Sequelae and survivorship in patients treated with 131 I-MIBG therapy
Background: 131 I-meta-iodobenzylguanidine (131 I-MIBG) has been in therapeutic use since 1980s. Newer treatment modalities are emerging for neuroendocrine tumours (NETs) and chromaffin cell tumours (CCTs), but many of these do not yet have adequate long-term follow-up to determine their longer term...
| Main Authors: | , , , , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2013
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| _version_ | 1826288086720446464 |
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| author | Sze, W Grossman, AB Goddard, I Amendra, D Shieh, S Plowman, P Drake, WM Akker, SA Druce, MR |
| author_facet | Sze, W Grossman, AB Goddard, I Amendra, D Shieh, S Plowman, P Drake, WM Akker, SA Druce, MR |
| author_sort | Sze, W |
| collection | OXFORD |
| description | Background: 131 I-meta-iodobenzylguanidine (131 I-MIBG) has been in therapeutic use since 1980s. Newer treatment modalities are emerging for neuroendocrine tumours (NETs) and chromaffin cell tumours (CCTs), but many of these do not yet have adequate long-term follow-up to determine their longer term efficacy and sequelae. Methods: Fifty-eight patients with metastatic NETs and CCTs who had received 131 I-MIBG therapy between 2000 and 2011 were analysed. Survival and any long-term haematological or renal sequelae were investigated.Results:In the NET group, the overall median survival and median survival following the diagnosis of metastatic disease was 124 months. The median survival following the commencement of 131 I-MIBG was 66 months. For the CCT group, median survival had not been reached. The 5-year survival from diagnosis and following the diagnosis of metastatic disease was 67% and 67.5% for NETs and CCTs, respectively. The 5-year survival following the commencement of 131 I-MIBG therapy was 68%. Thirty-two patients had long-term haematological sequelae: 5 of these 32 patients developed haematological malignancies. Two patients developed a mild deterioration in renal function. Conclusion: Long follow up of 131 I-MIBG therapy reveals a noteable rate of bone marrow toxicities and malignancy and long term review of all patients receiving radionuclide therapies is recommended. © 2013 Cancer Research UK. All rights reserved. |
| first_indexed | 2024-03-07T02:08:26Z |
| format | Journal article |
| id | oxford-uuid:9fc96bdc-9b73-4e80-9a46-575927da435e |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T02:08:26Z |
| publishDate | 2013 |
| record_format | dspace |
| spelling | oxford-uuid:9fc96bdc-9b73-4e80-9a46-575927da435e2022-03-27T02:00:26ZSequelae and survivorship in patients treated with 131 I-MIBG therapyJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:9fc96bdc-9b73-4e80-9a46-575927da435eEnglishSymplectic Elements at Oxford2013Sze, WGrossman, ABGoddard, IAmendra, DShieh, SPlowman, PDrake, WMAkker, SADruce, MRBackground: 131 I-meta-iodobenzylguanidine (131 I-MIBG) has been in therapeutic use since 1980s. Newer treatment modalities are emerging for neuroendocrine tumours (NETs) and chromaffin cell tumours (CCTs), but many of these do not yet have adequate long-term follow-up to determine their longer term efficacy and sequelae. Methods: Fifty-eight patients with metastatic NETs and CCTs who had received 131 I-MIBG therapy between 2000 and 2011 were analysed. Survival and any long-term haematological or renal sequelae were investigated.Results:In the NET group, the overall median survival and median survival following the diagnosis of metastatic disease was 124 months. The median survival following the commencement of 131 I-MIBG was 66 months. For the CCT group, median survival had not been reached. The 5-year survival from diagnosis and following the diagnosis of metastatic disease was 67% and 67.5% for NETs and CCTs, respectively. The 5-year survival following the commencement of 131 I-MIBG therapy was 68%. Thirty-two patients had long-term haematological sequelae: 5 of these 32 patients developed haematological malignancies. Two patients developed a mild deterioration in renal function. Conclusion: Long follow up of 131 I-MIBG therapy reveals a noteable rate of bone marrow toxicities and malignancy and long term review of all patients receiving radionuclide therapies is recommended. © 2013 Cancer Research UK. All rights reserved. |
| spellingShingle | Sze, W Grossman, AB Goddard, I Amendra, D Shieh, S Plowman, P Drake, WM Akker, SA Druce, MR Sequelae and survivorship in patients treated with 131 I-MIBG therapy |
| title | Sequelae and survivorship in patients treated with 131 I-MIBG therapy |
| title_full | Sequelae and survivorship in patients treated with 131 I-MIBG therapy |
| title_fullStr | Sequelae and survivorship in patients treated with 131 I-MIBG therapy |
| title_full_unstemmed | Sequelae and survivorship in patients treated with 131 I-MIBG therapy |
| title_short | Sequelae and survivorship in patients treated with 131 I-MIBG therapy |
| title_sort | sequelae and survivorship in patients treated with 131 i mibg therapy |
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