Literature DB >> 10519721

Preliminary report of a toxicity study of hydroxyurea in sickle cell disease. French Study Group on Sickle Cell Disease.

M de Montalembert1, P Bégué, F Bernaudin, I Thuret, D Bachir, M Micheau.   

Abstract

AIM: To evaluate the tolerance of hydroxyurea in children affected with sickle cell disease.
DESIGN: Questionnaire study of French physicians likely to treat patients with sickle cell disease. Data were collected on 101 children with sickle cell disease, treated for a median of 22 months, 36 of whom were treated for more than three years. 13 children were younger than 5 years of age at inclusion.
RESULTS: Hydroxyurea was stopped for medical reasons in 11 patients: 6 failures, 1 pregnancy, 1 cutaneous rash, 1 leg ulcer, 1 lupus. Acute lymphoblastic leukaemia occurred in a girl treated for 1.5 months with hydroxyurea, this short interval arguing against a causative association. One 17 year old boy had paraparesis after 8 years of treatment.
CONCLUSIONS: No major short or medium term toxicity was related to hydroxyurea in this cohort of 101 children. However, the number of children treated for more than 3 years is too few to make firm conclusions on the long term tolerance of this drug.

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Year:  1999        PMID: 10519721      PMCID: PMC1718114          DOI: 10.1136/adc.81.5.437

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  13 in total

1.  Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. The French Study Group on Sickle Cell Disease.

Authors:  M de Montalembert; M Belloy; F Bernaudin; F Gouraud; R Capdeville; R Mardini; N Philippe; J P Jais; J Bardakdjian; R Ducrocq; M Maier-Redelsperger; J Elion; D Labie; R Girot
Journal:  J Pediatr Hematol Oncol       Date:  1997 Jul-Aug       Impact factor: 1.289

2.  Treatment of polycythemia vera: the use of hydroxyurea and pipobroman in 292 patients under the age of 65 years.

Authors:  Y Najean; J D Rain
Journal:  Blood       Date:  1997-11-01       Impact factor: 22.113

Review 3.  Use of hydroxyurea in children with sickle cell disease: what comes next?

Authors:  K Ohene-Frempong; K Smith-Whitley
Journal:  Semin Hematol       Date:  1997-07       Impact factor: 3.851

4.  Bone marrow transplantation for sickle cell disease.

Authors:  M C Walters; M Patience; W Leisenring; J R Eckman; J P Scott; W C Mentzer; S C Davies; K Ohene-Frempong; F Bernaudin; D C Matthews; R Storb; K M Sullivan
Journal:  N Engl J Med       Date:  1996-08-08       Impact factor: 91.245

5.  Hydroxyurea therapy in children severely affected with sickle cell disease.

Authors:  J P Scott; C A Hillery; E R Brown; V Misiewicz; R J Labotka
Journal:  J Pediatr       Date:  1996-06       Impact factor: 4.406

6.  Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial.

Authors:  A Ferster; C Vermylen; G Cornu; M Buyse; F Corazza; C Devalck; P Fondu; M Toppet; E Sariban
Journal:  Blood       Date:  1996-09-15       Impact factor: 22.113

7.  Clinical and hematologic effects of hydroxyurea in children with sickle cell anemia.

Authors:  S Jayabose; O Tugal; C Sandoval; P Patel; D Puder; T Lin; P Visintainer
Journal:  J Pediatr       Date:  1996-10       Impact factor: 4.406

8.  A cautionary note regarding hydroxyurea in sickle cell disease.

Authors:  E P Vichinsky; B H Lubin
Journal:  Blood       Date:  1994-02-15       Impact factor: 22.113

9.  Fetal haemoglobin variations following hydroxyurea treatment in patients with cyanotic congenital heart disease.

Authors:  P Triadou; M Maier-Redelsperger; R Krishnamoorty; A Deschamps; N Casadevall; O Dunda; R Ducrocq; J Elion; R Girot; D Labie
Journal:  Nouv Rev Fr Hematol       Date:  1994-10

10.  Anticoagulant effects of 1alpha,25-dihydroxyvitamin D3 on human myelogenous leukemia cells and monocytes.

Authors:  T Koyama; M Shibakura; M Ohsawa; R Kamiyama; S Hirosawa
Journal:  Blood       Date:  1998-07-01       Impact factor: 22.113

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  11 in total

1.  Occurrence of acute myeloid leukemia in hydroxyurea-treated sickle cell disease patient.

Authors:  Samuel Regan; Xuebin Yang; Niklas K Finnberg; Wafik S El-Deiry; Jeffrey J Pu
Journal:  Cancer Biol Ther       Date:  2019-08-18       Impact factor: 4.742

2.  Genotype-phenotype relationship of patients with β-thalassemia taking hydroxyurea: a 13-year experience in Iran.

Authors:  Mehran Karimi; Sezaneh Haghpanah; Ali Farhadi; Majid Yavarian
Journal:  Int J Hematol       Date:  2011-12-20       Impact factor: 2.490

Review 3.  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 4.  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 5.  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

Review 6.  Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease.

Authors:  Sophie Lanzkron; John J Strouse; Renee Wilson; Mary Catherine Beach; Carlton Haywood; HaeSong Park; Catherine Witkop; Eric B Bass; Jodi B Segal
Journal:  Ann Intern Med       Date:  2008-05-05       Impact factor: 25.391

7.  Myelosuppression in patients benefiting from imatinib with hydroxyurea for recurrent malignant gliomas.

Authors:  Gaurav D Shah; Joel S Silver; Steven S Rosenfeld; Igor T Gavrilovic; Lauren E Abrey; Andrew B Lassman
Journal:  J Neurooncol       Date:  2007-06-27       Impact factor: 4.130

8.  Myocardial ischaemia in children with sickle cell disease.

Authors:  M de Montalembert; C Maunoury; P Acar; V Brousse; D Sidi; G Lenoir
Journal:  Arch Dis Child       Date:  2004-04       Impact factor: 3.791

9.  Development of myelodysplastic syndrome and acute myeloid leukemia 15 years after hydroxyurea use in a patient with sickle cell anemia.

Authors:  Walid Baz; Vesna Najfeld; Matthew Yotsuya; Jotica Talwar; Terenig Terjanian; Frank Forte
Journal:  Clin Med Insights Oncol       Date:  2012-03-07

Review 10.  [From Hemoglobin SS to SF: interest of hydroxyurea in the management of sickle cell disease in two Congolese children and review of the literature].

Authors:  Gayllord Mutoke Nkashama; Gray Kanteng A Wakamb; Augustin Mutombo Mulangu; Georges Mutoke Nkashama; Boniface Kabeya Kupa; Oscar Luboya Numbi
Journal:  Pan Afr Med J       Date:  2015-06-15
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