Rechallenge with bevacizumab in patients with glioblastoma progressing off therapy

被引:0
|
作者
Charlotte Bronnimann
Cristina Izquierdo
Stéphanie Cartalat
Laure Thomas
Bastien Joubert
Laura Delpech
Marc Barritault
David Meyronet
Jérôme Honnorat
François Ducray
机构
[1] Hospices Civils de Lyon,Department of Cancer Cell Plasticity
[2] Groupe Hospitalier Est,Institut NeuroMyoGene
[3] Service de Neuro-Oncologie,undefined
[4] Université Claude Bernard Lyon 1,undefined
[5] Cancer Research Centre of Lyon,undefined
[6] INSERM U1052,undefined
[7] CNRS UMR5286,undefined
[8] Hospices Civils de Lyon,undefined
[9] Groupe Hospitalier Est,undefined
[10] Service de Neuropathologie,undefined
[11] Hospices Civils de Lyon,undefined
[12] Groupe Hospitalier Est,undefined
[13] Service de Neuro-Oncologie,undefined
[14] INSERM 1217/CNRS 5310,undefined
[15] Université de Lyon,undefined
来源
Journal of Neuro-Oncology | 2018年 / 138卷
关键词
Bevacizumab; Rechallenge; Glioblastoma; Therapy;
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学科分类号
摘要
Rechallenge with temozolomide has been shown to be a valid option in selected patients with progressive glioblastoma. Herein, we assessed the efficacy of rechallenge with bevacizumab in glioblastoma patients progressing off therapy. We retrospectively identified and analyzed the characteristics of patients with glioblastoma rechallenged with a bevacizumab-based chemotherapy regimen after having received bevacizumab as first-line treatment in association with temozolomide radiochemotherapy or at recurrence in association with temozolomide, CCNU or irinotecan. Twenty-five patients were identified. In all included patients, the first bevacizumab treatment resulted in an objective response and was discontinued for reasons other than disease progression (adverse event n = 9, physician or patient decision n = 16). Median duration of first bevacizumab treatment was 6 months (range: 2–58 months). None of the patients presented a rebound effect after bevacizumab discontinuation. The median interval between discontinuation of first bevacizumab treatment and bevacizumab rechallenge was 8.9 months (range: 2–58 months). At this time, bevacizumab was given in association with lomustine (n = 17), temozolomide (n = 6), irinotecan (n = 1), or alone (n = 1). Bevacizumab rechallenge resulted in an objective response in 15 patients (60%). Median progression-free survival was 6.7 months and overall survival was 9.6 months after bevacizumab rechallenge. Timing of first bevacizumab treatment (as first-line treatment or at recurrence) was not associated with the duration of response after treatment rechallenge. In the present series, patients who responded to bevacizumab and in whom this treatment was discontinued in the absence of tumor progression seemed to benefit from rechallenge with a bevacizumab-based chemotherapy regimen.
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页码:141 / 145
页数:4
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