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阿帕替尼用于复发性/进展性多形性胶质母细胞瘤:一种挽救性选择。

Apatinib for recurrent/progressive glioblastoma multiforme: A salvage option.

作者信息

Zhang Hong-Hong, Du Xiao-Jing, Deng Mei-Ling, Zheng Lie, Yao Dun-Chen, Wang Zhi-Qiang, Yang Qun-Ying, Wu Shao-Xiong

机构信息

Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, China.

Department of Radiation Oncology, Xiang'an Hospital of Xiamen University, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, China.

出版信息

Front Pharmacol. 2022 Aug 17;13:969565. doi: 10.3389/fphar.2022.969565. eCollection 2022.

Abstract

The recurrent/progressive glioblastoma multiforme (GBM) carries a dismal prognosis and the definitive treatment strategy has not yet been established. This study aimed to assess the efficacy and safety of apatinib in recurrent/progressive GBM patients. The clinical data of 19 recurrent/progressive GBM patients who received apatinib treatment from November 2015 to December 2019 at Sun Yat-sen University Cancer Center were collected retrospectively in this study. Objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and treatment-related adverse events (AEs) were reviewed and assessed. The overall ORR was 52.6%, and the DCR was 73.7%. Median PFS and OS were 5.1 and 10.4 months, respectively. The 6-month PFS and OS rates were 38.9% and 68.4%, respectively. The 12-month PFS and OS rates were 16.7% and 36.8%, respectively. The treatment-related toxicities were generally well-tolerated. The most common grade 3/4 AEs were hand-foot syndrome (36.8%) and hypertension (21.1%). Our study showed that apatinib therapy provided a better salvaging option for recurrent/progressive GBM patients and the toxicity was manageable.

摘要

复发性/进展性多形性胶质母细胞瘤(GBM)预后不佳,目前尚未确立明确的治疗策略。本研究旨在评估阿帕替尼治疗复发性/进展性GBM患者的疗效和安全性。本研究回顾性收集了2015年11月至2019年12月在中山大学肿瘤防治中心接受阿帕替尼治疗的19例复发性/进展性GBM患者的临床资料。对客观缓解率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)、总生存期(OS)及治疗相关不良事件(AE)进行了回顾和评估。总ORR为52.6%,DCR为73.7%。中位PFS和OS分别为5.1个月和10.4个月。6个月的PFS率和OS率分别为38.9%和68.4%。12个月的PFS率和OS率分别为16.7%和36.8%。治疗相关毒性一般耐受性良好。最常见的3/4级AE为手足综合征(36.8%)和高血压(21.1%)。我们的研究表明,阿帕替尼治疗为复发性/进展性GBM患者提供了更好的挽救治疗选择,且毒性可控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b92b/9432461/f4403da8f5a8/fphar-13-969565-g001.jpg

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