如何从 89Zr-immuno-PET 扫描图像中获取血液浓度。

IF 3 2区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING EJNMMI Physics Pub Date : 2024-02-07 DOI:10.1186/s40658-024-00621-7
Jessica E Wijngaarden, Amina Ahbari, Johanna E E Pouw, Henri N J M Greuter, Idris Bahce, Gerben J C Zwezerijnen, Daniëlle J Vugts, Guus A M S van Dongen, Ronald Boellaard, C Willemien Menke-van der Houven van Oordt, Marc C Huisman
{"title":"如何从 89Zr-immuno-PET 扫描图像中获取血液浓度。","authors":"Jessica E Wijngaarden, Amina Ahbari, Johanna E E Pouw, Henri N J M Greuter, Idris Bahce, Gerben J C Zwezerijnen, Daniëlle J Vugts, Guus A M S van Dongen, Ronald Boellaard, C Willemien Menke-van der Houven van Oordt, Marc C Huisman","doi":"10.1186/s40658-024-00621-7","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>PET scans using zirconium-89 labelled monoclonal antibodies (<sup>89</sup>Zr-mAbs), known as <sup>89</sup>Zr-immuno-PET, are made to measure uptake in tumour and organ tissue. Uptake is related to the supply of <sup>89</sup>Zr-mAbs in the blood. Measuring activity concentrations in blood, however, requires invasive blood sampling. This study aims to identify the best delineation strategy to obtain the image-derived blood concentration (IDBC) from <sup>89</sup>Zr-immuno-PET scans.</p><p><strong>Methods: </strong>PET imaging and blood sampling of two <sup>89</sup>Zr-mAbs were included, <sup>89</sup>Zr-cetuximab and <sup>89</sup>Zr-durvalumab. For seven patients receiving <sup>89</sup>Zr-cetuximab, PET scans on 1-2 h, 2 and 6 days post-injection (p.i.) were analysed. Five patients received three injections of <sup>89</sup>Zr-durvalumab. The scanning protocol for the first two injections consisted of PET scanning on 2, 5 and 7 days p.i. and for the third injection only on 7 days p.i. Blood samples were drawn with every PET scan and the sample-derived blood concentration (SDBC) was used as gold standard for the IDBC. According to an in-house developed standard operating procedure, the aortic arch, ascending aorta, descending aorta and left ventricle were delineated. Bland-Altman analyses were performed to assess the bias (mean difference) and variability (1.96 times the standard deviation of the differences) between IDBC and SDBC.</p><p><strong>Results: </strong>Overall, the activity concentration obtained from the IDBC was lower than from the SDBC. When comparing IDBC with SDBC, variability was smallest for the ascending aorta (20.3% and 17.0% for <sup>89</sup>Zr-cetuximab and <sup>89</sup>Zr-durvalumab, respectively). Variability for the other regions ranged between 17.9 and 30.8%. Bias for the ascending aorta was - 10.9% and - 11.4% for <sup>89</sup>Zr-cetuximab and <sup>89</sup>Zr-durvalumab, respectively.</p><p><strong>Conclusions: </strong>Image-derived blood concentrations should be obtained from delineating the ascending aorta in <sup>89</sup>Zr-immuno-PET scans, as this results in the lowest variability with respect to sample-derived blood concentrations.</p>","PeriodicalId":11559,"journal":{"name":"EJNMMI Physics","volume":"11 1","pages":"16"},"PeriodicalIF":3.0000,"publicationDate":"2024-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10847076/pdf/","citationCount":"0","resultStr":"{\"title\":\"How to obtain the image-derived blood concentration from <sup>89</sup>Zr-immuno-PET scans.\",\"authors\":\"Jessica E Wijngaarden, Amina Ahbari, Johanna E E Pouw, Henri N J M Greuter, Idris Bahce, Gerben J C Zwezerijnen, Daniëlle J Vugts, Guus A M S van Dongen, Ronald Boellaard, C Willemien Menke-van der Houven van Oordt, Marc C Huisman\",\"doi\":\"10.1186/s40658-024-00621-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>PET scans using zirconium-89 labelled monoclonal antibodies (<sup>89</sup>Zr-mAbs), known as <sup>89</sup>Zr-immuno-PET, are made to measure uptake in tumour and organ tissue. Uptake is related to the supply of <sup>89</sup>Zr-mAbs in the blood. Measuring activity concentrations in blood, however, requires invasive blood sampling. This study aims to identify the best delineation strategy to obtain the image-derived blood concentration (IDBC) from <sup>89</sup>Zr-immuno-PET scans.</p><p><strong>Methods: </strong>PET imaging and blood sampling of two <sup>89</sup>Zr-mAbs were included, <sup>89</sup>Zr-cetuximab and <sup>89</sup>Zr-durvalumab. For seven patients receiving <sup>89</sup>Zr-cetuximab, PET scans on 1-2 h, 2 and 6 days post-injection (p.i.) were analysed. Five patients received three injections of <sup>89</sup>Zr-durvalumab. The scanning protocol for the first two injections consisted of PET scanning on 2, 5 and 7 days p.i. and for the third injection only on 7 days p.i. Blood samples were drawn with every PET scan and the sample-derived blood concentration (SDBC) was used as gold standard for the IDBC. According to an in-house developed standard operating procedure, the aortic arch, ascending aorta, descending aorta and left ventricle were delineated. Bland-Altman analyses were performed to assess the bias (mean difference) and variability (1.96 times the standard deviation of the differences) between IDBC and SDBC.</p><p><strong>Results: </strong>Overall, the activity concentration obtained from the IDBC was lower than from the SDBC. When comparing IDBC with SDBC, variability was smallest for the ascending aorta (20.3% and 17.0% for <sup>89</sup>Zr-cetuximab and <sup>89</sup>Zr-durvalumab, respectively). Variability for the other regions ranged between 17.9 and 30.8%. Bias for the ascending aorta was - 10.9% and - 11.4% for <sup>89</sup>Zr-cetuximab and <sup>89</sup>Zr-durvalumab, respectively.</p><p><strong>Conclusions: </strong>Image-derived blood concentrations should be obtained from delineating the ascending aorta in <sup>89</sup>Zr-immuno-PET scans, as this results in the lowest variability with respect to sample-derived blood concentrations.</p>\",\"PeriodicalId\":11559,\"journal\":{\"name\":\"EJNMMI Physics\",\"volume\":\"11 1\",\"pages\":\"16\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-02-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10847076/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"EJNMMI Physics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1186/s40658-024-00621-7\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"EJNMMI Physics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s40658-024-00621-7","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
引用次数: 0

