Literature DB >> 12100170

The safety and effectiveness of deferiprone in a large-scale, 3-year study in Italian patients.

Adriana Ceci1, Paola Baiardi, Mariagrazia Felisi, Maria Domenica Cappellini, Vittorio Carnelli, Vincenzo De Sanctis, Renzo Galanello, Aurelio Maggio, Giuseppe Masera, Antonio Piga, Francesco Schettini, Ippazio Stefàno, Fernando Tricta.   

Abstract

In 1997, the Italian Ministry of Health created a special programme for the controlled distribution of deferiprone to collect data and to evaluate its safety and effectiveness in long-term use. Five hundred and thirty-two thalassaemia patients from 86 treatment centres were enrolled in this programme. One hundred and eighty-seven patients (32%) experienced a total of 269 events that led to a temporary interruption or, in some cases, to a discontinuation of treatment. The incidence of agranulocytosis and milder neutropenias were 0.4/100 and 2.1/100 patient-years respectively. Neutropenia occurred predominantly in younger and non-splenectomized patients. Transient alanine transaminase increase, gastrointestinal discomfort and arthralgia were the other most commonly reported events. Ferritin levels showed a significant decrease in time after 3 years of therapy. This is the largest number of deferiprone-treated patients to have been reported to date. These data show that the drug was effective in reducing serum ferritin levels and the incidence of adverse events was not greater than the frequency reported in clinical trials.

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Year:  2002        PMID: 12100170     DOI: 10.1046/j.1365-2141.2002.03554.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  36 in total

1.  Agranulocytosis due to deferiprone: a case report with cytomorphological and functional bone marrow examination.

Authors:  Nicoletta Masera; Luisa Tavecchia; Daniela Valentina Longoni; Oscar Maglia; Andrea Biondi; Giuseppe Masera
Journal:  Blood Transfus       Date:  2011-07-18       Impact factor: 3.443

2.  Community-acquired meningitis and sepsis caused by Chryseobacterium meningosepticum in a patient diagnosed with thalassemia major.

Authors:  Nisel Ozkalay; Murat Anil; Neval Agus; Mehmet Helvaci; Seral Sirti
Journal:  J Clin Microbiol       Date:  2006-08       Impact factor: 5.948

Review 3.  Deferasirox for managing iron overload in people with thalassaemia.

Authors:  Claudia Bollig; Lisa K Schell; Gerta Rücker; Roman Allert; Edith Motschall; Charlotte M Niemeyer; Dirk Bassler; Joerg J Meerpohl
Journal:  Cochrane Database Syst Rev       Date:  2017-08-15

Review 4.  Deferasirox for managing iron overload in people with myelodysplastic syndrome.

Authors:  Joerg J Meerpohl; Lisa K Schell; Gerta Rücker; Nigel Fleeman; Edith Motschall; Charlotte M Niemeyer; Dirk Bassler
Journal:  Cochrane Database Syst Rev       Date:  2014-10-28

5.  Long-term safety of deferiprone treatment in children from the Mediterranean region with beta-thalassemia major: the DEEP-3 multi-center observational safety study.

Authors:  Sebastian Botzenhardt; Mariagrazia Felisi; Donato Bonifazi; Giovanni C Del Vecchio; Maria C Putti; Antonis Kattamis; Adriana Ceci; Ian C K Wong; Antje Neubert
Journal:  Haematologica       Date:  2017-10-27       Impact factor: 9.941

6.  Safety and efficacy of iron chelation therapy with deferiprone in patients with transfusion-dependent thalassemia.

Authors:  Saumya S Jamuar; Angeline H M Lai
Journal:  Ther Adv Hematol       Date:  2012-10

7.  Iron overload in patients undergoing hematopoietic stem cell transplantation.

Authors:  Vinod Pullarkat
Journal:  Adv Hematol       Date:  2010-09-08

8.  Efficacy and safety of deferiprone (Ferriprox), an oral iron-chelating agent, in pediatric patients.

Authors:  Sung Chul Won; Dong Kyun Han; Jong Jin Seo; Nak Gyun Chung; Sang Kyu Park; Kyung Bae Park; Hoon Kook; Chuhl Joo Lyu
Journal:  Korean J Hematol       Date:  2010-03-31

9.  Update on the use of deferasirox in the management of iron overload.

Authors:  Ali Taher; Maria Domenica Cappellini
Journal:  Ther Clin Risk Manag       Date:  2009-11-02       Impact factor: 2.423

10.  Can homeopathy bring additional benefits to thalassemic patients on hydroxyurea therapy? Encouraging results of a preliminary study.

Authors:  Antara Banerjee; Sudipa Basu Chakrabarty; Susanta Roy Karmakar; Amit Chakrabarty; Surjyo Jyoti Biswas; Saiful Haque; Debarsi Das; Saili Paul; Biswapati Mandal; Boujedaini Naoual; Philippe Belon; Anisur Rahman Khuda-Bukhsh
Journal:  Evid Based Complement Alternat Med       Date:  2007-10-29       Impact factor: 2.629

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