Outcomes of salvage fractionated re-irradiation combined with bevacizumab for recurrent high-grade gliomas that progressed after bevacizumab treatment

被引:5
|
作者
Yonezawa, Hajime [1 ]
Ohno, Makoto [1 ]
Igaki, Hiroshi [2 ]
Miyakita, Yasuji [1 ]
Takahashi, Masamichi [1 ]
Tamura, Yukie [1 ]
Shima, Satoshi [2 ]
Matsushita, Yuko [1 ]
Ichimura, Koichi [3 ]
Narita, Yoshitaka [1 ]
机构
[1] Natl Canc Ctr, Dept Neurosurg & Neurooncol, Tokyo, Japan
[2] Natl Canc Ctr, Dept Radiat Oncol, Tokyo, Japan
[3] Natl Canc Ctr, Div Brain Tumor Translat Res, Tokyo, Japan
关键词
bevacizumab; disease progression; glioma; re-irradiation; treatment failure; STEREOTACTIC RADIOSURGERY; CONCURRENT BEVACIZUMAB; MALIGNANT GLIOMAS; PHASE-II; GLIOBLASTOMA; EFFICACY; PATTERNS; THERAPY; FAILURE; SAFETY;
D O I
10.1093/jjco/hyab063
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: There is no standard treatment for patients with recurrent high-grade gliomas who progress after bevacizumab treatment. We evaluated the outcomes of re-irradiation combined with bevacizumab for patients refractory to bevacizumab. Methods: Between January 2015 and September 2019, patients with progression after bevacizumab treatment were treated with re-irradiation combined with bevacizumab (25 Gy in five fractions). Results: Fourteen patients [glioblastoma, isocitrate dehydrogenase (IDH) wild type (N = 6), glioblastoma, IDH mutant (N = 4), anaplastic astrocytoma, IDH wild type (N = 1), anaplastic astrocytoma, IDH mutant (N = 1), glioblastoma, not otherwise specified (N = 1) and radiologically diagnosed brainstem glioma (N = 1)] were included in this study. The median survival and progression-free survival times after re-irradiation combined with bevacizumab were 6.1 and 3.8 months, respectively. The 6-month survival and progression-free survival rates were 54.5 and 15.7%, respectively. Patients with a Karnofsky performance status of >= 70 tended to have longer median survival time (9.3 vs. 5.4 months, respectively; P = 0.058) and had a significantly longer median progression-free survival time (4.2 vs. 3.7 months, respectively; P = 0.046) than those with a Karnofsky performance status of <70. Four patients (28.6%) achieved a complete or partial radiological response, and three patients (21.4%) had an improved Karnofsky performance status after re-irradiation combined with bevacizumab. Grade 3/4 toxicities included leukopenia in four patients (28.6%), hypertension in three (21.4%), proteinuria in one (7.1%) and gastrointestinal hemorrhage in one (7.1%). Conclusions: Re-irradiation combined with bevacizumab for patients with recurrent high-grade gliomas who progress after bevacizumab treatment was feasible. Re-irradiation combined with bevacizumab is a potential treatment option, especially for patients with a Karnofsky performance status of >= 70.
引用
收藏
页码:1028 / 1035
页数:8
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