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

被引:66
作者
Zuniga, Richard M. [1 ]
Torcuator, Roy [1 ,2 ]
Jain, Rajan [3 ]
Anderson, John [4 ]
Doyle, Thomas [4 ]
Schultz, Lonni [5 ]
Mikkelsen, Tom [1 ,2 ]
机构
[1] Henry Ford Hlth Syst, Hermelin Brain Tumor Ctr, Detroit, MI 48202 USA
[2] Henry Ford Hlth Syst, Dept Neurosurg, Detroit, MI USA
[3] Henry Ford Hlth Syst, Dept Neuroradiol, Detroit, MI USA
[4] Henry Ford Hlth Syst, Dept Med Oncol, Detroit, MI USA
[5] Henry Ford Hlth Syst, Dept Biostat & Res Epidemiol, Detroit, MI USA
关键词
Glioma; Bevacizumab; Rebound; Recurrent glioma; Glioblastoma; PHASE-II; MALIGNANT GLIOMAS; PACLITAXEL; IRINOTECAN; EFFICACY; PATTERNS; TRIAL; VEGF;
D O I
10.1007/s11060-010-0121-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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.
引用
收藏
页码:237 / 242
页数:6
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