Somatostatin receptor scintigraphy in brain tumors and pituitary tumors: first experiences.

K Scheidhauer, G Hildebrandt, C Luyken, K Schomäcker, N Klug, H Schicha
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Abstract

Somatostatin receptors have been demonstrated on various tumors of neuroendocrine and other origin. They have been detected in vitro by biochemical techniques as well as by autoradiography. The development of long-acting somatostatin analogs and the recent availability of radiolabeled octreotide have made the in vivo detection of somatostatin receptors possible. This preliminary study embraced 45 patients with meningiomas, brain tumors or pituitary tumors, which were imaged by planar and tomographic scintigraphy after intravenous injection of 111Indium-labeled octreotide. In all of the meningiomas studied (unifocal and multifocal tumors in various locations), a high density of somatostatin receptors was detected by scintigraphy. Pituitary tumors were slightly positive in 50% of cases only, independent of the endocrine activity. Gliomas with an intact blood-brain barrier showed no enhanced tracer uptake in vivo, while gliomas with disturbed blood-brain barrier had a high activity uptake. We conclude that in vivo somatostatin receptor scintigraphy, although not tumor-specific, may aid in the preoperative diagnosis and staging of intracranial tumors, especially skull base tumors.

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脑肿瘤和垂体肿瘤的生长抑素受体闪烁成像:初步经验。
生长抑素受体已在各种神经内分泌和其他来源的肿瘤中得到证实。它们已被体外生化技术和放射自显影技术检测到。长效生长抑素类似物的发展和最近放射性标记奥曲肽的可用性使得体内检测生长抑素受体成为可能。本初步研究纳入45例脑膜瘤、脑肿瘤或垂体肿瘤患者,静脉注射111铟标记奥曲肽后行平面显像和断层显像。在所有研究的脑膜瘤(不同部位的单灶性和多灶性肿瘤)中,通过闪烁成像检测到高密度的生长抑素受体。垂体瘤仅在50%的病例中呈轻微阳性,与内分泌活动无关。具有完整血脑屏障的胶质瘤在体内未显示出增强的示踪剂摄取,而具有紊乱血脑屏障的胶质瘤具有高活性摄取。我们的结论是,体内生长抑素受体显像虽然不是肿瘤特异性的,但可能有助于颅内肿瘤,特别是颅底肿瘤的术前诊断和分期。
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Diabetes Care and Research in Europe. 3rd European meeting for the Implementation of the St. Vincent Declaration. Athens, Greece, March 29-April 1, 1995. Abstracts. Molecular mechanisms of somatostatin's inhibition of hormone release: participation of voltage-gated calcium channels and G-proteins. Somatostatin Receptor Imaging. 1st German meeting. Stuttgart, September 1992. Biodistribution of 111In-pentetreotide and dosimetric considerations with respect to somatostatin receptor expressing tumor burden. Receptor scintigraphy with 111In-pentetreotide for endocrine gastroenteropancreatic tumors.
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