Schmainda Kathleen M, Zhang Zheng, Prah Melissa, Snyder Bradley S, Gilbert Mark R, Sorensen A Gregory, Barboriak Daniel P, Boxerman Jerrold L
Department of Radiology, Medical College of Wisconsin, Milwaukee, Wisconsin (K.M.S., M.P.); Department of Biostatistics and Center for Statistical Sciences, Brown University, Providence, Rhode Island (Z.Z., B.S.S.); Department of Neuro-Oncology, University of Texas M.D. Anderson Cancer Center, Houston, Texas (M.R.G.); Department of Radiology, Massachusetts General Hospital, Charlestown, Massachusetts (A.G.S.); Department of Radiology, Duke University Medical Center, Durham, North Carolina (D.P.B.); Department of Diagnostic Imaging, Rhode Island Hospital, Providence, Rhode Island (J.L.B.); Alpert Medical School of Brown University, Providence, Rhode Island (J.L.B.).
Neuro Oncol. 2015 Aug;17(8):1148-56. doi: 10.1093/neuonc/nou364. Epub 2015 Feb 2.
The study goal was to determine whether changes in relative cerebral blood volume (rCBV) derived from dynamic susceptibility contrast (DSC) MRI are predictive of overall survival (OS) in patients with recurrent glioblastoma multiforme (GBM) when measured 2, 8, and 16 weeks after treatment initiation.
Patients with recurrent GBM (37/123) enrolled in ACRIN 6677/RTOG 0625, a multicenter, randomized, phase II trial of bevacizumab with irinotecan or temozolomide, consented to DSC-MRI plus conventional MRI, 21 with DSC-MRI at baseline and at least 1 postbaseline scan. Contrast-enhancing regions of interest were determined semi-automatically using pre- and postcontrast T1-weighted images. Mean tumor rCBV normalized to white matter (nRCBV) and standardized rCBV (sRCBV) were determined for these regions of interest. The OS rates for patients with positive versus negative changes from baseline in nRCBV and sRCBV were compared using Wilcoxon rank-sum and Kaplan-Meier survival estimates with log-rank tests.
Patients surviving at least 1 year (OS-1) had significantly larger decreases in nRCBV at week 2 (P = .0451) and sRCBV at week 16 (P = .014). Receiver operating characteristic analysis found the percent changes of nRCBV and sRCBV at week 2 and sRCBV at week 16, but not rCBV data at week 8, to be good prognostic markers for OS-1. Patients with positive change from baseline rCBV had significantly shorter OS than those with negative change at both week 2 and week 16 (P = .0015 and P = .0067 for nRCBV and P = .0251 and P = .0004 for sRCBV, respectively).
Early decreases in rCBV are predictive of improved survival in patients with recurrent GBM treated with bevacizumab.
本研究的目的是确定在开始治疗2周、8周和16周时,通过动态磁敏感对比(DSC)磁共振成像(MRI)获得的相对脑血容量(rCBV)变化是否可预测复发性多形性胶质母细胞瘤(GBM)患者的总生存期(OS)。
参加ACRIN 6677/RTOG 0625(一项贝伐单抗联合伊立替康或替莫唑胺的多中心、随机、II期试验)的复发性GBM患者(37/123)同意接受DSC-MRI加传统MRI检查,其中21例在基线时及至少1次基线后扫描时接受DSC-MRI检查。使用对比剂前和对比剂后T1加权图像半自动确定感兴趣的强化区域。对这些感兴趣区域测定平均肿瘤rCBV相对于白质的标准化值(nRCBV)和标准化rCBV(sRCBV)。使用Wilcoxon秩和检验以及带有对数秩检验的Kaplan-Meier生存估计法比较nRCBV和sRCBV相对于基线变化为阳性和阴性的患者的OS率。
存活至少1年(OS-1)的患者在第2周时nRCBV显著下降(P = 0.0451),在第16周时sRCBV显著下降(P = 0.014)。受试者工作特征分析发现,第2周时nRCBV和sRCBV的百分比变化以及第16周时sRCBV的百分比变化是OS-1的良好预后标志物,但第8周时的rCBV数据不是。在第2周和第16周时,相对于基线rCBV变化为阳性的患者的OS显著短于变化为阴性的患者(nRCBV分别为P = 0.0015和P = 0.0067,sRCBV分别为P = 0.0251和P = 0.0004)。
rCBV早期下降可预测接受贝伐单抗治疗的复发性GBM患者生存期改善。