为神经母细胞瘤患儿进行[18F]MFBG长轴视野PET/CT成像时无需镇静或全身麻醉。

Lise Borgwardt, Jesper Brok, Kim Francis Andersen, Jacob Madsen, Nicholas Gillings, Marie Øbro Fosbøl, Charlotte Lund Denholt, Ida Nymann Petersen, Louise Sørup Sørensen, Lotte Hahn Enevoldsen, Peter Sandor Oturai, Helle Hjort Johannesen, Liselotte Højgaard, Christina Schulze, Eunice Saxtoft, Flemming Andersen, Barbara Malene Fischer
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Replacing [<sup>123</sup>I]MIBG with the new PET tracer meta-[<sup>18</sup>F]fluorobenzylguanidine ([<sup>18</sup>F]MFBG) and further improving sensitivity and reducing noise in a new long-axial-field-of-view (LAFOV) PET/CT scanner enable increased image quality and a faster acquisition time, allowing examinations to be performed without sedation or general anesthesia (GA). Focusing on feasibility, we present our first experience with [<sup>18</sup>F]MFBG LAFOV PET/CT and compare it with [<sup>123</sup>I]MIBG scintigraphy plus SPECT/CT for imaging in neuroblastoma in children. <b>Methods:</b> A pilot of our prospective, single-center study recruited children with neuroblastoma who were referred for [<sup>123</sup>I]MIBG scintigraphy with SPECT/CT. Within 1 wk of [<sup>123</sup>I]MIBG scintigraphy and SPECT/low-dose CT, [<sup>18</sup>F]MFBG LAFOV PET/ultra-low-dose CT was performed 1 h after injection (1.5-3 MBq/kg) without sedation or GA, in contrast to the 24-h postinjection interval needed for scanning with [<sup>123</sup>I]MIBG, the 2- to 2.5-h acquisition time, and the GA often needed in children less than 6 y old. Based on the spirocyclic iodonium-ylide precursor, [<sup>18</sup>F]MFBG was produced in a fully automated good manufacturing practice-compliant procedure. We present the feasibility of the study. <b>Results:</b> In the first paired scans of the first 10 children included (5 at diagnosis, 2 during treatment, 2 during surveillance, and 1 at relapse), [<sup>18</sup>F]MFBG PET/CT scan showed a higher number of radiotracer-avid lesions in 80% of the cases and an equal number of lesions in 20% of the cases. The SIOPEN score was higher in 50% of the cases, and the Curie score was higher in 70% of the cases. 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引用次数: 0

摘要

元[123I]碘苄胍([123I]MIBG)闪烁扫描与 SPECT/CT 是诊断和监测神经母细胞瘤的标准疗法。用新型 PET 示踪剂元-[18F]氟苄胍([18F]MFBG)取代[123I]MIBG,并通过新型长轴视场(LAFOV)PET/CT 扫描仪进一步提高灵敏度和降低噪音,从而提高了图像质量并缩短了采集时间,使检查无需镇静或全身麻醉(GA)即可进行。我们以可行性为重点,介绍了我们首次使用[18F]MFBG LAFOV PET/CT 的经验,并将其与[123I]MIBG闪烁扫描加 SPECT/CT 用于儿童神经母细胞瘤成像的方法进行了比较。方法:我们的一项前瞻性单中心试验研究招募了神经母细胞瘤患儿,这些患儿被转诊接受[123I]MIBG闪烁显像加SPECT/CT检查。在[123I]MIBG闪烁扫描和SPECT/低剂量CT扫描后1周内,[18F]MFBG LAFOV PET/超低剂量CT在注射(1.5-3 MBq/kg)1小时后进行,无需镇静或GA,而[123I]MIBG扫描需要注射后24小时,采集时间为2-2.5小时,6岁以下儿童通常需要GA。[18F]MFBG以螺环碘化铵前体为基础,通过符合良好生产规范的全自动程序生产。我们介绍了这项研究的可行性。研究结果在首批纳入的 10 名儿童(5 名在诊断时、2 名在治疗期间、2 名在监测期间、1 名在复发时)的首次配对扫描中,[18F]MFBG PET/CT 扫描显示 80% 的病例有较多的放射性示踪剂拮抗病变,20% 的病例有相同数量的病变。50% 的病例 SIOPEN 评分较高,70% 的病例居里评分较高。尤其是椎管内、腹膜后淋巴结和骨髓受累的诊断精确度更高。所有患儿(中位年龄,1.6 岁;范围,0.1-7.9 岁)在 PET 过程中均未使用镇静剂或 GA,而 80% 的患儿在进行 SPECT/CT [123I]MIBG 闪烁扫描时使用了 GA。PET 采集时间仅为 2 分钟,且无运动伪影,这是在 10 分钟采集时间内进行重建以提供临床有用图像的数据要求。结论:这项试验性研究证明了[18F]MFBG LAFOV PET/CT 用于神经母细胞瘤成像的可行性。此外,与[123I]MIBG闪烁扫描和SPECT/CT相比,[18F]MFBG LAFOV PET/CT显示的放射性示踪剂拮抗病灶数量增加,SIOPEN评分增加,居里评分增加,而且所有患者都避免了GA和镇静剂。因此,[18F]MFBG LAFOV PET/CT采用1 d方案,扫描时间明显缩短,灵敏度更高,而且无需GA和镇静剂,有望用于未来的分期和反应评估,还可能对神经母细胞瘤患儿的治疗决策产生临床影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Performing [18F]MFBG Long-Axial-Field-of-View PET/CT Without Sedation or General Anesthesia for Imaging of Children with Neuroblastoma.

