Advanced Solid Tumors Treated with Cediranib: Comparison of Dynamic Contrast-enhanced MR Imaging and CT as Markers of Vascular Activity

被引:42
作者
Messiou, Christina [1 ,2 ,4 ]
Orton, Matthew [1 ,2 ]
Ang, Joo Ern [3 ]
Collins, David J. [1 ,2 ]
Morgan, Veronica A. [1 ,2 ,4 ]
Mears, Dorothy [4 ]
Castellano, Isabel [4 ]
Papadatos-Pastos, Dionysis [3 ]
Brunetto, Andre [3 ]
Tunariu, Nina [1 ,2 ,4 ]
Mann, Helen [5 ]
Tessier, Jean [5 ]
Young, Helen [5 ]
Ghiorghiu, Dana [5 ]
Marley, Sarah [5 ]
Kaye, Stan B. [3 ]
deBono, Johann S. [3 ]
Leach, Martin O. [1 ,2 ]
deSouza, Nandita M. [1 ,2 ,4 ]
机构
[1] Inst Canc Res, Canc Res UK, Sutton SM2 5PT, Surrey, England
[2] Inst Canc Res, EPSRC Imaging Ctr, Sutton SM2 5PT, Surrey, England
[3] Inst Canc Res, Drug Dev Unit, Med Sect, Sutton SM2 5PT, Surrey, England
[4] Royal Marsden NHS Fdn Trust, Dept Radiol, Sutton, Surrey, England
[5] AstraZeneca, Macclesfield, Cheshire, England
基金
英国医学研究理事会; 英国工程与自然科学研究理事会;
关键词
QUANTITATIVE MEASUREMENTS; PERFUSION PARAMETERS; CLINICAL-TRIALS; LIVER-TUMORS; REPRODUCIBILITY; AZD2171; MODEL; AGREEMENT; CANCER; LUNG;
D O I
10.1148/radiol.12112565
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: To assess baseline reproducibility and compare performance of dynamic contrast material-enhanced (DCE) magnetic resonance (MR) imaging versus DCE computed tomographic (CT) measures of early vascular response in the same patients treated with cediranib (30 or 45 mg daily). Materials and Methods: After institutional review board approval, written informed consent was obtained from 29 patients with advanced solid tumors who had lesions 3 cm or larger and in whom simultaneous imaging of an adjacent artery was possible. Two baseline DCE MR acquisitions and two baseline DCE CT acquisitions 7 days or fewer apart (within 14 days of starting treatment) and two posttreatment acquisitions with each modality at day 7 and 28 (+/- 3 days) were obtained. Nonmodeled and modeled parameters were derived (measured arterial input function [AIF] for CT, population-based AIF for MR imaging; temporal sampling rate of 0.5 second for CT, 3-6 seconds for MR imaging). Baseline variability was assessed by using intra-and intersubject analysis of variance and Bland-Altman analysis; a paired t test assessed change from baseline to after treatment. Results: The most reproducible parameters were DCE MR imaging enhancement fraction (baseline intrapatient coefficient of variation [CV] = 8.6%), volume transfer constant (CV = 13.9%), and integrated area under the contrast uptake curve at 60 seconds (CV = 15.5%) and DCE CT positive enhancement integral (CV = 16.0%). Blood plasma volume was highly variable and the only parameter with CV greater than 30%. Average reductions (percentage change) from baseline were consistently observed for all DCE MR imaging and DCE CT parameters at day 7 and 28 for both starting-dose groups (45 and 30 mg), except for DCE CT mean transit time. Percentage change from baseline for parameters reflecting blood flow and permeability were comparable, and reductions from baseline at day 7 were maintained at day 28. Conclusion: DCE MR imaging and DCE CT can depict vascular response to antiangiogenic agents with response evident at day 7. Improved reproducibility with MR imaging favors its use in trials with small patient numbers.
引用
收藏
页码:426 / 436
页数:11
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