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Managing pazopanib toxicity in the treatment of advanced soft tissue sarcoma

Authors :
Boccone, Paola
Laera, Letizia
Baldi, Giacomo Giulio
Miano, Sara
Aliberti, Sandra
Tolomeo, Francesco
D’Ambrosio, Lorenzo
Grignani, Giovanni
Boccone, Paola
Laera, Letizia
Baldi, Giacomo Giulio
Miano, Sara
Aliberti, Sandra
Tolomeo, Francesco
D’Ambrosio, Lorenzo
Grignani, Giovanni
Source :
Cancer Breaking News; Vol. 4 No. 3 (2016): December 2016; 30-35; 2283-6594
Publication Year :
2016

Abstract

Background Pazopanib is a multikinase inhibitor registered for the treatment of advanced renal clear cell carcinoma (RCC) and as second or further-line therapy in advanced non-adipocytic soft tissue sarcoma (STS). It is a relatively well-tolerated compound, but, as with many other tyrosine kinase inhibitors (TKI), chronic toxicity may become a challenge that both patient and physician need to take into account when starting treatment. This retrospective study investigated toxicities and their management in STS patients treated with pazopanib in routine clinical practice in Italy. Materials and Methods Data were collected between January 2013 and May 2016 at Candiolo Cancer Institute and Prato Medical Oncology Unit. The primary objective was to describe observed toxicities in a real-life setting, and use this information to inform strategies for adverse event management. Results A total of 43 patients with advanced STS who received treatment with pazopanib were included. Median progression-free survival was 4 months and median overall survival was 18 months. The most common toxicities were fatigue (74.4%), hypertension (72%), hair hypopigmentation (74.4%) and diarrhea (60.5%). Liver toxicities occurred in less than one-third of patients. Severe adverse events, requiring drug interruption, were relatively rare. Conclusions This study confirms the safety and efficacy of pazopanib in pretreated unresectable or metastatic soft tissue sarcoma, and highlights the importance of close follow-up and patient support to improve compliance and treatment duration.

Details

Database :
OAIster
Journal :
Cancer Breaking News; Vol. 4 No. 3 (2016): December 2016; 30-35; 2283-6594
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1432705941
Document Type :
Electronic Resource