摘要

背景:使用锆-89 标记的单克隆抗体(89Zr-mAbs)进行 PET 扫描,即 89Zr-immuno-PET 扫描,是为了测量肿瘤和器官组织的摄取量。摄取量与血液中 89Zr-mAbs 的供应量有关。然而,测量血液中的活性浓度需要进行侵入性血液采样。本研究旨在确定从 89Zr-immuno-PET 扫描中获取图像衍生血液浓度(IDBC)的最佳划分策略:研究纳入了两种 89Zr-mAbs (89Zr-西妥昔单抗和 89Zr-durvalumab)的 PET 成像和血液采样。对接受 89Zr-cetuximab 治疗的七名患者注射后 1-2 h、2 天和 6 天的 PET 扫描结果进行了分析。五名患者接受了三次 89Zr-durvalumab 注射。前两次注射的扫描方案包括注射后 2 天、5 天和 7 天的 PET 扫描,第三次注射只在注射后 7 天进行。每次 PET 扫描都会抽取血液样本,样本衍生血液浓度(SDBC)被用作 IDBC 的金标准。根据内部制定的标准操作程序,对主动脉弓、升主动脉、降主动脉和左心室进行了划定。对 IDBC 和 SDBC 的偏差(平均差)和变异性(差值标准差的 1.96 倍)进行了 Bland-Altman 分析:总体而言,IDBC 的活性浓度低于 SDBC。比较 IDBC 和 SDBC,升主动脉的变异性最小(89Zr-西妥昔单抗和 89Zr-durvalumab 分别为 20.3% 和 17.0%)。其他区域的变异性介于 17.9% 和 30.8% 之间。89Zr-西妥昔单抗和89Zr-durvalumab的升主动脉偏差分别为-10.9%和-11.4%:结论:在89Zr-免疫PET扫描中,应通过划定升主动脉来获得图像衍生血液浓度,因为这与样本衍生血液浓度相比变异性最小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
How to obtain the image-derived blood concentration from 89Zr-immuno-PET scans.

