Mankoff David A, Shields Anthony F, Krohn Kenneth A
Division of Nuclear Medicine, Department of Radiology, University of Washington, 1959 Northeast Pacific Street, Room NN203, Box 356113, Seattle, WA 98195, USA.
Radiol Clin North Am. 2005 Jan;43(1):153-67. doi: 10.1016/j.rcl.2004.09.005.
PET cellular proliferation imaging has its roots in a long history of in vitro cellular proliferation studies to characterize cancer and in the understanding of the biology of thymidine incorporation into DNA gained from these studies. PET imaging represents the logical translation of the in vitro work to measure in vivo tumor proliferation. Preclinical studies of [11C]-thymidine and other PET-labeled thymidine analogues set the stage for early clinical studies that provided very promising results. Recent progress in the application of [18F]-FLT, a clinically practical PET thymidine analogue, to patient studies sets the next stage for clinical PET cellular proliferation imaging. Further mechanistic studies of the imaging agents and well-designed clinical trials will be important in moving PET proliferation imaging into what is likely to be a significant role in the care of cancer patients by providing a quantitative measure of tumor response to cytotoxic or cytostatic therapy.
正电子发射断层扫描(PET)细胞增殖成像源于长期的体外细胞增殖研究,旨在表征癌症,并源于对这些研究中获得的胸苷掺入DNA生物学过程的理解。PET成像代表了将体外研究成果合理转化为体内肿瘤增殖的测量方法。[11C] -胸苷和其他PET标记的胸苷类似物的临床前研究为早期临床研究奠定了基础,这些早期临床研究取得了非常有前景的结果。[18F] -氟代胸苷([18F]-FLT)作为一种临床实用的PET胸苷类似物,在患者研究中的最新应用为临床PET细胞增殖成像的下一阶段发展奠定了基础。对成像剂进行进一步的机制研究以及精心设计的临床试验,对于推动PET增殖成像在癌症患者护理中发挥重要作用至关重要,因为它可以提供肿瘤对细胞毒性或细胞抑制疗法反应的定量测量。