Purpose
To detail tolerance of temsirolimus in a routine practice setting within a compassionate use program for patients with renal
cell carcinoma.
Methods
We treated 32 patients with advanced renal cell carcinoma with temsirolimus within the German compassionate use program on
an individual patient basis free of charge according to EU guidelines at our two institutions. Twenty-five milligrams of temsirolimus
was applied weekly in an inpatient clinical setting. Adverse events were classified following National Cancer Institute Common
Toxicity Criteria.
Results
No dose modification or therapy interruptions were necessary due to adverse events. Adverse events like asthenia/fatigue were
observed in 43.8%, increased creatinine in 40.6%, mucositis in 31.3%, secondary diabetes in 28.1%, hypothyreosis in 12.5%
and rash in 12.5%, hypercholesterolemia and hypertriglyceridemia in 9.3% of the patients.
Conclusion
Therapy with temsirolimus in advanced renal cell carcinoma is well tolerated. In a routine practice setting it results in
a predictable adverse event profile that can be managed medically.
Keywords Adverse event management - Compassionate use program - Renal cell carcinoma - Temsirolimus