Vanderbilt University Institute of Imaging Science, Vanderbilt University, 1161 21st Ave. S., AA1105 MCN, Nashville, TN 37232-2310, USA.
Ann Nucl Med. 2012 Nov;26(9):757-63. doi: 10.1007/s12149-012-0636-x. Epub 2012 Jul 22.
Molecular imaging biomarkers of proliferation hold great promise for quantifying response to personalized medicine. One such approach utilizes the positron emission tomography (PET) tracer 3'-deoxy-3'[18F]-fluorothymidine ([18F]FLT), an investigational agent whose uptake reflects thymidine salvage-dependent DNA synthesis. The goal of this study was to evaluate [18F]FLT-PET in the setting of Ménétrier's disease (MD), a rare, premalignant hyperproliferative disorder of the stomach treatable with cetuximab therapy. Over 15 months, a patient with confirmed MD underwent cetuximab therapy and was followed with sequential [18F]FLT-PET. For comparison to MD, an [18F]FLT-PET study was conducted in another patient to quantify uptake in a normal stomach. Prior to cetuximab therapy, stomach tissue in MD was easily visualized with [18F]FLT-PET, with pre-treatment uptake levels exceeding normal stomach uptake by approximately fourfold. Diminished [18F]FLT-PET in MD was observed following the initial and subsequent doses of cetuximab and correlated with clinical resolution of the disease. To our knowledge, this study reports the first clinical use of [18F]FLT-PET to assess proliferation in a premalignant disorder. We illustrate that the extent of MD involvement throughout the stomach could be easily visualized using [18F]FLT-PET, and that response to cetuximab could be followed quantitatively and non-invasively in sequential [18F]FLT-PET studies. Thus, [18F]FLT-PET appears to have potential to monitor response to treatment in this and potentially other hyperproliferative disorders.
分子影像学增殖标志物在定量评估个体化医学的反应方面具有很大的潜力。其中一种方法是利用正电子发射断层扫描(PET)示踪剂 3'-去氧-3'[18F]-氟胸苷([18F]FLT),这是一种研究性药物,其摄取反映了胸苷补救依赖的 DNA 合成。本研究的目的是评估[18F]FLT-PET 在 Menetrier 病(MD)中的应用,MD 是一种罕见的、具有潜在恶性的胃高增殖性疾病,可用西妥昔单抗治疗。在 15 个月的时间里,一名确诊为 MD 的患者接受了西妥昔单抗治疗,并进行了连续的[18F]FLT-PET 检查。为了与 MD 进行比较,对另一名患者进行了[18F]FLT-PET 检查,以定量测量正常胃中的摄取。在接受西妥昔单抗治疗之前,MD 胃组织很容易通过[18F]FLT-PET 进行可视化,治疗前的摄取水平比正常胃摄取水平高出约四倍。在用西妥昔单抗治疗初始和后续剂量后,MD 中的[18F]FLT-PET 减少,并与疾病的临床缓解相关。据我们所知,本研究首次报告了[18F]FLT-PET 用于评估癌前病变增殖的临床应用。我们表明,[18F]FLT-PET 可以很容易地显示整个胃 MD 的受累程度,并且可以通过连续的[18F]FLT-PET 研究定量和非侵入性地监测对西妥昔单抗的反应。因此,[18F]FLT-PET 似乎有可能监测这种和其他潜在的高增殖性疾病对治疗的反应。