Department of Endocrinology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands; Department of Medical Oncology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Department of Nuclear Medicine and Molecular Imaging, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Gastrointest Endosc. 2015 Jan;81(1):159-167.e2. doi: 10.1016/j.gie.2014.09.037.
In multiple endocrine neoplasia type 1 (MEN1), pancreatic neuroendocrine tumors (pNETs) are the leading MEN1-related cause of death.
To evaluate EUS and (11)C-5-hydroxytryptophan positron emission tomography ((11)C-5-HTP PET), compared with the recommended screening techniques in MEN1 patients for early detection of pNETs.
Cross-sectional study.
Tertiary-care university medical center.
This study involved 41 patients with a proven MEN1 mutation or with one MEN1 manifestation and a mutation carrier as a first-degree family member, with recent screening by abdominal CT or magnetic resonance imaging (MRI) and somatostatin receptor scintigraphy (SRS).
EUS by using a linear Pentax echoendoscope and Hitachi EUB-525 and (11)C-5-HTP PET.
Patient-based and lesion-based positivity for pNET was calculated for all imaging techniques. The McNemar test was used to compare the yield of the 4 imaging techniques.
In 35 of 41 patients, 107 pancreatic lesions were detected in total. EUS detected 101 pancreatic lesions in 34 patients, (11)C-5-HTP PET detected 35 lesions in 19 patients, and CT/MRI + SRS detected 32 lesions in 18 patients (P < .001). (11)C-5-HTP PET performed similarly to CT/MRI + SRS and better compared with SRS only (13 lesions in 12 patients), both at a patient-based and lesion-based level (P < .05).
Single-center study.
EUS is superior to CT/MRI + SRS for pancreatic lesion detection in patients with MEN1. In this setting, (11)C-5-HTP PET is not useful. We recommend EUS as the first-choice pancreas imaging technique in patients with MEN1. (
NTR1668.).
在多发性内分泌肿瘤 1 型(MEN1)中,胰腺神经内分泌肿瘤(pNET)是 MEN1 相关死亡的主要原因。
评估超声内镜(EUS)和 11C-5-羟色氨酸正电子发射断层扫描(11C-5-HTP PET),与 MEN1 患者的推荐筛查技术相比,用于早期检测 pNET。
横断面研究。
三级保健大学医学中心。
本研究涉及 41 例经证实的 MEN1 突变或具有 MEN1 表现且一级亲属为突变携带者的患者,最近进行了腹部 CT 或磁共振成像(MRI)和生长抑素受体闪烁显像(SRS)筛查。
使用线性 Pentax 超声内镜和日立 EUB-525 进行 EUS,并进行 11C-5-HTP PET。
计算所有影像学技术的 pNET 患者和病变阳性率。采用 McNemar 检验比较 4 种影像学技术的检出率。
在 41 例患者中,共检测到 107 个胰腺病变。EUS 在 34 例患者中检出 101 个胰腺病变,11C-5-HTP PET 在 19 例患者中检出 35 个病变,CT/MRI+SRS 在 18 例患者中检出 32 个病变(P<.001)。11C-5-HTP PET 的表现与 CT/MRI+SRS 相似,与仅 SRS 相比更好(12 例患者中有 13 个病变),在患者和病变层面均如此(P<.05)。
单中心研究。
EUS 优于 CT/MRI+SRS 检测 MEN1 患者的胰腺病变。在这种情况下,11C-5-HTP PET 没有用。我们建议 EUS 作为 MEN1 患者首选的胰腺成像技术。(临床试验注册号:NTR1668。)