Krause B J, Schwarzenböck S, Schwaiger M
Klinik und Poliklinik für Nuklearmedizin, Klinikum rechts der Isar, Technische Universität München, Ismaninger Str, 22, 81675 München.
Nuklearmedizin. 2010;49 Suppl 1:S41-5.
In oncology, PET and PET/CT with tracers beyond FDG target more specific biological processes, such as proliferation (18F-3´-fluoro-3´-deoxy-L-thymidine; 18F-FLT), tumour hypoxia (18F-fluoromisonidazol; 18F-FMISO) and phospholipid metabolism (radioactively labelled choline derivates). FLT is a thymidine analogue which can be labelled with 18F. PET with 18F-FLT enables to non-invasively image and to quantify the proliferation fraction of tumours. Proliferation dependent accumulation of FLT has been demonstrated for a variety of solid and haematologic neoplasms including lung cancer, breast cancer, gastric cancer, colorectal cancer and malignant lymphoma. Furthermore, FLT has been suggested as surrogate marker for the assessment of response to treatment, especially when targeted drugs are utilized. PET imaging in particular has emerged as a promising non-invasive tool to accurately characterize tumour oxygenation. The great promise of PET/CT is its potential as a single imaging modality for whole body staging that provides anatomical and biological information on the disease as a whole. It allows a more precise estimation of the hypoxic tumour volume as well as comparisons on a voxel-by-voxel basis (parametric mapping). PET and PET/CT with hypoxia tracers thus offer the potential to optimize and individualize therapy for patients suffering from cancer. PET- and PET/CT-studies using 11C- or 18F-labeled choline derivates recently have shown promising results for re-staging prostate cancer in patients with biochemical recurrence and advanced prostate cancer. In patients with biochemical recurrence of prostate cancer after primary therapy the detection rate of 11C-choline-PET/CT shows a positive relationship with serum PSA-levels. In these patients 11C-choline PET/CT allows not only to diagnose but also to localize recurrent disease with implications on disease management (localised vs. systemic therapy).
The clinical success of multimodal imaging with PET/CT is expected to promote the combination of MRI and PET in the future.
在肿瘤学中,使用除氟代脱氧葡萄糖(FDG)之外的示踪剂的正电子发射断层扫描(PET)和PET/计算机断层扫描(CT)针对更特定的生物学过程,如增殖(18F-3'-氟-3'-脱氧-L-胸腺嘧啶核苷;18F-FLT)、肿瘤缺氧(18F-氟米索硝唑;18F-FMISO)和磷脂代谢(放射性标记的胆碱衍生物)。FLT是一种胸腺嘧啶类似物,可用18F进行标记。使用18F-FLT的PET能够对肿瘤的增殖分数进行无创成像和定量。已证实多种实体瘤和血液系统肿瘤(包括肺癌、乳腺癌、胃癌、结直肠癌和恶性淋巴瘤)中存在FLT依赖增殖的聚集。此外,FLT已被建议作为评估治疗反应的替代标志物,尤其是在使用靶向药物时。PET成像尤其已成为一种有前景的无创工具,可准确表征肿瘤氧合情况。PET/CT的巨大前景在于其作为一种单一成像模式用于全身分期的潜力,它能提供关于整个疾病的解剖学和生物学信息。它能更精确地估计缺氧肿瘤体积,并进行逐体素比较(参数映射)。因此,使用缺氧示踪剂的PET和PET/CT为优化和个体化癌症患者的治疗提供了潜力。最近使用11C或18F标记的胆碱衍生物进行的PET和PET/CT研究在对生化复发和晚期前列腺癌患者进行前列腺癌再分期方面显示出有前景的结果。在接受初始治疗后出现前列腺癌生化复发的患者中,11C-胆碱-PET/CT的检出率与血清前列腺特异性抗原(PSA)水平呈正相关。在这些患者中,11C-胆碱PET/CT不仅能诊断复发性疾病,还能对其进行定位,这对疾病管理(局部治疗与全身治疗)有影响。
PET/CT多模态成像的临床成功有望在未来推动磁共振成像(MRI)和PET的联合应用。