Interstitial pneumonitis associated with leuprorelin acetate for a prostate cancer: A case report

J Oncol Pharm Pract. 2022 Dec;28(8):1910-1913. doi: 10.1177/10781552221084058. Epub 2022 Mar 2.

Abstract

Introduction: Androgen deprivation therapy remains the essential treatment for disseminated prostate cancer. Interstitial pneumonitis following this therapy has been documented for just a few cases. However, reported cases frequently describe the onset of symptoms after recent administration (days or a few weeks) of both GnRH analogues and androgen antagonists, which makes the precise individual impact of each treatment difficult to estimate.

Case report: This report presents a case of a 94-year-old patient with interstitial pneumonitis whose onset started three months after the first dose of leuprorelin and bicalutamide for a metastatic prostate cancer.

Management and outcome: Once other possible diagnosis were ruled out, empiric corticosteroid treatment was initiated within 48 h of the admission. A spectacular clinical and radiological improvement was observed after 3 doses of steroids, enabling the patient to recover his basal respiratory situation. We considered that the most probable cause was toxic interstitial pneumonitis induced by leuprorelin.

Discussion: To our knowledge, it describes the longest interval between last administration of antiandrogen therapy and the development of pneumonitis. This fact may support a direct relation with leuprorelin, whose serum levels remain high for months because of its long-acting depot formulation.

Keywords: Interstitial pneumonitis; antiadrogen therapy; prostate cancer; pulmonary toxicity.

Publication types

  • Case Reports

MeSH terms

  • Acetates / therapeutic use
  • Aged, 80 and over
  • Androgen Antagonists / adverse effects
  • Antineoplastic Agents, Hormonal / adverse effects
  • Humans
  • Leuprolide / adverse effects
  • Lung Diseases, Interstitial* / chemically induced
  • Male
  • Prostatic Neoplasms* / pathology

Substances

  • Leuprolide
  • Androgen Antagonists
  • Acetates
  • Antineoplastic Agents, Hormonal