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Temozolomide in aggressive pituitary adenomas and carcinomas
Temozolomide is an alkylating agent used in the treatment of gliomas and, more recently, aggressive pituitary adenomas and carcinomas. Temozolomide methylates DNA and, thereby, has antitumor effects. O(6)-methylguanine-DNA methyltransferase, a DNA repair enzyme, removes the alkylating adducts that a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328813/ https://www.ncbi.nlm.nih.gov/pubmed/22584716 http://dx.doi.org/10.6061/clinics/2012(Sup01)20 |
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author | Ortiz, Leon D. Syro, Luis V. Scheithauer, Bernd W. Rotondo, Fabio Uribe, Humberto Fadul, Camilo E. Horvath, Eva Kovacs, Kalman |
author_facet | Ortiz, Leon D. Syro, Luis V. Scheithauer, Bernd W. Rotondo, Fabio Uribe, Humberto Fadul, Camilo E. Horvath, Eva Kovacs, Kalman |
author_sort | Ortiz, Leon D. |
collection | PubMed |
description | Temozolomide is an alkylating agent used in the treatment of gliomas and, more recently, aggressive pituitary adenomas and carcinomas. Temozolomide methylates DNA and, thereby, has antitumor effects. O(6)-methylguanine-DNA methyltransferase, a DNA repair enzyme, removes the alkylating adducts that are induced by temozolomide, thereby counteracting its effects. A Medline search for all of the available publications regarding the use of temozolomide for the treatment of pituitary tumors was performed. To date, 46 cases of adenohypophysial tumors that were treated with temozolomide, including 30 adenomas and 16 carcinomas, have been reported. Eighteen of the 30 (60%) adenomas and 11 of the 16 (69%) carcinomas responded favorably to treatment. One patient with multiple endocrine neoplasia type 1 and an aggressive prolactin-producing adenoma was also treated and demonstrated a good response. No significant complications have been attributed to temozolomide therapy. Thus, temozolomide is an effective treatment for the majority of aggressive adenomas and carcinomas. Evidence indicates that there is an inverse correlation between levels of O(6)-methylguanine-DNA methyltransferase immunoexpression and therapeutic response. Alternatively, high-level O(6)-methylguanine-DNA methyltransferase immunoexpression correlates with an unfavorable response. Here, we review the use of temozolomide for treating pituitary neoplasms. |
format | Online Article Text |
id | pubmed-3328813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-33288132012-04-19 Temozolomide in aggressive pituitary adenomas and carcinomas Ortiz, Leon D. Syro, Luis V. Scheithauer, Bernd W. Rotondo, Fabio Uribe, Humberto Fadul, Camilo E. Horvath, Eva Kovacs, Kalman Clinics (Sao Paulo) Review Temozolomide is an alkylating agent used in the treatment of gliomas and, more recently, aggressive pituitary adenomas and carcinomas. Temozolomide methylates DNA and, thereby, has antitumor effects. O(6)-methylguanine-DNA methyltransferase, a DNA repair enzyme, removes the alkylating adducts that are induced by temozolomide, thereby counteracting its effects. A Medline search for all of the available publications regarding the use of temozolomide for the treatment of pituitary tumors was performed. To date, 46 cases of adenohypophysial tumors that were treated with temozolomide, including 30 adenomas and 16 carcinomas, have been reported. Eighteen of the 30 (60%) adenomas and 11 of the 16 (69%) carcinomas responded favorably to treatment. One patient with multiple endocrine neoplasia type 1 and an aggressive prolactin-producing adenoma was also treated and demonstrated a good response. No significant complications have been attributed to temozolomide therapy. Thus, temozolomide is an effective treatment for the majority of aggressive adenomas and carcinomas. Evidence indicates that there is an inverse correlation between levels of O(6)-methylguanine-DNA methyltransferase immunoexpression and therapeutic response. Alternatively, high-level O(6)-methylguanine-DNA methyltransferase immunoexpression correlates with an unfavorable response. Here, we review the use of temozolomide for treating pituitary neoplasms. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2012-04 /pmc/articles/PMC3328813/ /pubmed/22584716 http://dx.doi.org/10.6061/clinics/2012(Sup01)20 Text en Copyright © 2012 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Ortiz, Leon D. Syro, Luis V. Scheithauer, Bernd W. Rotondo, Fabio Uribe, Humberto Fadul, Camilo E. Horvath, Eva Kovacs, Kalman Temozolomide in aggressive pituitary adenomas and carcinomas |
title | Temozolomide in aggressive pituitary adenomas and carcinomas |
title_full | Temozolomide in aggressive pituitary adenomas and carcinomas |
title_fullStr | Temozolomide in aggressive pituitary adenomas and carcinomas |
title_full_unstemmed | Temozolomide in aggressive pituitary adenomas and carcinomas |
title_short | Temozolomide in aggressive pituitary adenomas and carcinomas |
title_sort | temozolomide in aggressive pituitary adenomas and carcinomas |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328813/ https://www.ncbi.nlm.nih.gov/pubmed/22584716 http://dx.doi.org/10.6061/clinics/2012(Sup01)20 |
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