Sunitinib in metastatic renal cell carcinoma: An ethnic Asian subpopulation analysis for safety and efficacy

被引:36
作者
Lee, Se-Hoon [1 ,2 ]
Bang, Yung-Jue [1 ,2 ]
Mainwaring, Paul [4 ]
Ng, Christina [5 ]
Chang, John W-C [6 ,7 ]
Kwong, Philip [8 ]
Li, Rubi K. [9 ]
Sriuranpong, Virote [10 ]
Toh, Chee-Keong [11 ]
Yuan, Jinyu [12 ]
Pitman Lowenthal, Susan [12 ]
Chung, Hyun C. [3 ]
机构
[1] Seoul Natl Univ Hosp, Dept Internal Med, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul 110744, South Korea
[3] Yonsei Univ, Coll Med, Yonsei Canc Ctr, Yonsei Univ Hlth Syst, Seoul, South Korea
[4] Mater Adult Hosp, South Brisbane, Qld, Australia
[5] Univ Malaya, Dept Med, Med Ctr, Kuala Lumpur, Malaysia
[6] Chang Gung Mem Hosp, Div Hematol Oncol, Dept Internal Med, Taoyuan, Taiwan
[7] Chang Gung Univ, Coll Med, Taoyuan, Taiwan
[8] Queen Mary Hosp, Dept Clin Oncol, Hong Kong, Hong Kong, Peoples R China
[9] St Lukes Med Ctr, Canc Inst, Quezon City, Philippines
[10] Chulalongkorn Univ, Fac Med, Med Oncol Unit, Dept Med, Bangkok 10330, Thailand
[11] Natl Canc Ctr, Dept Med Oncol, Singapore, Singapore
[12] Pfizer Oncol, New York, NY USA
关键词
Asian; metastatic renal cell carcinoma; sunitinib; ENDOTHELIAL GROWTH-FACTOR; TYROSINE KINASE INHIBITOR; INTERFERON-ALPHA; JAPANESE PATIENTS; FACTOR RECEPTOR; PHASE-II; SU11248; SURVIVAL; TOXICITY; CANCER;
D O I
10.1111/ajco.12163
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: We evaluated and compared the safety and efficacy of sunitinib in Asian and non-Asian patients with metastatic renal cell carcinoma enrolled in a previously reported global expanded access program. Methods: Previously treated and treatment-naive patients received open-label sunitinib at a starting dose of 50 mg/day for 4 weeks, followed by 2 weeks off treatment, in repeated 6-week cycles. Safety was assessed regularly, tumor measurements were performed per local practice, and survival data collected where possible. Results: Data were available for 212 Asian patients from Asian sites (Asian-A), 113 Asian patients from non-Asian sites (Asian-O) and 4046 non-Asian patients. The most common grade 3/4 treatment-related adverse events were neutropenia, thrombocytopenia, hand-foot syndrome, diarrhea, asthenia and fatigue. The incidence of many adverse events was greater in Asian-A than in Asian-O or non-Asian patients. Sunitinib efficacy was comparable between Asian and non-Asian patients, with an objective response rate of 18% versus 14%; median progression-free survival of 8.7 versus 10.9 months; and overall survival of 18.9 versus 18.4 months, respectively. Conclusions: Sunitinib demonstrated tolerable safety and similar efficacy in Asian and non-Asian patients. Geographic differences in the reported frequency of specific adverse events were noted across Asian patients.
引用
收藏
页码:237 / 245
页数:9
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