首页> 外文期刊>Journal of neuro-oncology. >Rebound tumour progression after the cessation of bevacizumab therapy in patients with recurrent high-grade glioma.
【24h】

Rebound tumour progression after the cessation of bevacizumab therapy in patients with recurrent high-grade glioma.

机译:复发性高级别神经胶质瘤患者停止贝伐单抗治疗后的反弹性肿瘤进展。

获取原文
获取原文并翻译 | 示例
           

摘要

After withdrawal of bevacizumab in patients with recurrent high-grade glioma, we have observed a rapid tumour re-growth or "rebound" radiographic phenomenon with accelerated clinical decline. We retrospectively reviewed 11 patients treated at the Henry Ford Hermelin Brain Tumor Center with recurrent high-grade glioma who demonstrated a rebound progression pattern after the discontinuation of bevacizumab. The original tumour area-of-enhancement increased by a mean of 158%, when compared to the rebound magnetic resonance imaging. After rebound, no patients (0/8) showed a response to next-line treatments that did not include bevacizumab. The median survival of those re-treated with bevacizumab was 149 and 32 days for those who received other regimens. Abrupt discontinuation of bevacizumab after recurrence often leads to a dramatic rebound phenomenon and rapid clinical decline. Slow tapering of the bevacizumab dose after tumour progression may prevent this from occurring and improve responsiveness to next-line therapies.
机译:在患有复发性高级别神经胶质瘤的患者中停用贝伐单抗后,我们观察到了快速的肿瘤重新生长或“反弹”影像学现象,并加速了临床衰退。我们回顾性分析了在亨利·福特·赫梅林脑肿瘤中心接受治疗的11例复发性高级别神经胶质瘤患者,这些患者在停用贝伐单抗后表现出反弹进程。与反弹磁共振成像相比,原始肿瘤增强区域平均增加了158%。反弹后,没有患者(0/8)对不包括贝伐单抗的下一线治疗有反应。对于接受其他方案的患者,用贝伐单抗复治的患者的中位生存期为149天和32天。复发后贝伐单抗的突然停药通常会导致剧烈的反弹现象和快速的临床下降。肿瘤进展后贝伐单抗剂量的逐渐减量可防止这种情况的发生并改善对下一线疗法的反应性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号