Add-on bevacizumab can prevent early clinical deterioration and prolong survival in newly diagnosed partially resected glioblastoma patients with a poor performance status

被引:14
作者
Hata, Nobuhiro [1 ,2 ]
Yoshimoto, Koji [1 ]
Hatae, Ryusuke [1 ]
Kuga, Daisuke [1 ]
Akagi, Yojiro [1 ]
Sangatsuda, Yuhei [1 ]
Suzuki, Satoshi O. [3 ]
Shono, Tadahisa [1 ,4 ]
Mizoguchi, Masahiro [1 ,5 ]
Iihara, Koji [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Neurosurg, Fukuoka, Japan
[2] Natl Hosp Org, Kyushu Med Ctr, Clin Res Inst, Dept Neurosurg, Fukuoka, Japan
[3] Kyushu Univ, Grad Sch Med Sci, Dept Neuropathol, Fukuoka, Japan
[4] Harasanshin Hosp, Dept Neurosurg, Fukuoka, Japan
[5] Kitakyushu Municipal Med Ctr, Dept Neurosurg, Kitakyushu, Fukuoka, Japan
来源
ONCOTARGETS AND THERAPY | 2017年 / 10卷
关键词
bevacizumab; glioblastoma; performance status; survival; unresectable; HIGH-GRADE GLIOMAS; RADIOTHERAPY; TEMOZOLOMIDE; THERAPY; DISCONTINUATION; AVAGLIO; TRIAL;
D O I
10.2147/OTT.S125587
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
Purpose: The AVAglio trial established the beneficial effect of add-on bevacizumab (BEV) for the treatment of newly diagnosed glioblastomas (nd-GBMs) that led to the approval of BEV for the treatment of these patients in Japan. However, the rationality of using BEV as a first-line treatment for nd-GBMs remains controversial. The purpose of this study was to analyze the outcomes of a case series of nd-GBM patients. Patients and methods: The outcomes of 69 nd-GBM patients treated after 2006 were retrospectively analyzed. Clinical and genetic analyses were performed, and estimates of progression-free survival (PFS) and overall survival (OS) were calculated using the Kaplan-Meier method. Since add-on BEV therapy was only used for partially resected GBMs (pr-GBMs) after its approval in 2013, the patients were subdivided into 3 treatment groups: Type I, partial removal with temozolomide (TMZ)/BEV and concurrent radiotherapy (CCRT); Type II, partial removal with TMZ and CCRT; and Type III, gross total removal with TMZ and CCRT. Results: The PFS rate of Type I patients was significantly higher than that of Type II patients (P= 0.014), but comparable to that of Type III patients. Differences in OS rates between Type I and Type II patients were less apparent (P= 0.075), although the median OS of Type I patients was similar to 8 months higher than that of Type II patients (17.4 vs 9.8 months, respectively). The clinical deterioration rate during initial treatment was significantly (P= 0.024) lower in Type I than in Type II patients (7.7% vs 47.4%, respectively). Differences in OS rates between Type I and Type II patients with a poor performance status (PS) were significant (P= 0.017). Conclusion: Our findings suggest that add-on BEV can prevent early clinical deterioration of pr-GBM patients and contribute to a prolonged survival, especially for those with a poor PS.
引用
收藏
页码:429 / 437
页数:9
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