman with metastatic lung adenocarcinoma who developed asymptomatic hypereosinophilia after initiation of nivolumab. Her eosinophil count temporarily decreased after transiently stopping the medication, but increased again after re-initiation. She had a favorable tumor response to therapy. This exemplifies the potential role of eosinophilia as a peripheral, readily available biomarker of favorable response to immunotherapy in patients with lung cancer. Awareness of this manifestation is important.

Keywords: biomarker; hypereosinophilia; immune-related adverse events; lung cancer; nivolumab.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / therapeutic use*
  • Biomarkers, Pharmacological
  • Carcinoma, Non-Small-Cell Lung / diagnosis
  • Carcinoma, Non-Small-Cell Lung / drug therapy*
  • Drug-Related Side Effects and Adverse Reactions / diagnosis*
  • Eosinophilia / diagnosis*
  • Eosinophilia / etiology
  • Female
  • Humans
  • Immunotherapy / adverse effects
  • Immunotherapy / methods*
  • Lung Neoplasms / diagnosis
  • Lung Neoplasms / drug therapy*
  • Neoplasm Metastasis
  • Neoplasm Staging
  • Nivolumab / adverse effects
  • Nivolumab / therapeutic use*
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • Biomarkers, Pharmacological
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • Nivolumab