Clinical Impact of Bevacizumab in Patients with Relapsed Glioblastoma: Focus on a Real-Life Monocentric SurVey (SV1 Study)

被引:1
作者
Rivoirard, Romain [1 ]
Chargari, Cyrus [6 ]
Guy, Jean-Baptiste [2 ]
Nuti, Christophe [3 ]
Peoc'h, Michel [4 ]
Forest, Fabien [4 ]
Falk, Alexander Tuan [7 ]
Garin, Clemence [2 ]
Adjabi, Anissa [2 ]
Hoarau, Delphine [2 ]
Fotso, Marie-Jeannette [3 ]
Escure, Julien Langrand [2 ]
Moriceau, Guillaume [1 ]
Fournel, Pierre [1 ]
Boutet, Claire [5 ]
Magne, Nicolas [2 ]
机构
[1] CHU St Etienne, Dept Med Oncol, St Priest En Jarez, France
[2] CHU St Etienne, Dept Radiotherapy, Inst Cancerol Lucien Neuwirth, St Priest En Jarez, France
[3] CHU St Etienne, Dept Neurosurg, St Priest En Jarez, France
[4] CHU St Etienne, Anatomopathol Lab, St Priest En Jarez, France
[5] CHU St Etienne, Serv Radiol, St Priest En Jarez, France
[6] Hop Instruct Armees Val de Grace, Dept Med Oncol & Radiotherapy, Paris, France
[7] Ctr Antoine Lacassagne, Dept Radiat Oncol, Nice, France
关键词
Bevacizumab; Efficacy; Irinotecan; Relapsed glioblastoma; Safety; PHASE-II TRIAL; RECURRENT MALIGNANT GLIOMA; SINGLE-AGENT BEVACIZUMAB; HIGH-GRADE GLIOMAS; RADIATION-THERAPY; PLUS IRINOTECAN; TEMOZOLOMIDE; RADIOTHERAPY; COMBINATION; MULTIFORME;
D O I
10.1159/000443719
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Glioblastoma is one of the most frequent primitive brain tumors. Patients who experience tumor relapse after surgery and concomitant radiochemotherapy have a dismal prognosis. The objective of this study is to analyze efficacy data in terms of overall survival (OS) and progressionfree survival (PFS) following combination therapy with bevacizumab (BVZ) and irinotecan among patients with relapsed glioblastoma. Safety data will also be reviewed and all results will be compared with data of the literature. Methods: In this single-center retrospective study, all records of patients treated with BVZ and irinotecan for a relapsed glioblastoma were analyzed. Each chemotherapy cycle was repeated every 15 days until progression. Magnetic resonance imaging and neurologic examination were repeated every 6 weeks during treatment. Results: Forty-five patients were analyzed. The median number of BVZ-irinotecan cycles was 8 (range 1-38). Median PFS was 26 weeks and median OS was 28 weeks. Eighteen of the 45 patients (40% of cases) had an objective response 6 months after initiation of treatment. Two patients had to discontinue treatment due to toxicity. Conclusions: The results of the SV1 study are consistent with those found in phase II studies evaluating the same treatment. The irinotecan-BVZ combination is effective in relapsed glioblastoma with acceptable toxicity. Biomarkers predictive of response to BVZ should help in the selection of patients who could benefit from treatment. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:269 / 274
页数:6
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