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18F-FDG硅光电倍增管PET/CT:一项将半定量测量与标准PET/CT进行比较的初步研究。

18F-FDG silicon photomultiplier PET/CT: A pilot study comparing semi-quantitative measurements with standard PET/CT.

作者信息

Baratto Lucia, Park Sonya Young, Hatami Negin, Davidzon Guido, Srinivas Shyam, Gambhir Sanjiv Sam, Iagaru Andrei

机构信息

Division of Nuclear Medicine and Molecular Imaging, Stanford University Medical Center, Stanford, California, United States of America.

Radiological Sciences Laboratory, Stanford University, Stanford, California, United States of America.

出版信息

PLoS One. 2017 Jun 5;12(6):e0178936. doi: 10.1371/journal.pone.0178936. eCollection 2017.

Abstract

PURPOSE

To evaluate if the new Discovery Molecular Insights (DMI) PET/CT scanner provides equivalent results compared to the standard of care PET/CT scanners (GE Discovery 600 or GE Discovery 690) used in our clinic and to explore any possible differences in semi-quantitative measurements.

METHODS

The local Institutional Review Board approved the protocol and written informed consent was obtained from each patient. Between September and November 2016, 50 patients underwent a single 18F-FDG injection and two scans: the clinical standard PET/CT followed immediately by the DMI PET/CT scan. We measured SUVmax and SUVmean of different background organs and up to four lesions per patient from data acquired using both scanners.

RESULTS

DMI PET/CT identified all the 107 lesions detected by standard PET/CT scanners, as well as additional 37 areas of focal increased 18F-FDG uptake. The SUVmax values for all 107 lesions ranged 1.2 to 14.6 (mean ± SD: 2.8 ± 2.8), higher on DMI PET/CT compared with standard of care PET/CT. The mean lesion:aortic arch SUVmax ratio and mean lesion:liver SUVmax ratio were 0.2-15.2 (mean ± SD: 3.2 ± 2.6) and 0.2-8.5 (mean ± SD: 1.9 ± 1.4) respectively, higher on DMI PET/CT than standard PET/CT. These differences were statistically significant (P value < 0.0001) and not correlated to the delay in acquisition of DMI PET data (P < 0.0001).

CONCLUSIONS

Our study shows high performance of the new DMI PET/CT scanner. This may have a significant role in diagnosing and staging disease, as well as for assessing and monitoring responses to therapies.

摘要

目的

评估新型Discovery Molecular Insights(DMI)PET/CT扫描仪与我们诊所使用的标准护理PET/CT扫描仪(GE Discovery 600或GE Discovery 690)相比是否能提供等效结果,并探讨半定量测量中任何可能存在的差异。

方法

当地机构审查委员会批准了该方案,并获得了每位患者的书面知情同意书。在2016年9月至11月期间,50名患者接受了单次18F-FDG注射和两次扫描:先进行临床标准PET/CT扫描,随后立即进行DMI PET/CT扫描。我们从两台扫描仪获取的数据中测量了不同背景器官的SUVmax和SUVmean,以及每位患者多达四个病灶的相关数据。

结果

DMI PET/CT识别出了标准PET/CT扫描仪检测到的所有107个病灶,以及另外37个18F-FDG摄取局灶性增加的区域。所有107个病灶的SUVmax值范围为1.2至14.6(平均值±标准差:2.8±2.8),DMI PET/CT上的值高于标准护理PET/CT。平均病灶:主动脉弓SUVmax比值和平均病灶:肝脏SUVmax比值分别为0.2至15.2(平均值±标准差:3.2±2.6)和0.2至8.5(平均值±标准差:1.9±1.4),DMI PET/CT上的值高于标准PET/CT。这些差异具有统计学意义(P值<0.0001),且与DMI PET数据采集延迟无关(P<0.0001)。

结论

我们的研究表明新型DMI PET/CT扫描仪具有高性能。这在疾病的诊断和分期以及评估和监测治疗反应方面可能具有重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f41/5459477/900f5f31135e/pone.0178936.g001.jpg

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