Department of Neurosurgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Department of Radiation Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Cancer Med. 2019 Nov;8(15):6519-6527. doi: 10.1002/cam4.2537. Epub 2019 Sep 9.
Bevacizumab improves symptoms via reducing the peritumoral edema and/or normalizing blood brain barrier, and occasionally via reducing the tumor size. However, the effect against active cystic components has not been documented yet.
Between 2008 and 2018, 139 patients with primary or metastatic brain tumors were treated with bevacizumab (BEV) in our institution. The images and symptoms before and after administration of BEV were examined, and changes in size of cysts were evaluated as follows: CR (complete disappearance), PR (reduction by ≥50%), MR (reduction by ≥25%), SD (size change <25%), PD (increase by ≥25%). The effect of BEV on tumor itself was determined according to Response Assessment in Neuro-Oncology criteria.
Of the 139 patients, 21 (15.1%) had cystic components. The best responses of cysts to BEV treatment were as follows: CR 6, PR 7, MR 4, SD 4. The group of patients with progressively increasing cysts prior to BEV treatment had significant cyst size reduction compared to stable cyst size groups, at initial imaging after BEV (mean 62.6% vs 22.5%, P = .0055) and at best response timing (mean 76.3% vs 32.8%, P = .0050). Patients with cysts showed significant improvement in symptoms after the treatment with BEV compared to patients without cysts (P = .0033). However, response rate was not different between patients with or without cysts. Overall survival after starting BEV was not different between glioblastoma patients with or without cysts.
Bevacizumab is effective against progressively increasing cysts. Although cysts reduction effect and tumor response and/or overall survival are independent, BEV may be effective in patients who are symptomatic due to cyst enlargement.
贝伐单抗通过减少瘤周水肿和/或使血脑屏障正常化,偶尔通过缩小肿瘤体积来改善症状。然而,其对活跃性囊性成分的作用尚未得到证实。
在 2008 年至 2018 年间,我院对 139 例原发性或转移性脑肿瘤患者使用贝伐单抗(bevacizumab,BEV)治疗。检查了患者接受 BEV 治疗前后的图像和症状,并评估了囊肿大小的变化情况:完全消失(CR)、减少≥50%(PR)、减少≥25%(MR)、变化<25%(SD)、增加≥25%(PD)。根据神经肿瘤学反应评估标准确定 BEV 对肿瘤本身的影响。
在 139 例患者中,21 例(15.1%)有囊性成分。囊性成分对 BEV 治疗的最佳反应如下:CR 6 例,PR 7 例,MR 4 例,SD 4 例。与囊性成分稳定的患者相比,在 BEV 治疗前囊性成分持续增大的患者在接受 BEV 初始影像学检查时(平均 62.6%比 22.5%,P=0.0055)和最佳反应时(平均 76.3%比 32.8%,P=0.0050)的囊性成分体积有显著减小。与无囊性成分的患者相比,接受 BEV 治疗后有囊性成分的患者症状有显著改善(P=0.0033)。然而,有囊性成分和无囊性成分的患者的反应率没有差异。开始使用 BEV 后,胶质母细胞瘤患者的总体生存率与有无囊性成分之间没有差异。
贝伐单抗对持续增大的囊肿有效。虽然囊肿缩小的效果、肿瘤的反应和/或总体生存率是独立的,但对于因囊肿增大而出现症状的患者,BEV 可能是有效的。