Literature DB >> 16550342

Cytotoxic and genotoxic monitoring of sickle cell anaemia patients treated with hydroxyurea.

A S Khayat1, L M Antunes, A C Guimarães, M O Bahia, J A R Lemos, I R Cabral, P D L Lima, M I M Amorim, P C S Cardoso, M A C Smith, R A Santos, R R Burbano.   

Abstract

Very satisfactory results have been obtained with the treatment of sickle cell anaemia with hydroxyurea (HU), an antineoplastic drug. This is because it significantly increases the levels of foetal haemoglobin. Nevertheless, inadequate dosages or prolonged treatment with this pharmaceutical can provoke cytotoxicity or genotoxicity, increasing the risk of neoplasia. We monitored patients under treatment with HU for possible mutagenic effects, through cytogenetic tests (mitotic index and chromosome aberrations) for one year. Checking at two-month intervals, the cytotoxic effect was not evident. There was no evidence of genotoxicity under the conditions of our experiment. However individuals treated with HU should be constantly monitored, as an absence of genotoxicity could be transitory; the mitotic index should also be observed, as an indicator of cytotoxicity.

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Year:  2006        PMID: 16550342     DOI: 10.1007/s10238-006-0091-x

Source DB:  PubMed          Journal:  Clin Exp Med        ISSN: 1591-8890            Impact factor:   3.984


  8 in total

1.  Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: results from the BABY-HUG Phase III Clinical Trial.

Authors:  Patrick T McGann; Jonathan M Flanagan; Thad A Howard; Stephen D Dertinger; Jin He; Anita S Kulharya; Bruce W Thompson; Russell E Ware
Journal:  Pediatr Blood Cancer       Date:  2011-10-19       Impact factor: 3.167

Review 2.  Improving outcomes in children with sickle cell disease: treatment considerations and strategies.

Authors:  Ali Amid; Isaac Odame
Journal:  Paediatr Drugs       Date:  2014-08       Impact factor: 3.022

Review 3.  Novel insights in the management of sickle cell disease in childhood.

Authors:  Lorenzo Iughetti; Elena Bigi; Donatella Venturelli
Journal:  World J Clin Pediatr       Date:  2016-02-08

Review 4.  How I use hydroxyurea to treat young patients with sickle cell anemia.

Authors:  Russell E Ware
Journal:  Blood       Date:  2010-03-11       Impact factor: 22.113

5.  Chromosome damage and repair in children with sickle cell anaemia and long-term hydroxycarbamide exposure.

Authors:  Patrick T McGann; Thad A Howard; Jonathan M Flanagan; Jill M Lahti; Russell E Ware
Journal:  Br J Haematol       Date:  2011-05-04       Impact factor: 6.998

6.  Sensitivity to cisplatin-induced mutations and elevated chromosomal aberrations in lymphocytes from sickle cell disease patients.

Authors:  Polyanna Miranda Alves; Paulo Roberto Juliano Martins; Francisca da Luz Dias; Rommel Mario Rodríguez Burbano; Maria de Lourdes Pires Bianchi; Lusânia Maria Greggi Antunes
Journal:  Clin Exp Med       Date:  2008-04-03       Impact factor: 3.984

7.  From infancy to adolescence: fifteen years of continuous treatment with hydroxyurea in sickle cell anemia.

Authors:  Jane S Hankins; Banu Aygun; Kerri Nottage; Courtney Thornburg; Matthew P Smeltzer; Russell E Ware; Winfred C Wang
Journal:  Medicine (Baltimore)       Date:  2014-12       Impact factor: 1.889

8.  Evaluation of hydroxyurea genotoxicity in patients with sickle cell disease.

Authors:  Emanuel Almeida Moreira de Oliveira; Kenia de Assis Boy; Ana Paula Pinho Santos; Carla da Silva Machado; Cibele Velloso-Rodrigues; Pâmela Souza Almeida Silva Gerheim; Leonardo Meneghin Mendonça
Journal:  Einstein (Sao Paulo)       Date:  2019-09-09
  8 in total

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