Molecular imaging in cancer treatment

被引:70
作者
Michalski, Mark H. [2 ]
Chen, Xiaoyuan [1 ]
机构
[1] NIBIB, Lab Mol Imaging & Nanomed LOMIN, NIH, Bethesda, MD 20892 USA
[2] Stanford Univ, Sch Med, Stanford, CA 94305 USA
关键词
Molecular imaging; Therapy response; Metabolism; Proliferation; Angiogenesis; Hypoxia; Apoptosis; POSITRON-EMISSION-TOMOGRAPHY; ENDOTHELIAL GROWTH-FACTOR; CELL LUNG-CANCER; MATRIX-METALLOPROTEINASE INHIBITORS; INTEGRIN ALPHA(V)BETA(3) EXPRESSION; HYPOXIC TISSUE TRACER; IN-VIVO DETECTION; BREAST-CANCER; TUMOR HYPOXIA; F-18-FDG PET;
D O I
10.1007/s00259-010-1569-z
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
The success of cancer therapy can be difficult to predict, as its efficacy is often predicated upon characteristics of the cancer, treatment, and individual that are not fully understood or are difficult to ascertain. Monitoring the response of disease to treatment is therefore essential and has traditionally been characterized by changes in tumor volume. However, in many instances, this singular measure is insufficient for predicting treatment effects on patient survival. Molecular imaging allows repeated in vivo measurement of many critical molecular features of neoplasm, such as metabolism, proliferation, angiogenesis, hypoxia, and apoptosis, which can be employed for monitoring therapeutic response. In this review, we examine the current methods for evaluating response to treatment and provide an overview of emerging PET molecular imaging methods that will help guide future cancer therapies.
引用
收藏
页码:358 / 377
页数:20
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