99mTc-HYNIC octreotide in neuroblastoma.

Ann Nucl Med

Nuclear Medicine Center, Clinical Hospital, University of Uruguay, Av. Italia s/n, C.P. 11600, Montevideo, Uruguay.

Published: November 2008

AI Article Synopsis

  • Neuroblastoma disease assessment typically involves CT, MRI, bone scans, MIBG scans, bone marrow tests, and urine catecholamine measurements.
  • A case study of an 8-year-old boy with stage-IV neuroblastoma showed that scans using technetium-99m-HYNIC-octreotide detected more tumor spread compared to the standard iodin-131-MIBG scan.
  • The findings suggest that 99mTc-HYNIC-octreotide could be a valuable imaging agent for neuroblastoma and warrant further clinical trials.

Article Abstract

Disease status assessment of neuroblastoma patients requires computed tomography (or magnetic resonance imaging), bone scan, metaiodobenzylguanidine (MIBG) scan, bone marrow tests, and urine catecholamine measurements. There is no clinical experience concerning the evaluation of these patients by means of technetium-99m (99mTc)-somatostatin analog scintigraphy. Furthermore, these radiopharmaceuticals are promising imaging agents owing to their lower cost, availability, dosimetry, and ease of preparation. An 8-year-old boy already diagnosed with stage-IV neuroblastoma received chemotherapy. In the follow-up, after obtaining the parents' informed consent, iodin 131 (131I)-MIBG and 99mTc-6-hydrazinopyridine-3-carboxylic acid (HYNIC)-octreotide scans were done on separate days to evaluate tumor extension. Even as the 131I-IBG scan showed mild diffuse uptake in the projection of both lung hili, the 99mTc-HYNIC-octreotide scan showed multiple axial and appendicular bone uptakes and paravertebral, abdominal, mediastinal, and supraclavicular ganglionar uptakes. The 99mTc-HYNIC-octreotide showed much more lesion extension than the 131I-MIBG. Therefore, 99mTc-HYNIC-octreotide may be a promising radiopharmaceutical for the evaluation of neuroblastoma patients. This finding justifies the preliminary evaluation of this tracer in the context of a clinical trial.

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Source
http://dx.doi.org/10.1007/s12149-008-0201-9DOI Listing

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