单药贝伐单抗治疗福莫司汀二线化疗后复发的胶质母细胞瘤:意大利神经肿瘤协会的经验。

Francesco Pasqualetti, Andrea Pace, Alessandra Gonnelli, Veronica Villani, Martina Cantarella, Durim Delishaj, Caterina Vivaldi, Alessandro Molinari, Sabrina Montrone, Alessia Pellerino, Federica Franchino, Davide Baldaccini, Giuseppe Lombardi, Ivan Lolli, Francesca Catania, Elena Bazzoli, Riccardo Morganti, Alessandra Fabi, Vittorina Zagonel, Guido Bocci, Maria Grazia Fabrini, Roberta Rudà, Riccardo Soffietti, Fabiola Paiar
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引用次数: 3

摘要

目的:贝伐单抗是一种抗血管内皮生长因子抗体,用于治疗复发性胶质母细胞瘤(GBM)。尽管在复发性GBM患者中进行了大量的研究,但对二线化疗失败后这种血管生成抑制剂的使用知之甚少。材料和方法:在这项多中心回顾性研究中,我们代表意大利神经肿瘤协会,报告了51例复发性GBM患者在使用福替莫司汀二线化疗失败后,使用单药贝伐单抗治疗的结果。结果:2016年3月,数据分析时,3例患者(14.4%)病情稳定存活,48例因疾病进展死亡。Kaplan-Meier估计,诊断为GBM后的中位生存期为28个月(95%可信区间[CI], 22.1-33.9个月)。从福莫司汀和贝伐单抗治疗开始的中位生存期分别为11.3个月(95% CI, 8.4-13.6个月)和6个月(95% CI, 3.8-8.1个月)。贝伐单抗治疗开始后的6个月和12个月无进展生存率分别为18%和13%。结论:根据我们的数据,在复发性GBM患者中,使用细胞毒性药物的二线化疗失败可能不排除贝伐单抗作为三线化疗的使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single-agent Bevacizumab in Recurrent Glioblastoma After Second-line Chemotherapy With Fotemustine: The Experience of the Italian Association of Neuro-Oncology.

Objectives: Bevacizumab is an anti-vascular endothelial growth factor antibody used in the treatment of recurrent glioblastoma (GBM). Despite the large number of studies carried out in patients with recurrent GBM, little is known about the administration of this angiogenesis inhibitor after the failure of the second-line chemotherapy.

Materials and methods: In this retrospective multicenter study, on behalf of the Italian Association of Neuro-Oncology, we reported the results obtained in 51 patients with recurrent GBM treated with single-agent bevacizumab after the failure of second-line chemotherapy with fotemustine.

Results: In March 2016, at the time of data analysis, 3 patients (14.4%) were still alive with stable disease, whereas 48 died due to disease progression. Kaplan-Meier estimated median survival from the diagnosis of GBM was 28 months (95% confidence interval [CI], 22.1-33.9 mo). Median survival measured from the beginning of fotemustine and bevacizumab therapy were 11.3 (95% CI, 8.4-13.6 mo) and 6 months (95% CI, 3.8-8.1 mo), respectively. The 6- and 12-month progression free survival rates from the beginning of bevacizumab treatment were 18% and 13%, respectively.

Conclusions: On the basis of our data, in patients with recurrent GBM, the failure of a second-line chemotherapy with cytotoxic agents might not exclude the administration of bevacizumab as third-line chemotherapy.

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