Henry Ford Health System, Hermelin Brain Tumor Center, 2799 W Grand Blvd, Detroit, MI 48202, USA.
J Neurooncol. 2010 Sep;99(2):237-42. doi: 10.1007/s11060-010-0121-0. Epub 2010 Feb 12.
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.
贝伐珠单抗治疗复发性高级别脑胶质瘤患者停药后,我们观察到肿瘤迅速复发或出现“反弹”的影像学现象,并伴有临床状况的加速恶化。我们回顾性分析了在亨利·福特·赫尔马林脑肿瘤中心接受治疗的 11 例复发性高级别脑胶质瘤患者,这些患者在停止使用贝伐珠单抗后表现出反弹进展模式。与反弹磁共振成像相比,原始肿瘤强化区平均增加了 158%。反弹后,没有患者(0/8)对不包括贝伐珠单抗的二线治疗有反应。再次接受贝伐珠单抗治疗的患者中位生存期为 149 天,而接受其他方案治疗的患者中位生存期为 32 天。肿瘤进展后贝伐珠单抗突然停药往往会导致明显的反弹现象和临床状况迅速恶化。肿瘤进展后逐渐减少贝伐珠单抗剂量可能会防止这种情况发生,并提高对二线治疗的反应性。