Promise and pitfalls of quantitative imaging in oncology clinical trials

被引:77
作者
Kurland, Brenda F. [1 ]
Gerstner, Elizabeth R. [2 ]
Mountz, James M. [3 ]
Schwartz, Lawrence H. [4 ]
Ryan, Christopher W. [5 ]
Graham, Michael M. [6 ]
Buatti, John M. [6 ]
Fennessy, Fiona M. [7 ]
Eikman, Edward A. [8 ]
Kumar, Virendra [8 ]
Forster, Kenneth M. [8 ]
Wahl, Richard L. [9 ]
Lieberman, Frank S. [3 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Seattle, WA 98019 USA
[2] Massachusetts Gen Hosp, Boston, MA 02114 USA
[3] Univ Pittsburgh, Pittsburgh, PA USA
[4] Columbia Univ, New York, NY USA
[5] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[6] Univ Iowa, Iowa City, IA USA
[7] Brigham & Womens Hosp, Boston, MA 02115 USA
[8] Univ S Florida, H Lee Moffitt Canc Ctr, Tampa, FL 33682 USA
[9] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
MRI; CT; PET; Quantitative imaging; Clinical trials; Cancer; POSITRON-EMISSION-TOMOGRAPHY; APPARENT DIFFUSION-COEFFICIENT; GASTROINTESTINAL STROMAL TUMOR; STANDARDIZED UPTAKE VALUES; LOCALIZED PROSTATE-CANCER; ADVANCED BREAST-CANCER; CELL LUNG-CANCER; F-18-FDG PET; PHASE-II; NEOADJUVANT CHEMOTHERAPY;
D O I
10.1016/j.mri.2012.06.009
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
Quantitative imaging using computed tomography, magnetic resonance imaging and positron emission tomography modalities will play an increasingly important role in the design of oncology trials addressing molecularly targeted, personalized therapies. The advent of molecularly targeted therapies, exemplified by antiangiogenic drugs, creates new complexities in the assessment of response. The Quantitative Imaging Network addresses the need for imaging modalities which can accurately and reproducibly measure not just change in tumor size but changes in relevant metabolic parameters, modulation of relevant signaling pathways, drug delivery to tumor and differentiation of apoptotic cell death from other changes in tumor volume. This article provides an overview of the applications of quantitative imaging to phase 0 through phase 3 oncology trials. We describe the use of a range of quantitative imaging modalities in specific tumor types including malignant gliomas, lung cancer, head and neck cancer, lymphoma, breast cancer, prostate cancer and sarcoma. In the concluding section, we discuss potential constraints on clinical trials using quantitative imaging, including complexity of trial conduct, impact on subject recruitment, incremental costs and institutional barriers. Strategies for overcoming these constraints are presented. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:1301 / 1312
页数:12
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