Molecular imaging of solid tumors: exploiting the potential

被引:9
|
作者
Oyen, Wim J. G. [1 ]
van der Graaf, Winette T. A. [2 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Nucl Med, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Med Oncol, NL-6500 HB Nijmegen, Netherlands
关键词
POSITRON-EMISSION-TOMOGRAPHY; METASTATIC BREAST-CANCER; SQUAMOUS-CELL CARCINOMA; ESOPHAGOGASTRIC JUNCTION; PROGNOSTIC STRATIFICATION; F-18; FLUORODEOXYGLUCOSE; LUNG-CANCER; FDG-PET; CHEMOTHERAPY; EXPRESSION;
D O I
10.1038/nrclinonc.2009.139
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Targeted treatment has substantially changed the field of oncology. Compared with cytotoxic chemotherapy, many novel targeted therapies are administered over long periods of time, and result in disease stabilization rather than tumor shrinkage. The activity of these novel agents might, therefore, be better reflected by changes in molecular features of the tumor rather than reduction in size or volume. Thus, noninvasive procedures to measure such features are urgently needed. Factors that need to be predicted are early response (silencing of tumor signaling) or resistance to therapy, and whether therapy can be interrupted. Molecular imaging techniques, such as PET, may provide clinically relevant information; however, data are so far available mainly from small, observational, retrospective studies. Findings need to be further assessed in clinical trials to assess whether molecular imaging can be exploited and widely introduced to aid daily practice in oncology.
引用
收藏
页码:609 / 611
页数:3
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