Retrospective Analysis of Bevacizumab in Combination with Fotemustine in Chinese Patients with Recurrent Glioblastoma Multiforme

被引:3
|
作者
Liu, Zhiguang [1 ]
Zhang, Guanqun [1 ]
Zhu, Liang [1 ]
Wang, Jiangbo [1 ]
Liu, Dongbo [2 ]
Lian, Lifei [3 ]
Liu, Jianlin [3 ]
Lai, Tianbao [4 ]
Zhuang, Xiaorong [4 ]
机构
[1] Xuzhou Ctr Hosp, Dept Neurol, Xuzhou 221009, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Dept Canc, Wuhan 430030, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Dept Neurol, Wuhan 430030, Peoples R China
[4] Xiamen Univ, Zhongshan Hosp, Dept Neurol, Xiamen 361004, Peoples R China
关键词
DOSE-INTENSE TEMOZOLOMIDE; SINGLE-AGENT BEVACIZUMAB; PHASE-II TRIAL; PROGNOSTIC-FACTORS; PLUS IRINOTECAN; ADJUVANT TEMOZOLOMIDE; PROMOTER METHYLATION; RADIATION-THERAPY; RADIOTHERAPY; PROGRESSION;
D O I
10.1155/2015/723612
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The aim of this study was to assess the activity and safety of bevacizumab (BEV) and fotemustine (FTM) for the treatment of recurrent glioblastoma multiforme (GBM) patients and explore the potential prognostic parameters on survival. This study retrospectively analyzed all patients with GBM who were treated with at least one cycle of BEV and FTM from July 2010 to October 2012. A total of 176 patients with recurrent GBM were enrolled. The response rate and disease control rate were 46.6% and 90.9%, respectively. A 6-month PFS rate of 33.3% (95% CI: 26.5%-40.3%) and a median PFS of 5.0 (95% CI: 2.4-7.5) months were observed. The median OS was 8.0 (95% CI: 6.7-9.2) months. Multivariate analysis showed that risk factors with a significant influence on the PFS of all patients were Karnofsky Performance Status (KPS) (>= 70 versus <70, HR = 0.53, 95% CI: 0.39-0.73, and P = 0.01) and MGMT status (methylated versus unmethylated, HR = 0.69, 95% CI: 0.52-0.97, and P = 0.04). The most common treatment-related adverse events were fatigue, proteinuria, hypophonia, hypertension, thrombocytopenia, anemia, and neutropenia. In conclusion, combination of BEV with FTM is well tolerated and may derive some clinical benefits in recurrent GBM patients. Higher KPS and MGMT promoter hypermethylation were suggested to be associated with prolonged survival.
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页数:8
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