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A Call for Common Sense in the Use of Molecular Imaging. 呼吁在分子成像应用中建立常识。
IF 9.1 Pub Date : 2025-09-02 DOI: 10.2967/jnumed.125.270550
Ida Skarping, Thuy Tran, Rimma Axelsson, Renske Altena
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引用次数: 0
Differential Association of PET-Derived Rest and Stress Myocardial Blood Flow with Cardiovascular Outcomes. pet衍生的休息和应激心肌血流量与心血管结局的差异关联。
IF 9.1 Pub Date : 2025-09-02 DOI: 10.2967/jnumed.125.269457
Ahmed Sayed, Mahmoud Al Rifai, Mouaz Al-Mallah

Although there is strong evidence for the prognostic value of myocardial flow reserve (MFR), there are fewer data on the prognostic implications of its constituents: myocardial blood flow at rest (MBFrest) and stress (MBFstress). Methods: Consecutive patients undergoing 82Rb PET imaging with regadenoson stress testing at a tertiary care center between August 2019 and August 2024 were included in this study. The 2 coprimary outcomes were a composite of death or heart failure (HF) hospitalization and a composite of myocardial infarction (MI) or late revascularization. Multivariable Andersen-Gill Cox models with robust variance estimators were used to incorporate recurrent events. Outcomes were modeled as a smooth function of MBFstress and MBFrest, with restricted cubic splines to allow nonlinearity. Results: The analysis included 8,131 consecutive patients (median age of 68 y; 46.1% were women; median follow-up of 520 d (interquartile range, 186-921 d), among whom 471 deaths, 828 HF hospitalizations, 164 MIs, and 429 late revascularizations occurred. After adjusting for the relevant covariates, an MFR of 2 achieved through a lower MBFrest was associated with a significantly lower incidence of death and HF hospitalization, whereas an MFR of 2 achieved through a greater MBFstress was associated with a significantly lower incidence of MI and late revascularization. Assessments of the partial χ2 statistic, which measures the importance of predictors, similarly confirmed that MBFrest was more important for predicting death or HF hospitalization whereas MBFstress was more important for predicting MI or late revascularization. Conclusion: Measurements of absolute myocardial blood flow offer complementary prognostic value to MFR. A diminished MBFstress may signal a greater risk of future ischemic outcomes, whereas an elevated MBFrest may signal a greater risk of future death or HF hospitalization.

虽然有强有力的证据表明心肌血流储备(MFR)的预后价值,但关于其成分:静息心肌血流(MBFrest)和应激心肌血流(MBFstress)的预后意义的数据较少。方法:本研究纳入2019年8月至2024年8月在某三级保健中心连续接受82Rb PET成像和regadenoson压力测试的患者。2个主要结局是死亡或心力衰竭住院的复合结局和心肌梗死(MI)或晚期血运重建术的复合结局。使用具有稳健方差估计的多变量Andersen-Gill Cox模型来合并复发事件。结果建模为mbf应力和mbf的光滑函数,并使用限制三次样条以允许非线性。结果:分析纳入了8131例连续患者(中位年龄68岁;女性占46.1%;中位随访时间为520天(四分位数范围为186-921天),其中471例死亡,828例心衰住院,164例心肌梗死,429例晚期血循环重建术。在对相关协变量进行调整后,通过较低的mbst达到2的MFR与较低的死亡发生率和HF住院率相关,而通过较高的mbst达到2的MFR与较低的心肌梗死发生率和较晚的血流量重建相关。对部分χ2统计量的评估(衡量预测因素的重要性)同样证实,MBFrest对于预测死亡或HF住院更重要,而MBFstress对于预测心肌梗死或晚期血运重建更重要。结论:心肌绝对血流量测量对MFR的预后有补充价值。mbf压力降低可能预示着未来缺血性结局的风险增加,而mbf压力升高可能预示着未来死亡或HF住院的风险增加。
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引用次数: 0
Precision Medicine Is Critical for the Future of Oncology: Johannes Czernin and Ken Herrmann Talk with Chris Behrenbruch on Theranostics, Imaging, and the Urgency to Innovate. 精准医学对肿瘤学的未来至关重要:Johannes Czernin和Ken Herrmann与Chris Behrenbruch讨论治疗学、成像和创新的紧迫性。
IF 9.1 Pub Date : 2025-09-02 DOI: 10.2967/jnumed.125.270966
