Temozolomide in aggressive pituitary adenomas and carcinomas
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/19731 |
Resumo: | 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. O6-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 O6-methylguanine-DNA methyltransferase immunoexpression and therapeutic response. Alternatively, high-level O6-methylguanine-DNA methyltransferase immunoexpression correlates with an unfavorable response. Here, we review the use of temozolomide for treating pituitary neoplasms. |
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Temozolomide in aggressive pituitary adenomas and carcinomasPituitary adenomaPituitary carcinomaMGMTTemozolomideReviewTemozolomide 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. O6-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 O6-methylguanine-DNA methyltransferase immunoexpression and therapeutic response. Alternatively, high-level O6-methylguanine-DNA methyltransferase immunoexpression correlates with an unfavorable response. Here, we review the use of temozolomide for treating pituitary neoplasms.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2012-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/1973110.6061/clinics/2012(Sup01)20Clinics; Vol. 67 No. supl.1 (2012); 119-123Clinics; v. 67 n. supl.1 (2012); 119-123Clinics; Vol. 67 Núm. supl.1 (2012); 119-1231980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/19731/21795Ortiz, Leon D.Syro, Luis V.Scheithauer, Bernd W.Rotondo, FabioUribe, HumbertoFadul, Camilo E.Horvath, EvaKovacs, Kalmaninfo:eu-repo/semantics/openAccess2012-05-24T20:34:37Zoai:revistas.usp.br:article/19731Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-24T20:34:37Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Temozolomide in aggressive pituitary adenomas and carcinomas |
title |
Temozolomide in aggressive pituitary adenomas and carcinomas |
spellingShingle |
Temozolomide in aggressive pituitary adenomas and carcinomas Ortiz, Leon D. Pituitary adenoma Pituitary carcinoma MGMT Temozolomide Review |
title_short |
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_sort |
Temozolomide in aggressive pituitary adenomas and carcinomas |
author |
Ortiz, Leon D. |
author_facet |
Ortiz, Leon D. Syro, Luis V. Scheithauer, Bernd W. Rotondo, Fabio Uribe, Humberto Fadul, Camilo E. Horvath, Eva Kovacs, Kalman |
author_role |
author |
author2 |
Syro, Luis V. Scheithauer, Bernd W. Rotondo, Fabio Uribe, Humberto Fadul, Camilo E. Horvath, Eva Kovacs, Kalman |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Ortiz, Leon D. Syro, Luis V. Scheithauer, Bernd W. Rotondo, Fabio Uribe, Humberto Fadul, Camilo E. Horvath, Eva Kovacs, Kalman |
dc.subject.por.fl_str_mv |
Pituitary adenoma Pituitary carcinoma MGMT Temozolomide Review |
topic |
Pituitary adenoma Pituitary carcinoma MGMT Temozolomide Review |
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. O6-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 O6-methylguanine-DNA methyltransferase immunoexpression and therapeutic response. Alternatively, high-level O6-methylguanine-DNA methyltransferase immunoexpression correlates with an unfavorable response. Here, we review the use of temozolomide for treating pituitary neoplasms. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/19731 10.6061/clinics/2012(Sup01)20 |
url |
https://www.revistas.usp.br/clinics/article/view/19731 |
identifier_str_mv |
10.6061/clinics/2012(Sup01)20 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/19731/21795 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 67 No. supl.1 (2012); 119-123 Clinics; v. 67 n. supl.1 (2012); 119-123 Clinics; Vol. 67 Núm. supl.1 (2012); 119-123 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1824324343818092544 |