肿瘤索马他汀 PET 检查心肌摄取的相关因素以及与急性心肌炎心肌摄取的区别

Thomas Larive, Caroline Boursier, Marine Claudin, Jeanne Varlot, Laura Filippetti, Olivier Huttin, Véronique Roch, Laetitia Imbert, Matthieu Doyen, Aurélien Lambert, Damien Mandry, Zohra Lamiral, Elodie Chevalier, Pierre-Yves Marie
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引用次数: 0

摘要

不仅在大多数急性心肌炎(AM)患者中,而且在一些转诊进行常规体生长抑素 PET 检查的肿瘤患者中,都能观察到心肌体生长抑素 PET 摄取。这引起了人们对体生长抑素 PET 检测心肌炎特异性的担忧。本研究旨在确定因肿瘤适应症而记录的体生长抑素 PET 扫描中发现心肌摄取的相关因素,以及鉴别 AM 患者心肌摄取特征的 PET 标准。方法:我们分析了在178名患者的508次[68Ga]Ga-DOTATOC PET扫描中发现心肌[68Ga]Ga-DOTATOC摄取的相关因素,这些扫描是为确诊或疑似肿瘤疾病(Onc-PET)而进行的,我们还分析了可将31名经MRI确诊的AM(AM-PET)患者的心肌[68Ga]Ga-DOTATOC摄取与Onc-PET组的心肌[68Ga]Ga-DOTATOC摄取区分开来的PET标准。结果:137例(26.9%)Onc-PET扫描中检测到明显的心肌摄取,且与体生长激素类似物治疗(exp(β),0.805;95% CI,0.728-0.890;P < 0.001)和年龄(exp(β),1.005;95% CI,1.001-1.009;P = 0.012)独立相关。使用体生长抑素类似物治疗(P < 0.001)和冠状动脉疾病史(P = 0.022)预测心肌-血液 SUVmax 比值的模型具有可比性。在接受过体生长激素类似物治疗的患者中,有12.9%(25/193)的Onc-PET扫描结果检测到心肌摄取,但在中位年龄为64岁的未接受过治疗的患者中,有43.4%(59/136)的扫描结果检测到心肌摄取。在所有 31 例 AM-PET 扫描中,心肌摄取都很明显,摄取量和摄取强度显著高于显示心肌摄取的 137 例 Onc-PET 扫描。心肌-血液 SUVmax 比值阈值为 2.20 时,区分 AM-PET 组和 Onc-PET 组心肌摄取的灵敏度为 87%(27/31),特异度为 88%(44/50),Onc-PET 组患者的临床特征与 AM-PET 组患者相似(年龄≤64 岁、无冠状动脉疾病史、无体生长抑素激动剂)。心肌摄取容积阈值为 18 cm3,诊断准确性相当(敏感性为 84% [26/31];特异性为 94% [47/50])。结论:在 26.9% 的肿瘤适应症体生长抑素 PET 扫描中检测到心肌摄取。体生长抑素类似物治疗会降低这一比例,而老年人的这一比例则会升高。不过,以摄取强度或体积为定量标准进行分析的体生长激素 PET 扫描能够识别 AM,并将其与其他原因引起的心肌摄取区分开来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors Associated with Myocardial Uptake on Oncologic Somatostatin PET Investigations and Differentiation from Myocardial Uptake of Acute Myocarditis.

Myocardial somatostatin PET uptake is observed not only in most patients with acute myocarditis (AM) but also in some oncology patients referred for routine somatostatin PET. This raises concerns about the specificity of somatostatin PET for detecting myocarditis. The current study aims to identify factors associated with the detection of myocardial uptake on somatostatin PET scans recorded for oncology indications and differential PET criteria that characterize myocardial uptake in AM patients. Methods: We analyzed factors associated with the detection of myocardial [68Ga]Ga-DOTATOC uptake in 508 [68Ga]Ga-DOTATOC PET scans from 178 patients, performed for confirmed or suspected oncologic disease (Onc-PET) and PET criteria that could differentiate myocardial [68Ga]Ga-DOTATOC uptake in 31 patients with MRI-ascertained AM (AM-PET) from that in the Onc-PET group. Results: Significant myocardial uptake was detected in 137 (26.9%) Onc-PET scans and was independently associated with somatostatin analog treatment (exp(β), 0.805; 95% CI, 0.728-0.890; P < 0.001) and age (exp(β), 1.005; 95% CI, 1.001-1.009; P = 0.012). A comparable model was selected for predicting the myocardial-to-blood SUVmax ratio using somatostatin analog treatment (P < 0.001) and history of coronary artery disease (P = 0.022). Myocardial uptake was detected in 12.9% (25/193) of Onc-PET scans from patients treated with somatostatin analogs but in 43.4% (59/136) of untreated patients over the median age of 64 y. Myocardial uptake was apparent in all 31 AM-PET scans, with volume and intensity of uptake dramatically higher than in the 137 Onc-PET scans showing myocardial uptake. A myocardial-to-blood SUVmax ratio threshold of 2.20 provided a sensitivity of 87% (27/31) and a specificity of 88% (44/50) for differentiating myocardial uptake between the AM-PET group and an Onc-PET group restricted to patients with clinical characteristics comparable to those of patients in the AM-PET group (≤64 y of age, no coronary artery disease history, and no somatostatin agonists). A myocardial uptake volume threshold of 18 cm3 provided comparable diagnostic accuracy (sensitivity, 84% [26/31]; specificity, 94% [47/50]). Conclusion: Myocardial uptake was detected in 26.9% of somatostatin PET scans recorded for oncology indications. This rate was decreased by somatostatin analog treatments and increased in older individuals. However, somatostatin PET scans, analyzed with the quantitative criterion of uptake intensity or volume, are able to identify AM and to differentiate it from myocardial uptake of other origins.

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