Hand–foot skin reaction predicts treatment outcome of pazopanib in patients with metastatic soft tissue sarcoma: A multicenter study in the Asian population. Issue 4 (13th June 2018)

• Record Type: Journal Article
• Authors: Huang, Pei‐Wei; Chou, Wen‐Chi; Shen, Wen‐Chi; Hung, Chia‐Yen; Huang, Kuan‐Gen; Su, Yu‐Li; Lu, Chang‐Hsien; Liu, Chien‐Ting; Chang, Yueh‐Shih; Liau, Chi‐Ting
• Is Part Of: Asia-Pacific journal of clinical oncology. Volume 14:Issue 4(2018)
• Page Start: 353
• Page End: 360
• Publication Date: 2018-06-13
• Subjects: chemotherapy‐refractory sarcoma -- hand–foot skin reaction -- pazopanib -- soft tissue sarcoma -- tyrosine kinase inhibitor; Oncology -- Pacific Area -- Periodicals; Cancer -- Treatment -- Pacific Area -- Periodicals; Cancer -- Pacific Area -- Periodicals; Cancer -- Treatment -- Periodicals; 616.9940095
• DOI: 10.1111/ajco.13029
• Languages: English
• ISSNs: 1743-7555

Abstract

Abstract: Aim: Pazopanib is a multitargeted tyrosine kinase inhibitor used as a standard treatment for chemotherapy‐refractory recurrent or metastatic soft tissue sarcoma. This study aimed to evaluate the efficacy and safety of pazopanib for treatment of metastatic soft tissue sarcoma in the Asian population. Methods: Fifty patients with chemotherapy‐refractory recurrent or metastatic soft tissue sarcoma, who had received pazopanib treatment between 2015 and 2016 were enrolled. We reviewed patients' clinical characteristics and studied survival outcomes following pazopanib treatment. Results: Median follow‐up was 5.7 months. Seven patients were still on pazopanib by the end of this study and the disease had progressed in the other 43 patients, leading to 23 deaths. We found that despite treatment more than half the patients experienced disease progression (56% vs 14% partial response and 30% stable disease). The median progression‐free survival and overall survival was 3.1 and 11.0 months, respectively. Multivariate analysis identified good Eastern Cooperative Oncology Group performance status (0 or 1) and occurrence of hand–foot skin reaction as independent factors associated with better outcome. Hand–foot skin reaction was 32% in our cohort and the median onset time was 4 (1.00–8.29) weeks. It had dose‐dependent effect by clinical observation. Conclusions: Our study showed that the incidence rate of hand–foot skin reaction in Taiwan is higher than western population, and it is an independent predictive factor for better treatment outcomes.