Young H, Baum R, Cremerius U, Herholz K, Hoekstra O, Lammertsma A A, Pruim J, Price P
MRC Cyclotron Unit, Imperial College School of Medicine, Hammersmith Hospital, London, U.K.
Eur J Cancer. 1999 Dec;35(13):1773-82. doi: 10.1016/s0959-8049(99)00229-4.
[18F]-fluorodeoxyglucose ([18F]-FDG) uptake is enhanced in most malignant tumours which in turn can be measured using positron emission tomography (PET). A number of small clinical trials have indicated that quantification of the change in tumour [18F]-FDG uptake may provide an early, sensitive, pharmacodynamic marker of the tumoricidal effect of anticancer drugs. This may allow for the introduction of subclinical response for anticancer drug evaluation in early clinical trials and improvements in patient management. For comparison of results from smaller clinical trials and larger-scale multicentre trials a consensus is desirable for: (i) common measurement criteria; and (ii) reporting of alterations in [18F]-FDG uptake with treatment. This paper summarises the current status of the technique and recommendations on the measurement of [18F]-FDG uptake for tumour response monitoring from a consensus meeting of the European Organization for Research and Treatment of Cancer (EORTC) PET study group held in Brussels in February 1998 and confirmed at a subsequent meeting in March 1999.
大多数恶性肿瘤中[18F] - 氟脱氧葡萄糖([18F] - FDG)摄取增强,进而可使用正电子发射断层扫描(PET)进行测量。一些小型临床试验表明,肿瘤[18F] - FDG摄取变化的量化可能为抗癌药物的杀瘤作用提供早期、敏感的药效学标志物。这可能使得在早期临床试验中引入亚临床反应以评估抗癌药物,并改善患者管理。为了比较小型临床试验和大规模多中心试验的结果,对于以下方面达成共识是可取的:(i)通用测量标准;以及(ii)报告治疗过程中[18F] - FDG摄取的变化。本文总结了该技术的现状以及关于[18F] - FDG摄取测量用于肿瘤反应监测的建议,这些建议来自1998年2月在布鲁塞尔举行的欧洲癌症研究与治疗组织(EORTC)PET研究组共识会议,并在1999年3月的后续会议上得到确认。