The value of radiolabelled MIBG and octreotide in the diagnosis and management of neuroendocrine tumours.
Neuroendocrine tumours have a particular tendency to express functional receptors and/or uptake mechanisms. Radionuclides, such as 123I-MIBG, which is taken up by a specific uptake mechanism, and 111In-pentetreotide, which binds to somatostatin receptors, present an imaging modality based on these p...
| Main Authors: | , , |
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| Format: | Journal article |
| Language: | English |
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2001
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| _version_ | 1797065894050922496 |
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| author | Kaltsas, G Mukherjee, J Grossman, AB |
| author_facet | Kaltsas, G Mukherjee, J Grossman, AB |
| author_sort | Kaltsas, G |
| collection | OXFORD |
| description | Neuroendocrine tumours have a particular tendency to express functional receptors and/or uptake mechanisms. Radionuclides, such as 123I-MIBG, which is taken up by a specific uptake mechanism, and 111In-pentetreotide, which binds to somatostatin receptors, present an imaging modality based on these physiological characteristics rather on purely anatomical alterations. They have been successfully utilised for both the diagnosis and staging of neuroendocrine tumours, as they can identify lesions beyond the diagnostic sensitivity of conventional imaging modalities. Scintigraphy with 111In-pentetreotide is in general more sensitive but scintigraphy with 123I-MIBG may occasionally demonstrate lesions not evident with 111In-pentetreotide. Although both are effective in identifying hepatic metastases there may be quantitative and qualitative differences in the pattern of uptake. 131I-MIBG therapy, based on a positive 123I-MIBG scan, produces symptomatic and hormonal improvement and moderate tumour regression/stabilisation in many patients with metastatic neuroendocrine tumours with minimal adverse effects. It may be a valuable alternative or additional therapeutic option to the currently available conventional treatment modalities. Although experience with 90Y-DOTA-D-Phe1-Tyr3-octreotide therapy is still limited, preliminary studies have demonstrated useful activity in tumours with positive 111In-pentetreotide scans, and yet other radionuclide analogues may become available. However, treatment with the combination of both radionuclides is another therapeutic possibility. |
| first_indexed | 2024-03-06T21:34:51Z |
| format | Journal article |
| id | oxford-uuid:45e0907b-f4e3-4037-b385-6ed93b06a456 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-06T21:34:51Z |
| publishDate | 2001 |
| record_format | dspace |
| spelling | oxford-uuid:45e0907b-f4e3-4037-b385-6ed93b06a4562022-03-26T15:10:30ZThe value of radiolabelled MIBG and octreotide in the diagnosis and management of neuroendocrine tumours.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:45e0907b-f4e3-4037-b385-6ed93b06a456EnglishSymplectic Elements at Oxford2001Kaltsas, GMukherjee, JGrossman, ABNeuroendocrine tumours have a particular tendency to express functional receptors and/or uptake mechanisms. Radionuclides, such as 123I-MIBG, which is taken up by a specific uptake mechanism, and 111In-pentetreotide, which binds to somatostatin receptors, present an imaging modality based on these physiological characteristics rather on purely anatomical alterations. They have been successfully utilised for both the diagnosis and staging of neuroendocrine tumours, as they can identify lesions beyond the diagnostic sensitivity of conventional imaging modalities. Scintigraphy with 111In-pentetreotide is in general more sensitive but scintigraphy with 123I-MIBG may occasionally demonstrate lesions not evident with 111In-pentetreotide. Although both are effective in identifying hepatic metastases there may be quantitative and qualitative differences in the pattern of uptake. 131I-MIBG therapy, based on a positive 123I-MIBG scan, produces symptomatic and hormonal improvement and moderate tumour regression/stabilisation in many patients with metastatic neuroendocrine tumours with minimal adverse effects. It may be a valuable alternative or additional therapeutic option to the currently available conventional treatment modalities. Although experience with 90Y-DOTA-D-Phe1-Tyr3-octreotide therapy is still limited, preliminary studies have demonstrated useful activity in tumours with positive 111In-pentetreotide scans, and yet other radionuclide analogues may become available. However, treatment with the combination of both radionuclides is another therapeutic possibility. |
| spellingShingle | Kaltsas, G Mukherjee, J Grossman, AB The value of radiolabelled MIBG and octreotide in the diagnosis and management of neuroendocrine tumours. |
| title | The value of radiolabelled MIBG and octreotide in the diagnosis and management of neuroendocrine tumours. |
| title_full | The value of radiolabelled MIBG and octreotide in the diagnosis and management of neuroendocrine tumours. |
| title_fullStr | The value of radiolabelled MIBG and octreotide in the diagnosis and management of neuroendocrine tumours. |
| title_full_unstemmed | The value of radiolabelled MIBG and octreotide in the diagnosis and management of neuroendocrine tumours. |
| title_short | The value of radiolabelled MIBG and octreotide in the diagnosis and management of neuroendocrine tumours. |
| title_sort | value of radiolabelled mibg and octreotide in the diagnosis and management of neuroendocrine tumours |
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