Malle Philipp, Sorschag Manfred, Gallowitsch Hans-Jürgen
Department of Nuclear Medicine and Endocrinology, PET-CT Center Klagenfurt, Klinikum Klagenfurt am Wörthersee, Feschnigstraße 11, 9020 Klagenfurt, Austria.
Wien Med Wochenschr. 2012 Oct;162(19-20):423-9. doi: 10.1007/s10354-012-0131-y. Epub 2012 Aug 14.
Gastrointestinal stromal tumours (GISTs) are fairly rare neoplasms, constituting less than 3 % of all gastrointestinal malignancies. The integration of molecularly targeted treatment regimes (i.e., tyrosine kinase inhibitors) in clinical oncology has revolutionized the management of patients with irresectable GISTs or metastatic disease. Malignant GISTs usually display increased glucose metabolism and therefore (18)F-fluorodeoxyglucose (FDG) uptake within the scope of positron emission tomography (PET) scans. Nowadays, dual-modality FDG PET/CT (computed tomography) imaging is of considerable value in diagnostic work-up of patients with GISTs acquiring functional and anatomic information simultaneously. The following article sheds light on the impact of FDG PET and combined FDG PET/CT imaging in initial disease evaluation, detection of tumour recurrence and the early assessment of treatment response to molecularly targeted agents such as imatinib mesylate or sunitinib maleate.
胃肠道间质瘤(GISTs)是相当罕见的肿瘤,占所有胃肠道恶性肿瘤的比例不到3%。分子靶向治疗方案(即酪氨酸激酶抑制剂)在临床肿瘤学中的整合彻底改变了不可切除GISTs或转移性疾病患者的治疗方式。恶性GISTs通常表现出葡萄糖代谢增加,因此在正电子发射断层扫描(PET)范围内(18)F-氟脱氧葡萄糖(FDG)摄取增加。如今,双模态FDG PET/CT(计算机断层扫描)成像在GISTs患者的诊断检查中具有重要价值,可同时获取功能和解剖信息。以下文章阐述了FDG PET及联合FDG PET/CT成像在初始疾病评估、肿瘤复发检测以及对甲磺酸伊马替尼或苹果酸舒尼替尼等分子靶向药物治疗反应的早期评估中的影响。