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恶性淋巴瘤的铟-111 五肽胃泌素闪烁扫描术

Indium-111 pentetreotide scintigraphy in malignant lymphomas.

作者信息

Sarda L, Duet M, Zini J M, Berolatti B, Benelhadj S, Tobelem G, Mundler O

机构信息

Department of Nuclear Medicine, Lariboisière Hospital, Paris, France.

出版信息

Eur J Nucl Med. 1995 Oct;22(10):1105-9. doi: 10.1007/BF00800590.

Abstract

Somatostatin receptor imaging (SRI) was carried out as part of the initial staging of 26 patients with histologically proven Hodgkin's (3) and non-Hodgkin's (23) lymphoma, and in the assessment of the first treatment's efficacy in seven of these patients. Static acquisitions over the whole body were performed 4 and 24 h after intravenous administration of 150 MBq of indium-111 pentetreotide. SRI data were compared with the results of conventional methods (clinical data, abdominal and thoracic computed tomography, bone marrow biopsy). Only 50 of the 86 (58%) confirmed extra-medullary tumour sites were detected by SRI. Twelve previously unknown localizations were visualized in seven patients. The Ann Arbor clinical stage was modified in only one of them. When tumoral tracer uptake was present, a tumour uptake index (TUI) was calculated using two regions of interest (one over the tumoral hot spot and one over the shoulder) on 24-h planar images. The patients were classified into three groups: high tumour uptake (TUI > 2.5 in all tumour sites, group A, six patients), low tumour uptake (1.5 < TUI < 2.5 in all tumour sites, group B, 18 patients), and no tumour uptake (group C, two patients). The sensitivity of SRI detection was higher in group A (90%) than in group B (52%) (P < 0.001). Six weeks after the fourth chemotherapy cycle, conventional methods and SRI were concordant in five of seven investigated cases (four complete remissions and one residual active thoracic mass showing tracer uptake), and discordant in two. SRI demonstrated residual tumoral tracer uptake in these two patients, who had previously been considered to be in complete remission. In conclusion, SRI does not seem to be reliable for the initial staging of lymphomas because of the highly variable and usually low tumoral tracer uptake. It may be more useful in the diagnosis of residual masses after treatment. However, further studies are needed to assess its specificity.

摘要

生长抑素受体显像(SRI)作为26例经组织学证实的霍奇金淋巴瘤(3例)和非霍奇金淋巴瘤(23例)初始分期的一部分进行,并用于评估其中7例患者首次治疗的疗效。静脉注射150MBq铟-111喷替肽后4小时和24小时进行全身静态采集。将SRI数据与传统方法(临床数据、腹部和胸部计算机断层扫描、骨髓活检)的结果进行比较。SRI仅检测到86个(58%)已确认的髓外肿瘤部位中的50个。7例患者中发现了12个先前未知的肿瘤定位。其中只有1例患者的Ann Arbor临床分期发生了改变。当存在肿瘤示踪剂摄取时,在24小时平面图像上使用两个感兴趣区域(一个位于肿瘤热点上方,一个位于肩部上方)计算肿瘤摄取指数(TUI)。患者分为三组:高肿瘤摄取组(所有肿瘤部位TUI>2.5,A组,6例患者)、低肿瘤摄取组(所有肿瘤部位1.5<TUI<2.5,B组,18例患者)和无肿瘤摄取组(C组,2例患者)。A组SRI检测的敏感性(90%)高于B组(52%)(P<0.001)。在第四个化疗周期后6周,7例受调查病例中有5例传统方法和SRI结果一致(4例完全缓解,1例残留活动性胸部肿块显示有示踪剂摄取),2例不一致。SRI显示这2例患者有残留肿瘤示踪剂摄取,他们之前被认为已完全缓解。总之,由于肿瘤示踪剂摄取高度可变且通常较低,SRI对于淋巴瘤的初始分期似乎不可靠。它在治疗后残留肿块的诊断中可能更有用。然而,需要进一步研究来评估其特异性。

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