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(32)P in the treatment of myeloproliferative disorders
(32)P has been available for the treatment of myeloproliferative neoplasms (MPNs) for over seventy years. It was first used in 1938 by John H Lawrence in the treatment of polycythaemia and chronic leukaemias. With the introduction of agents such as hydroxycarbamide, interferon and anagrelide the rol...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Ulster Medical Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920483/ https://www.ncbi.nlm.nih.gov/pubmed/27601760 |
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author | Lawless, Sarah McMullin, Mary Frances Cuthbert, Robert Houston, Russell |
author_facet | Lawless, Sarah McMullin, Mary Frances Cuthbert, Robert Houston, Russell |
author_sort | Lawless, Sarah |
collection | PubMed |
description | (32)P has been available for the treatment of myeloproliferative neoplasms (MPNs) for over seventy years. It was first used in 1938 by John H Lawrence in the treatment of polycythaemia and chronic leukaemias. With the introduction of agents such as hydroxycarbamide, interferon and anagrelide the role of (32)P has been diminished. Today, Polycythaemia Rubra Vera (PRV) and Essential Thrombocythaemia (ET) remain the only myeloproliferative conditions in which (32)P is indicated. MATERIALS AND METHODS: We carried out a retrospective review of all patients who had received 32P in Northern Ireland over a 24 year period. The time to successful response, duration of response, and associated complications were reviewed. RESULTS: (32)P was successful in inducing remission in 90% of patients. This remission was sustained following one dose without the need for further therapy in 37% of cases. 47% required repeated doses. 26% required recommencement of alternative therapies. No cases of thrombosis, myelofibrosis or acute leukaemia were observed. DISCUSSION: We conclude that (32)P is a well-tolerated and efficacious treatment option in the elderly. We discuss our results compared with previous work in this area. (32)P will continue to be offered to elderly patients in our practice. |
format | Online Article Text |
id | pubmed-4920483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Ulster Medical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-49204832016-09-06 (32)P in the treatment of myeloproliferative disorders Lawless, Sarah McMullin, Mary Frances Cuthbert, Robert Houston, Russell Ulster Med J Clinical Paper (32)P has been available for the treatment of myeloproliferative neoplasms (MPNs) for over seventy years. It was first used in 1938 by John H Lawrence in the treatment of polycythaemia and chronic leukaemias. With the introduction of agents such as hydroxycarbamide, interferon and anagrelide the role of (32)P has been diminished. Today, Polycythaemia Rubra Vera (PRV) and Essential Thrombocythaemia (ET) remain the only myeloproliferative conditions in which (32)P is indicated. MATERIALS AND METHODS: We carried out a retrospective review of all patients who had received 32P in Northern Ireland over a 24 year period. The time to successful response, duration of response, and associated complications were reviewed. RESULTS: (32)P was successful in inducing remission in 90% of patients. This remission was sustained following one dose without the need for further therapy in 37% of cases. 47% required repeated doses. 26% required recommencement of alternative therapies. No cases of thrombosis, myelofibrosis or acute leukaemia were observed. DISCUSSION: We conclude that (32)P is a well-tolerated and efficacious treatment option in the elderly. We discuss our results compared with previous work in this area. (32)P will continue to be offered to elderly patients in our practice. The Ulster Medical Society 2016-05 /pmc/articles/PMC4920483/ /pubmed/27601760 Text en © The Ulster Medical Society, 2016 |
spellingShingle | Clinical Paper Lawless, Sarah McMullin, Mary Frances Cuthbert, Robert Houston, Russell (32)P in the treatment of myeloproliferative disorders |
title | (32)P in the treatment of myeloproliferative disorders |
title_full | (32)P in the treatment of myeloproliferative disorders |
title_fullStr | (32)P in the treatment of myeloproliferative disorders |
title_full_unstemmed | (32)P in the treatment of myeloproliferative disorders |
title_short | (32)P in the treatment of myeloproliferative disorders |
title_sort | (32)p in the treatment of myeloproliferative disorders |
topic | Clinical Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920483/ https://www.ncbi.nlm.nih.gov/pubmed/27601760 |
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