Christian Behrenbruch, Ken Herrmann, Johannes Czernin
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引用次数: 0
Rapid Predictive Dosimetry Is Now Freely Available. 快速预测剂量法现在是免费的。
IF 9.1 Pub Date : 2025-09-02 DOI: 10.2967/jnumed.125.270536
Yung Hsiang Kao
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引用次数: 0
Distinct Prognostic Roles of 18F-FDG PET Metabolic Response Assessed After Induction Chemotherapy or Chemoradiotherapy in Localized Esophageal Squamous Cell Carcinoma. 18F-FDG - PET代谢反应在局部食管鳞状细胞癌诱导化疗或放化疗后的预后作用
IF 9.1 Pub Date : 2025-09-02 DOI: 10.2967/jnumed.125.269775
Yeong Hak Bang, Jong Hoon Kim, Yong-Hee Kim, Hyeong Ryul Kim, Jin-Sook Ryu, Yong-Il Kim, Joon Seon Song, Sung-Bae Kim, Sook Ryun Park

The prognostic significance of metabolic response by posttreatment 18F-FDG PET in esophageal squamous cell carcinoma (ESCC) treated with chemoradiotherapy remains unclear, particularly regarding metabolic response after induction chemotherapy versus after chemoradiotherapy. This study aimed to evaluate and compare their prognostic impact. Methods: This retrospective study analyzed 604 patients with localized ESCC who received induction chemotherapy followed by chemoradiotherapy, with or without surgery, at Asan Medical Center between 2006 and 2018. Metabolic responses after induction chemotherapy (before chemoradiotherapy) and after chemoradiotherapy were evaluated using European Organisation for Research and Treatment of Cancer-based criteria adapted for prognostic assessment. Results: In patients treated with definitive chemoradiotherapy (bimodality therapy), metabolic response after both induction chemotherapy and chemoradiotherapy was significantly associated with progression-free survival (PFS) and overall survival (OS). Complete metabolic response after induction chemotherapy correlated with the longest survival (PFS, 58.9 mo; OS, 90.8 mo), whereas progressive metabolic disease predicted poor prognosis (PFS, 3.7 mo; OS, 7.0 mo; P < 0.001). A similar pattern was observed for postchemoradiotherapy metabolic response. In patients who underwent surgery (trimodality therapy), metabolic response after induction chemotherapy did not significantly impact survival. However, in patients for whom surgery was initially planned, it remained prognostic, suggesting its prognostic relevance in the preoperative setting. Postchemoradiotherapy metabolic response was a strong independent prognostic factor in both bimodality therapy and trimodal therapy. Patients with diffuse esophagitis after chemoradiotherapy had intermediate survival outcomes, among complete metabolic response and partial metabolic response groups, indicating a distinct prognostic pattern. Conclusion: Postchemoradiotherapy metabolic response is a strong prognostic marker in localized ESCC, supporting its use for risk stratification. Early metabolic response after induction chemotherapy may also inform treatment decisions, particularly in surgery-intended patients.

食管鳞状细胞癌(ESCC)放化疗后18F-FDG PET代谢反应的预后意义尚不清楚,特别是诱导化疗后与放化疗后的代谢反应。本研究旨在评估和比较它们对预后的影响。方法:本回顾性研究分析了2006年至2018年峨山医疗中心604例局部ESCC患者,这些患者接受了诱导化疗和放化疗,伴或不伴手术。诱导化疗后(放化疗前)和放化疗后的代谢反应采用欧洲癌症研究和治疗组织的预后评估标准进行评估。结果:在接受终期放化疗(双峰治疗)的患者中,诱导化疗和放化疗后的代谢反应与无进展生存期(PFS)和总生存期(OS)显著相关。诱导化疗后完全代谢缓解与最长生存期(PFS, 58.9个月;OS, 90.8个月),而进行性代谢性疾病预测预后不良(PFS, 3.7个月;OS, 7.0 mo;P < 0.001)。在放化疗后的代谢反应中也观察到类似的模式。在接受手术(三段式治疗)的患者中,诱导化疗后的代谢反应对生存率没有显著影响。然而,在最初计划手术的患者中,它仍然是预后,表明其与术前设置的预后相关。放化疗后代谢反应在双峰治疗和三峰治疗中都是一个强大的独立预后因素。在完全代谢缓解组和部分代谢缓解组中,放化疗后弥漫性食管炎患者的生存结果中等,表明预后模式不同。结论:放化疗后代谢反应是局限性ESCC的一个强有力的预后指标,支持将其用于风险分层。诱导化疗后的早期代谢反应也可以为治疗决策提供信息,特别是在手术患者中。
