The purpose of this study is to evaluate the safety and efficacy of Cabozantinib in the treatment of patients with renal cell carcinoma.
Study Type
OBSERVATIONAL
Enrollment
100
The regimen will be a single oral dose administered daily on a continuous schedule, taken with or without food. The standard dose is 60 mg per day, which can be reduced to 40 or 20 mg according to the latest version of the Summary of Product Characteristics-SPC available. The treating oncologist will evaluate the opportunity to prudentially start treatment at 40 mg/daily in patients screening positively at G8 screening tool, and then escalate to 60 mg/daily only in case of absence of toxicity ³grade 2 at subsequent cycles. Temporary suspensions of treatment are allowed according to the local practice and will be registered if ³ 7 days.
Istituto Oncologico Veneto
Padova, Italy, Italy
Clinical tolerability of Cabozantinib
the main purpose is to register the Incidence of Treatment-Emergent Adverse Events \[Safety and Tolerability\]
Time frame: Average of 1 year
Description of response rate of patients treated with Cabozantinib.
according to RECIST criteria, only patients with measurable disease will be evaluated for response
Time frame: From date of randomization until the date of last documented, assessed up to 18 months"
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.