Radionuclide Imaging of Apoptosis in Malignancies: Promise and Pitfalls of Tc-Hynic-rh-Annexin V Imaging.

Clinical medicine. Oncology Pub Date : 2008-01-01 Epub Date: 2008-03-25 DOI:10.4137/cmo.s349
M S Kartachova, M Verheij, B L van Eck, C A Hoefnagel, R A Valdes Olmos
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引用次数: 8

Abstract

Radionuclide detection of apoptosis with of (99m)Tc-Hynic-rh-Annexin V scintigraphy is an effective tool for in vivo visualisation and monitoring of apoptosis in various malignant tumour. Early therapy-induced increase of the tumour tracer uptake correlates with favourable outcome, whereas stable or decreased uptake correlates with stable disease or tumour progression. Therefore sequential (99m)Tc-Hynic-rh-Annexin V scintigraphy could be used to predict therapy outcome on a patient-to-patient basis within 48 hours after the start of treatment. However, moderate tumour-to-background ratio and therapy-induced changes in normal tissues could confound image analysis. To assure accurate interpretation of Annexin V scans, the awareness of the biophysiological and biochemical properties contributing to the tracer distribution is essential. In with manuscript we discuss the patterns of Annexin V tumour uptake and illustrate the most frequent pitfalls associated with Annexin V imaging in correlation with CT and MRI imaging.

Abstract Image

Abstract Image

Abstract Image

恶性肿瘤细胞凋亡的放射性核素成像:Tc-Hynic-rh-Annexin V成像的希望与缺陷。
放射性核素检测凋亡的(99m) tc - hyic -rh- annexin V显像是在体内观察和监测各种恶性肿瘤细胞凋亡的有效工具。早期治疗诱导的肿瘤示踪剂摄取增加与有利的结果相关,而稳定或减少摄取与稳定的疾病或肿瘤进展相关。因此,序贯(99m) tc - hyic -rh- annexin V显像可用于预测治疗开始后48小时内患者间的治疗结果。然而,正常组织中适度的肿瘤与背景比和治疗引起的变化可能会混淆图像分析。为了确保膜联蛋白V扫描的准确解释,对示踪剂分布的生物生理和生化特性的认识是必不可少的。在我们的手稿中,我们讨论了膜联蛋白V肿瘤摄取的模式,并说明了与CT和MRI成像相关的膜联蛋白V成像最常见的陷阱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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