Background: PET scans using zirconium-89 labelled monoclonal antibodies (89Zr-mAbs), known as 89Zr-immuno-PET, are made to measure uptake in tumour and organ tissue. Uptake is related to the supply of 89Zr-mAbs in the blood. Measuring activity concentrations in blood, however, requires invasive blood sampling. This study aims to identify the best delineation strategy to obtain the image-derived blood concentration (IDBC) from 89Zr-immuno-PET scans.

Methods: PET imaging and blood sampling of two 89Zr-mAbs were included, 89Zr-cetuximab and 89Zr-durvalumab. For seven patients receiving 89Zr-cetuximab, PET scans on 1-2 h, 2 and 6 days post-injection (p.i.) were analysed. Five patients received three injections of 89Zr-durvalumab. The scanning protocol for the first two injections consisted of PET scanning on 2, 5 and 7 days p.i. and for the third injection only on 7 days p.i. Blood samples were drawn with every PET scan and the sample-derived blood concentration (SDBC) was used as gold standard for the IDBC. According to an in-house developed standard operating procedure, the aortic arch, ascending aorta, descending aorta and left ventricle were delineated. Bland-Altman analyses were performed to assess the bias (mean difference) and variability (1.96 times the standard deviation of the differences) between IDBC and SDBC.

Results: Overall, the activity concentration obtained from the IDBC was lower than from the SDBC. When comparing IDBC with SDBC, variability was smallest for the ascending aorta (20.3% and 17.0% for 89Zr-cetuximab and 89Zr-durvalumab, respectively). Variability for the other regions ranged between 17.9 and 30.8%. Bias for the ascending aorta was - 10.9% and - 11.4% for 89Zr-cetuximab and 89Zr-durvalumab, respectively.

Conclusions: Image-derived blood concentrations should be obtained from delineating the ascending aorta in 89Zr-immuno-PET scans, as this results in the lowest variability with respect to sample-derived blood concentrations.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
EJNMMI Physics
EJNMMI Physics Physics and Astronomy-Radiation
CiteScore
6.70
自引率
10.00%
发文量
78
审稿时长
13 weeks
期刊介绍: EJNMMI Physics is an international platform for scientists, users and adopters of nuclear medicine with a particular interest in physics matters. As a companion journal to the European Journal of Nuclear Medicine and Molecular Imaging, this journal has a multi-disciplinary approach and welcomes original materials and studies with a focus on applied physics and mathematics as well as imaging systems engineering and prototyping in nuclear medicine. This includes physics-driven approaches or algorithms supported by physics that foster early clinical adoption of nuclear medicine imaging and therapy.
期刊最新文献
Comparative analysis of positron emitters for theranostic applications based on small bioconjugates highlighting 43Sc, 61Cu and 45Ti. Impact of cell geometry, cellular uptake region, and tumour morphology on 225Ac and 177Lu dose distributions in prostate cancer. Optimization and application of renal depth measurement method in the cadmium-zinc-telluride‑based SPECT/CT renal dynamic imaging. How much do 68Ga-, 177Lu- and 131I-based radiopharmaceuticals contribute to the global radiation exposure of nuclear medicine staff? Comparison of the dosimetry and cell survival effect of 177Lu and 161Tb somatostatin analog radiopharmaceuticals in cancer cell clusters and micrometastases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1