Meta-[123I]iodobenzylguanidine ([123I]MIBG) scintigraphy with SPECT/CT is the standard of care for diagnosing and monitoring neuroblastoma. Replacing [123I]MIBG with the new PET tracer meta-[18F]fluorobenzylguanidine ([18F]MFBG) and further improving sensitivity and reducing noise in a new long-axial-field-of-view (LAFOV) PET/CT scanner enable increased image quality and a faster acquisition time, allowing examinations to be performed without sedation or general anesthesia (GA). Focusing on feasibility, we present our first experience with [18F]MFBG LAFOV PET/CT and compare it with [123I]MIBG scintigraphy plus SPECT/CT for imaging in neuroblastoma in children. Methods: A pilot of our prospective, single-center study recruited children with neuroblastoma who were referred for [123I]MIBG scintigraphy with SPECT/CT. Within 1 wk of [123I]MIBG scintigraphy and SPECT/low-dose CT, [18F]MFBG LAFOV PET/ultra-low-dose CT was performed 1 h after injection (1.5-3 MBq/kg) without sedation or GA, in contrast to the 24-h postinjection interval needed for scanning with [123I]MIBG, the 2- to 2.5-h acquisition time, and the GA often needed in children less than 6 y old. Based on the spirocyclic iodonium-ylide precursor, [18F]MFBG was produced in a fully automated good manufacturing practice-compliant procedure. We present the feasibility of the study. Results: In the first paired scans of the first 10 children included (5 at diagnosis, 2 during treatment, 2 during surveillance, and 1 at relapse), [18F]MFBG PET/CT scan showed a higher number of radiotracer-avid lesions in 80% of the cases and an equal number of lesions in 20% of the cases. The SIOPEN score was higher in 50% of the cases, and the Curie score was higher in 70% of the cases. In particular, intraspinal, retroperitoneal lymph node, and bone marrow involvement was diagnosed with much higher precision. None of the children (median age, 1.6 y; range, 0.1-7.9 y) had sedation or GA during the PET procedure, whereas 80% had GA during [123I]MIBG scintigraphy with SPECT/CT. A PET acquisition time of only 2 min without motion artifacts was the data requirement of the 10-min acquisition time for reconstruction to provide a clinically useful image. Conclusion: This pilot study demonstrates the feasibility of performing [18F]MFBG LAFOV PET/CT for imaging of neuroblastoma. Further, an increased number of radiotracer-avid lesions, an increased SIOPEN score, and an increased Curie score were seen on [18F]MFBG LAFOV PET/CT compared with [123I]MIBG scintigraphy with SPECT/CT, and GA and sedation was avoided in all patients. Thus, with a 1-d protocol, a significantly shorter scan time, a higher sensitivity, and the avoidance of GA and sedation, [18F]MFBG LAFOV PET/CT shows promise for future staging and response assessment and may also have a clinical impact on therapeutic decision-making for children with neuroblastoma.

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