Complex renal cysts associated with crizotinib treatment

Patrick Schnell1, Cynthia H Bartlett1, Benjamin J Solomon2

  • 1Pfizer Oncology, New York, New York.

Cancer Medicine
|March 11, 2015
PubMed

Insights

Crizotinib treatment for anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer (NSCLC) is associated with increased renal cyst development. Monitoring is advised, but dose adjustments are usually not needed, allowing continued patient benefit.

Area of Science:

  • Oncology
  • Pharmacology
  • Radiology

Background:

  • Crizotinib is a targeted therapy for anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer (NSCLC).
  • Clinical trials observed an association between crizotinib and renal cyst development.

Purpose of the Study:

  • To investigate the association between crizotinib treatment and renal cyst development in ALK-positive NSCLC patients.
  • To assess the incidence, characteristics, and risk factors of renal cysts during crizotinib therapy.

Main Methods:

  • Reviewed serious adverse event (SAE) reports of renal cysts from 1375 patients across four clinical trials.
  • Conducted a blinded, retrospective, independent radiologic review (IRR) of scans from 255 crizotinib-treated patients on study for ≥ 6 months.
  • Assessed risk factors, including ethnicity, for renal cyst development.

Main Results:

  • Among 17 patients with renal cysts reported as SAEs, seven showed invasion into adjacent structures without malignancy; most continued crizotinib without dose modification.
  • In the IRR, 22% had preexisting simple cysts, 3% complex cysts, and 2% both.
  • At 6 months, 9% of patients acquired new cysts, and 2% with preexisting cysts experienced new cysts or enlargements; Asians, particularly Koreans, showed a higher risk (OR 5.18).

Conclusions:

  • Crizotinib treatment is associated with an increased risk of renal cyst development and progression in ALK-positive NSCLC patients.
  • Close monitoring for renal cysts is recommended during crizotinib therapy.
  • Dosing modifications were generally not required, enabling continued treatment and clinical benefit for most patients.

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