Apparent diffusion coefficient from magnetic resonance imaging as a biomarker in oncology drug development

被引:59
|
作者
Sinkus, Ralph [1 ]
Van Beers, Bernard E. [1 ]
Vilgrain, Valerie [1 ]
DeSouza, Nandita [2 ,3 ]
Waterton, John C. [4 ]
机构
[1] Beaujon Hosp, INSERM, U773, Ctr Rech Biomed Bichat Beaujon CRB3, Clichy, France
[2] Inst Canc Res, Sutton SM2 5PT, Surrey, England
[3] Royal Marsden Hosp, Sutton SM2 5PT, Surrey, England
[4] AstraZeneca Personalised Healthcare & Biomarkers, Macclesfield SK10 4TG, Cheshire, England
关键词
Diffusion weighted MRI; ADC; Cell membrane integrity; Tumor response; VASCULAR TARGETING AGENT; FOCAL LIVER-LESIONS; ADC MEASUREMENTS; TUMOR RESPONSE; BREAST-CANCER; NECK-CANCER; CELLULARITY; FIBROSIS; MRI; FEASIBILITY;
D O I
10.1016/j.ejca.2011.11.034
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Magnetic resonance imaging (MRI) can be made sensitive to diffusion of water molecules in biological tissues: this phenomenon can be quantitated to provide a biomarker, the apparent diffusion coefficient (ADC). Over the past decade, evidence has accumulated from numerous clinical and animal studies that ADC is abnormal in tumours; that elevated ADC reflects an elevated non-cellular fraction; and that acute increases in ADC following therapy can indicate that tumour cells have been killed. However there remain substantial challenges in ensuring robust and valid ADC measurements, particularly in multicentre studies in common sites of metastasis such as lung and liver. Moreover, there is uncertainty about how best to select the timing of observation post-therapy to avoid false-negatives, and how to minimise the confounding factors which could decouple drug-induced ADC increase from drug-induced cell kill. In this review we summarise the physical basis of the biomarker, the evidence that it reflects non-viable fraction, particularly in extracranial tumours, and suggest a roadmap for validation and qualification. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:425 / 431
页数:7
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