Trine Husby, Knut Johannessen, Erik Magnus Berntsen, Håkon Johansen, Guro Fanneløb Giskeødegård, Anna Karlberg, Unn-Merete Fagerli, Live Eikenes
{"title":"18F-FACBC 和 18F-FDG PET/MRI 在评估 3 名原发性中枢神经系统淋巴瘤患者中的应用:一项试点研究","authors":"Trine Husby, Knut Johannessen, Erik Magnus Berntsen, Håkon Johansen, Guro Fanneløb Giskeødegård, Anna Karlberg, Unn-Merete Fagerli, Live Eikenes","doi":"10.1186/s41824-024-00189-6","DOIUrl":null,"url":null,"abstract":"This PET/MRI study compared contrast-enhanced MRI, 18F-FACBC-, and 18F-FDG-PET in the detection of primary central nervous system lymphomas (PCNSL) in patients before and after high-dose methotrexate chemotherapy. Three immunocompetent PCNSL patients with diffuse large B-cell lymphoma received dynamic 18F-FACBC- and 18F-FDG-PET/MRI at baseline and response assessment. Lesion detection was defined by clinical evaluation of contrast enhanced T1 MRI (ce-MRI) and visual PET tracer uptake. SUVs and tumor-to-background ratios (TBRs) (for 18F-FACBC and 18F-FDG) and time-activity curves (for 18F-FACBC) were assessed. At baseline, seven ce-MRI detected lesions were also detected with 18F-FACBC with high SUVs and TBRs (SUVmax:mean, 4.73, TBRmax: mean, 9.32, SUVpeak: mean, 3.21, TBRpeak:mean: 6.30). High TBR values of 18F-FACBC detected lesions were attributed to low SUVbackground. Baseline 18F-FDG detected six lesions with high SUVs (SUVmax: mean, 13.88). In response scans, two lesions were detected with ce-MRI, while only one was detected with 18F-FACBC. The lesion not detected with 18F-FACBC was a small atypical MRI detected lesion, which may indicate no residual disease, as this patient was still in complete remission 12 months after initial diagnosis. No lesions were detected with 18F-FDG in the response scans. 18F-FACBC provided high tumor contrast, outperforming 18F-FDG in lesion detection at both baseline and in response assessment. 18F-FACBC may be a useful supplement to ce-MRI in PCNSL detection and response assessment, but further studies are required to validate these findings. Trial registration ClinicalTrials.gov. Registered 15th of June 2017 (Identifier: NCT03188354, https://clinicaltrials.gov/study/NCT03188354 ).","PeriodicalId":36160,"journal":{"name":"European Journal of Hybrid Imaging","volume":"8 1","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2024-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"18F-FACBC and 18F-FDG PET/MRI in the evaluation of 3 patients with primary central nervous system lymphoma: a pilot study\",\"authors\":\"Trine Husby, Knut Johannessen, Erik Magnus Berntsen, Håkon Johansen, Guro Fanneløb Giskeødegård, Anna Karlberg, Unn-Merete Fagerli, Live Eikenes\",\"doi\":\"10.1186/s41824-024-00189-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This PET/MRI study compared contrast-enhanced MRI, 18F-FACBC-, and 18F-FDG-PET in the detection of primary central nervous system lymphomas (PCNSL) in patients before and after high-dose methotrexate chemotherapy. Three immunocompetent PCNSL patients with diffuse large B-cell lymphoma received dynamic 18F-FACBC- and 18F-FDG-PET/MRI at baseline and response assessment. Lesion detection was defined by clinical evaluation of contrast enhanced T1 MRI (ce-MRI) and visual PET tracer uptake. SUVs and tumor-to-background ratios (TBRs) (for 18F-FACBC and 18F-FDG) and time-activity curves (for 18F-FACBC) were assessed. At baseline, seven ce-MRI detected lesions were also detected with 18F-FACBC with high SUVs and TBRs (SUVmax:mean, 4.73, TBRmax: mean, 9.32, SUVpeak: mean, 3.21, TBRpeak:mean: 6.30). High TBR values of 18F-FACBC detected lesions were attributed to low SUVbackground. Baseline 18F-FDG detected six lesions with high SUVs (SUVmax: mean, 13.88). In response scans, two lesions were detected with ce-MRI, while only one was detected with 18F-FACBC. The lesion not detected with 18F-FACBC was a small atypical MRI detected lesion, which may indicate no residual disease, as this patient was still in complete remission 12 months after initial diagnosis. No lesions were detected with 18F-FDG in the response scans. 