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引用次数: 0
Foregoing Nonclinical Dosimetry Studies to Support First-in-Human Studies of Certain PET Radiopharmaceuticals. 上述非临床剂量学研究支持某些PET放射性药物的首次人体研究。
IF 9.1 Pub Date : 2025-09-02 DOI: 10.2967/jnumed.125.270320
Donika Plyku, Hayoung Koo, Luke Park, August Hofling, Libero Marzella
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引用次数: 0
Reply to "Foregoing Nonclinical Dosimetry Studies to Support First-in-Human Studies of Certain PET Radiopharmaceuticals". 回复“上述非临床剂量学研究以支持某些PET放射性药物的首次人体研究”。
IF 9.1 Pub Date : 2025-09-02 DOI: 10.2967/jnumed.125.270467
Marianna Dakanali, Steven S Zigler, Sally W Schwarz, Michael L Nickels, Reiko Oyama, Henry F VanBrocklin, Peter J H Scott
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引用次数: 0
Redefining Nuclear Medicine: "Biodistribution" Should Be the Core Concept. 重新定义核医学:“生物分布”应该是核心概念。
IF 9.1 Pub Date : 2025-09-02 DOI: 10.2967/jnumed.125.270245
Celso Dario Ramos
{"title":"Redefining Nuclear Medicine: \"Biodistribution\" Should Be the Core Concept.","authors":"Celso Dario Ramos","doi":"10.2967/jnumed.125.270245","DOIUrl":"10.2967/jnumed.125.270245","url":null,"abstract":"","PeriodicalId":94099,"journal":{"name":"Journal of nuclear medicine : official publication, Society of Nuclear Medicine","volume":" ","pages":"1498"},"PeriodicalIF":9.1,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144129727","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[68Ga]Ga-FAPI PET/CT Monitors Response to Receptor Activator of Nuclear Factor-κB Ligand Inhibitor in a Giant Cell Tumor of Bone: Correlation with Histopathology. [68Ga]Ga-FAPI PET/CT监测骨巨细胞瘤对核因子-κB配体抑制剂受体激活物的反应:与组织病理学的相关性。
IF 9.1 Pub Date : 2025-09-02 DOI: 10.2967/jnumed.124.269432
Wenjie Zhang, Wenqing Yao, Guohua Shen
{"title":"[<sup>68</sup>Ga]Ga-FAPI PET/CT Monitors Response to Receptor Activator of Nuclear Factor-κB Ligand Inhibitor in a Giant Cell Tumor of Bone: Correlation with Histopathology.","authors":"Wenjie Zhang, Wenqing Yao, Guohua Shen","doi":"10.2967/jnumed.124.269432","DOIUrl":"10.2967/jnumed.124.269432","url":null,"abstract":"","PeriodicalId":94099,"journal":{"name":"Journal of nuclear medicine : official publication, Society of Nuclear Medicine","volume":" ","pages":"1493"},"PeriodicalIF":9.1,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144083014","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Rare Influenza B Virus-Associated Cerebellitis Detected by 18F-FDG PET/CT Imaging. 18F-FDG PET/CT检测1例罕见乙型流感病毒相关小脑炎。
IF 9.1 Pub Date : 2025-09-02 DOI: 10.2967/jnumed.125.269548
Hukui Sun, Dayan Cheng, Xiangde Du, Chengwei Sun, Jiahui Zhang
{"title":"A Rare Influenza B Virus-Associated Cerebellitis Detected by <sup>18</sup>F-FDG PET/CT Imaging.","authors":"Hukui Sun, Dayan Cheng, Xiangde Du, Chengwei Sun, Jiahui Zhang","doi":"10.2967/jnumed.125.269548","DOIUrl":"10.2967/jnumed.125.269548","url":null,"abstract":"","PeriodicalId":94099,"journal":{"name":"Journal of nuclear medicine : official publication, Society of Nuclear Medicine","volume":" ","pages":"1494"},"PeriodicalIF":9.1,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143733824","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Journal of nuclear medicine : official publication, Society of Nuclear Medicine
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