Carrasquillo Jorge A, Pandit-Taskar Neeta, Chen Clara C
Molecular Imaging and Therapy Service, Department of Radiology, Memorial Sloan Kettering, New York, NY; Department of Radiology, Weill Cornell Medical Center, New York, NY.
Molecular Imaging and Therapy Service, Department of Radiology, Memorial Sloan Kettering, New York, NY; Department of Radiology, Weill Cornell Medical Center, New York, NY.
Semin Nucl Med. 2016 May;46(3):203-14. doi: 10.1053/j.semnuclmed.2016.01.011.
Pheochromocytomas and paragangliomas are rare tumors arising from chromaffin cells. Available therapeutic modalities consist of chemotherapy, tyrosine kinase inhibitors, and I-131 metaiodobenzylguanidine (MIBG). I-131 MIBG is taken up via specific receptors and localizes into many but not all pheochromocytomas and paragangliomas. Because these tumors are rare, most therapy studies are retrospective presentations of clinical experience. Numerous retrospective studies and a few prospective studies have shown favorable responses in this disease, including symptomatic, biochemical, and objective responses. In this report, we review the experience of using I-131 MIBG therapy for targeting pheochromocytoma and paragangliomas.
嗜铬细胞瘤和副神经节瘤是起源于嗜铬细胞的罕见肿瘤。现有的治疗方式包括化疗、酪氨酸激酶抑制剂和碘-131间碘苄胍(MIBG)。碘-131 MIBG通过特定受体摄取,并定位于许多但并非所有的嗜铬细胞瘤和副神经节瘤中。由于这些肿瘤较为罕见,大多数治疗研究都是临床经验的回顾性报告。众多回顾性研究和少数前瞻性研究均显示该疾病对此有良好反应,包括症状性、生化指标及客观反应。在本报告中,我们回顾了使用碘-131 MIBG治疗嗜铬细胞瘤和副神经节瘤的经验。