18F-FACBC provided high tumor contrast, outperforming 18F-FDG in lesion detection at both baseline and in response assessment. 18F-FACBC may be a useful supplement to ce-MRI in PCNSL detection and response assessment, but further studies are required to validate these findings. Trial registration ClinicalTrials.gov. 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引用次数: 0
摘要
这项 PET/MRI 研究比较了对比增强 MRI、18F-FACBC 和 18F-FDG-PET 在检测大剂量甲氨蝶呤化疗前后患者原发性中枢神经系统淋巴瘤(PCNSL)方面的作用。三名免疫功能正常的弥漫大B细胞淋巴瘤PCNSL患者在基线和反应评估时接受了动态18F-FACBC-和18F-FDG-PET/MRI检查。病灶检测是通过对比增强 T1 MRI(ce-MRI)的临床评估和可视 PET 示踪剂摄取来定义的。对 SUV 和肿瘤-背景比 (TBR) (18F-FACBC 和 18F-FDG)以及时间-活性曲线(18F-FACBC)进行了评估。基线时,7 个 ce-MRI 检测到的病灶也用 18F-FACBC 检测到了高 SUV 和高 TBR(SUVmax:平均值为 4.73,TBRmax:平均值为 9.32,SUVpeak:平均值为 3.21,TBRpeak:平均值为 6.30):6.30).18F-FACBC 检测到的病灶的 TBR 值高是因为 SUV 背景低。基线 18F-FDG 检测到六个病灶的 SUV 值较高(SUVmax:平均值为 13.88)。在响应扫描中,ce-MRI 检测到两个病灶,而 18F-FACBC 仅检测到一个病灶。18F-FACBC未检测到的病灶是MRI检测到的一个小的非典型病灶,这可能表明没有残留疾病,因为该患者在初次诊断12个月后仍处于完全缓解状态。在反应扫描中,18F-FDG 没有检测到病灶。18F-FACBC 的肿瘤对比度高,在基线和反应评估的病灶检测中均优于 18F-FDG。在PCNSL检测和反应评估中,18F-FACBC可能是ce-MRI的有益补充,但还需要进一步的研究来验证这些发现。试验注册 ClinicalTrials.gov.2017年6月15日注册(标识符:NCT03188354,https://clinicaltrials.gov/study/NCT03188354 )。
18F-FACBC and 18F-FDG PET/MRI in the evaluation of 3 patients with primary central nervous system lymphoma: a pilot study
This PET/MRI study compared contrast-enhanced MRI, 18F-FACBC-, and 18F-FDG-PET in the detection of primary central nervous system lymphomas (PCNSL) in patients before and after high-dose methotrexate chemotherapy. Three immunocompetent PCNSL patients with diffuse large B-cell lymphoma received dynamic 18F-FACBC- and 18F-FDG-PET/MRI at baseline and response assessment. Lesion detection was defined by clinical evaluation of contrast enhanced T1 MRI (ce-MRI) and visual PET tracer uptake. SUVs and tumor-to-background ratios (TBRs) (for 18F-FACBC and 18F-FDG) and time-activity curves (for 18F-FACBC) were assessed. At baseline, seven ce-MRI detected lesions were also detected with 18F-FACBC with high SUVs and TBRs (SUVmax:mean, 4.73, TBRmax: mean, 9.32, SUVpeak: mean, 3.21, TBRpeak:mean: 6.30). High TBR values of 18F-FACBC detected lesions were attributed to low SUVbackground. Baseline 18F-FDG detected six lesions with high SUVs (SUVmax: mean, 13.88). In response scans, two lesions were detected with ce-MRI, while only one was detected with 18F-FACBC. The lesion not detected with 18F-FACBC was a small atypical MRI detected lesion, which may indicate no residual disease, as this patient was still in complete remission 12 months after initial diagnosis. No lesions were detected with 18F-FDG in the response scans. 18F-FACBC provided high tumor contrast, outperforming 18F-FDG in lesion detection at both baseline and in response assessment. 18F-FACBC may be a useful supplement to ce-MRI in PCNSL detection and response assessment, but further studies are required to validate these findings. Trial registration ClinicalTrials.gov. Registered 15th of June 2017 (Identifier: NCT03188354, https://clinicaltrials.gov/study/NCT03188354 ).