Oxaliplatin-related thrombocytopenia
Main Author: | |
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Publication Date: | 2012 |
Other Authors: | , , , |
Format: | Article |
Language: | eng |
Source: | Repositório Institucional da UNIFESP |
Download full: | http://dx.doi.org/10.1093/annonc/mds074 http://repositorio.unifesp.br/handle/11600/35102 |
Summary: | Oxaliplatin is a third generation platinum compound that inhibits DNA synthesis, mainly through intrastrandal cross-links in DNA. Most of the experience with the clinical use of this drug is derived from colorectal cancer but it is also used in other tumor types such as ovary, breast, liver and non-Hodgkin's lymphoma. Thrombocytopenia is a frequent toxicity seen during oxaliplatin treatment, occurring at any grade in up to 70 % of patients and leading to delays or even discontinuation of the chemotherapy. Although myelossupression is recognized as the main cause of oxaliplatin-related thrombocytopenia, new mechanisms for this side-effect have emerged, including splenic sequestration of platelets related to oxaliplatin-induced liver damage and immune thrombocytopenia. These new pathophysiology pathways have different clinical presentations and evolution and may need specific therapeutic maneuvers. This article attempts to review this topic and provides useful clinical information for the management of oxaliplatin-related thrombocytopenia. |
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Oxaliplatin-related thrombocytopeniamyelossupressionoxaliplatinreviewthrombocytopeniaOxaliplatin is a third generation platinum compound that inhibits DNA synthesis, mainly through intrastrandal cross-links in DNA. Most of the experience with the clinical use of this drug is derived from colorectal cancer but it is also used in other tumor types such as ovary, breast, liver and non-Hodgkin's lymphoma. Thrombocytopenia is a frequent toxicity seen during oxaliplatin treatment, occurring at any grade in up to 70 % of patients and leading to delays or even discontinuation of the chemotherapy. Although myelossupression is recognized as the main cause of oxaliplatin-related thrombocytopenia, new mechanisms for this side-effect have emerged, including splenic sequestration of platelets related to oxaliplatin-induced liver damage and immune thrombocytopenia. These new pathophysiology pathways have different clinical presentations and evolution and may need specific therapeutic maneuvers. This article attempts to review this topic and provides useful clinical information for the management of oxaliplatin-related thrombocytopenia.Hosp Sirio Libanes, Dept Clin Oncol, BR-01308050 São Paulo, BrazilUniv Fed Estado São Paulo, Dept Clin & Expt Hematol, São Paulo, BrazilUniv São Paulo, Fac Med, Inst Canc Estado São Paulo, Dept Radiol & Oncol, São Paulo, BrazilUniv Fed Estado São Paulo, Dept Clin & Expt Hematol, São Paulo, BrazilWeb of ScienceOxford Univ PressHosp Sirio LibanesUniversidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Jardim, D. L.Rodrigues, C. A. [UNIFESP]Novis, Y. A. S.Rocha, V. G.Hoff, P. M.2016-01-24T14:27:29Z2016-01-24T14:27:29Z2012-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1937-1942http://dx.doi.org/10.1093/annonc/mds074Annals of Oncology. Oxford: Oxford Univ Press, v. 23, n. 8, p. 1937-1942, 2012.10.1093/annonc/mds0740923-7534http://repositorio.unifesp.br/handle/11600/35102WOS:000306924400004engAnnals of Oncologyinfo:eu-repo/semantics/openAccesshttp://www.oxfordjournals.org/access_purchase/self-archiving_policyb.htmlreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2023-03-27T12:03:15Zoai:repositorio.unifesp.br/:11600/35102Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652023-03-27T12:03:15Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Oxaliplatin-related thrombocytopenia |
title |
Oxaliplatin-related thrombocytopenia |
spellingShingle |
Oxaliplatin-related thrombocytopenia Jardim, D. L. myelossupression oxaliplatin review thrombocytopenia |
title_short |
Oxaliplatin-related thrombocytopenia |
title_full |
Oxaliplatin-related thrombocytopenia |
title_fullStr |
Oxaliplatin-related thrombocytopenia |
title_full_unstemmed |
Oxaliplatin-related thrombocytopenia |
title_sort |
Oxaliplatin-related thrombocytopenia |
author |
Jardim, D. L. |
author_facet |
Jardim, D. L. Rodrigues, C. A. [UNIFESP] Novis, Y. A. S. Rocha, V. G. Hoff, P. M. |
author_role |
author |
author2 |
Rodrigues, C. A. [UNIFESP] Novis, Y. A. S. Rocha, V. G. Hoff, P. M. |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Hosp Sirio Libanes Universidade Federal de São Paulo (UNIFESP) Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Jardim, D. L. Rodrigues, C. A. [UNIFESP] Novis, Y. A. S. Rocha, V. G. Hoff, P. M. |
dc.subject.por.fl_str_mv |
myelossupression oxaliplatin review thrombocytopenia |
topic |
myelossupression oxaliplatin review thrombocytopenia |
description |
Oxaliplatin is a third generation platinum compound that inhibits DNA synthesis, mainly through intrastrandal cross-links in DNA. Most of the experience with the clinical use of this drug is derived from colorectal cancer but it is also used in other tumor types such as ovary, breast, liver and non-Hodgkin's lymphoma. Thrombocytopenia is a frequent toxicity seen during oxaliplatin treatment, occurring at any grade in up to 70 % of patients and leading to delays or even discontinuation of the chemotherapy. Although myelossupression is recognized as the main cause of oxaliplatin-related thrombocytopenia, new mechanisms for this side-effect have emerged, including splenic sequestration of platelets related to oxaliplatin-induced liver damage and immune thrombocytopenia. These new pathophysiology pathways have different clinical presentations and evolution and may need specific therapeutic maneuvers. This article attempts to review this topic and provides useful clinical information for the management of oxaliplatin-related thrombocytopenia. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-08-01 2016-01-24T14:27:29Z 2016-01-24T14:27:29Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1093/annonc/mds074 Annals of Oncology. Oxford: Oxford Univ Press, v. 23, n. 8, p. 1937-1942, 2012. 10.1093/annonc/mds074 0923-7534 http://repositorio.unifesp.br/handle/11600/35102 WOS:000306924400004 |
url |
http://dx.doi.org/10.1093/annonc/mds074 http://repositorio.unifesp.br/handle/11600/35102 |
identifier_str_mv |
Annals of Oncology. Oxford: Oxford Univ Press, v. 23, n. 8, p. 1937-1942, 2012. 10.1093/annonc/mds074 0923-7534 WOS:000306924400004 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Annals of Oncology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess http://www.oxfordjournals.org/access_purchase/self-archiving_policyb.html |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://www.oxfordjournals.org/access_purchase/self-archiving_policyb.html |
dc.format.none.fl_str_mv |
1937-1942 |
dc.publisher.none.fl_str_mv |
Oxford Univ Press |
publisher.none.fl_str_mv |
Oxford Univ Press |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1841453720977539072 |