Cavalla P, Schiffer D
Department of Neuroscience, University of Turin, Italy.
Ann Oncol. 2001;12 Suppl 2:S131-4. doi: 10.1093/annonc/12.suppl_2.s131.
Somatostatin and other neuropeptides are expressed in tumors originating from neuronal precursors and paraganglia, namely medulloblastoma, central Primitive Neuro-Ectodermal Tumors (cPNETs), neurocytoma, gangliocytoma. olfactory neuroblastoma, paraganglioma. In medulloblastoma, the most common malignant tumor in childhood, there is an extensive expression of somatostatin in addition to somatostatin receptors (SSTR) type 2. Although density of SSTR-2 and intensity of expression of somatostatin genes have no prognostic significance in medulloblastoma. their presence may bring along important information on oncogenesis and relate medulloblastoma to cPNETs. Radio-labeled octreotide scintigraphy may be useful in the follow-up of these patients. allowing differentiation between scar and tumoral tissue. Moreover, on the basis of octreotide-induced inhibition of cell proliferation in medulloblastoma, a trial with octreotide in patients with recurrent or high-risk tumor is warranted. Meningiomas and low-grade astrocytic gliomas, even if not displaying a clear neuroendocrine phenotype, have high levels of SSTR-2. In meningiomas, SSTRs-scintigraphy is not part of the routine pre-operative assessment; moreover, a therapeutic trial with somatostatin-analogues in patients with recurrent or inoperable meningiomas should be carried-out with great caution, because somatostatin and octreotide slightly increase cell proliferation in cultured meningiomatous cells. Low-grade gliomas (WHO grade 2), and a smaller fraction of anaplastic astrocytomas, express SSTR-2, while glioblastomas usually do not. Unfortunately, radiolabeled-octreotide scintigraphy is not useful in the differential diagnosis of gliomas, because the results are altered by the disruption of the blood brain barrier (BBB); in addition, radionuclide-labeled somatostatin analogues are not useful in the therapy of low-grade gliomas, because the intact BBB prevents them from reaching the target SSTR-2. Recently, a pilot study in gliomas, has proposed the use of a radio-labeled somatostostatin analogue with a loco-regional approach in order to overcome the intact BBB.
生长抑素和其他神经肽在起源于神经前体和副神经节的肿瘤中表达,即髓母细胞瘤、中枢原始神经外胚层肿瘤(cPNETs)、神经细胞瘤、神经节细胞瘤、嗅神经母细胞瘤、副神经节瘤。在儿童最常见的恶性肿瘤髓母细胞瘤中,除了2型生长抑素受体(SSTR)外,生长抑素也有广泛表达。虽然SSTR-2的密度和生长抑素基因的表达强度在髓母细胞瘤中没有预后意义,但它们的存在可能会带来有关肿瘤发生的重要信息,并将髓母细胞瘤与cPNETs联系起来。放射性标记的奥曲肽闪烁扫描在这些患者的随访中可能有用,有助于区分瘢痕组织和肿瘤组织。此外,基于奥曲肽对髓母细胞瘤细胞增殖的抑制作用,对复发或高危肿瘤患者进行奥曲肽试验是有必要的。脑膜瘤和低级别星形细胞瘤,即使没有显示出明确的神经内分泌表型,也有高水平的SSTR-2。在脑膜瘤中,SSTR闪烁扫描不是常规术前评估的一部分;此外,对复发或无法手术的脑膜瘤患者进行生长抑素类似物治疗试验时应非常谨慎,因为生长抑素和奥曲肽会轻微增加培养的脑膜瘤细胞的增殖。低级别胶质瘤(WHO 2级)以及一小部分间变性星形细胞瘤表达SSTR-2,而胶质母细胞瘤通常不表达。不幸的是,放射性标记的奥曲肽闪烁扫描在胶质瘤的鉴别诊断中没有用,因为血脑屏障(BBB)的破坏会改变结果;此外,放射性核素标记的生长抑素类似物在低级别胶质瘤的治疗中也没有用,因为完整的血脑屏障会阻止它们到达目标SSTR-2。最近,一项在胶质瘤中的初步研究提出使用放射性标记的生长抑素类似物并采用局部区域方法,以克服完整的血脑屏障。