Dose Escalation of Imatinib After Failure of Standard Dose in Korean Patients with Metastatic or Unresectable Gastrointestinal Stromal Tumor

被引:18
|
作者
Park, Inkeun [1 ]
Ryu, Min-Hee [1 ]
Sym, Sun Jin [1 ]
Lee, Sung Sook [1 ]
Jang, Geundoo [1 ]
Kim, Tae Won [1 ]
Chang, Heung Moon [1 ]
Lee, Jae-Lyun [1 ]
Lee, Hyoungnam [1 ]
Kang, Yoon-Koo [1 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Internal Med,Div Oncol, Seoul 138736, South Korea
关键词
OF-FUNCTION MUTATIONS; ACTIVATING MUTATIONS; C-KIT; PROGRESSION; MESYLATE; EFFICACY; SAFETY; GENE;
D O I
10.1093/jjco/hyn134
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We evaluated the results of imatinib dose escalation in patients with advanced gastrointestinal stromal tumors (GISTs) after disease progression on standard-dose imatinib. Clinical data from patients with metastatic or unresectable GISTs whose dose of imatinib was increased after disease progression on imatinib 400 mg/day were retrospectively reviewed. The 24 patients studied had a median age of 52 years. Imatinib dosing was escalated to 600 mg/day in 12 patients, then to 800 mg/day in four patients. The other 12 patients had dose escalation directly to 800 mg/day. Two patients (8.3%) achieved a partial response, and seven (29.2%) had stable disease. Six-month progression-free and overall survival rates were 33.3 and 70.7%, respectively. Dose escalation to 600 or 800 mg/day was generally well tolerated. Imatinib dose escalation is feasible and well tolerated in patients with advanced GIST who progress on standard-dose therapy, producing clinical benefit in similar to 37% of patients.
引用
收藏
页码:105 / 110
页数:6
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