Pazopanib-associated interstitial lung disease in a patient with renal cell carcinoma

Yukinori Harada1, Shintaro Kakimoto1, Taro Shimizu2

  • 1Department of Diagnostic and Generalist Medicine, Dokkyo Medical University Hospital, Shimotsuga-gun, Tochigi, Japan.

BMJ Case Reports
|July 10, 2020
PubMed

Insights

Pazopanib, a cancer drug, can rarely cause interstitial lung disease. This case highlights the importance of recognizing this adverse effect in patients with renal cell carcinoma or soft-tissue sarcoma.

Area of Science:

  • Oncology
  • Pulmonology
  • Pharmacology

Background:

  • Pazopanib is a multi-targeted tyrosine kinase inhibitor used for advanced renal cell carcinoma and soft-tissue sarcomas.
  • Interstitial lung disease (ILD) is a rare but serious adverse event associated with pazopanib therapy.

Observation:

  • A 75-year-old male patient developed ILD three months after starting pazopanib for renal cell carcinoma with lung metastases.
  • Symptoms included dry cough, fatigue, hypoxia, and bilateral ground-glass opacities on chest CT.
  • The patient's condition worsened despite antibiotic treatment, necessitating non-invasive ventilation.

Findings:

  • Discontinuation of pazopanib and administration of systemic steroids led to the patient's recovery.
  • This case demonstrates a clear link between pazopanib treatment and the development of ILD.

Implications:

  • Clinicians must maintain a high index of suspicion for ILD in patients receiving pazopanib.
  • Early recognition and prompt management, including drug cessation, are crucial for favorable outcomes.
  • This underscores the need for careful monitoring of pulmonary function in patients undergoing pazopanib treatment.

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