Anemia / 2013 / Article

Clinical Study | Open Access

Volume 2013 |Article ID 121762 |

Alexandros Makis, Nikolaos Chaliasos, Sapfo Alfantaki, Paraskevi Karagouni, Antigone Siamopoulou, "Chelation Therapy with Oral Solution of Deferiprone in Transfusional Iron-Overloaded Children with Hemoglobinopathies", Anemia, vol. 2013, Article ID 121762, 3 pages, 2013.

Chelation Therapy with Oral Solution of Deferiprone in Transfusional Iron-Overloaded Children with Hemoglobinopathies

Academic Editor: Eitan Fibach
Received18 Jun 2013
Accepted21 Sep 2013
Published04 Nov 2013


Iron overload in hemoglobinopathies is secondary to blood transfusions, chronic hemolysis, and increased iron absorption and leads to tissue injury requiring the early use of chelating agents. The available agents are parenteral deferoxamine and oral deferiprone and deferasirox. There are limited data on the safety and efficacy of deferiprone at a very young age. The aim of our study was the presentation of data regarding the use of oral solution of deferiprone in 9 children (mean age 6.5, range 2–10) with transfusion dependent hemoglobinopathies (6 beta thalassemia major, 1 thalassemia intermedia, and 2 sickle cell beta thalassemia). The mean duration of treatment was 21.5 months (range 15–31). All children received the oral solution without any problems of compliance. Adverse reactions were temporary abdominal discomfort and diarrhea (1 child), mild neutropenia (1 child) that resolved with no need of discontinuation of treatment, and transient arthralgia (1 child) that resolved spontaneously. The mean ferritin levels were significantly reduced at the end of 12 months (initial 2440 versus final 1420 μg/L, ). This small study shows that oral solution of deferiprone was well tolerated by young children and its use was not associated with major safety concerns. Furthermore, it was effective in decreasing serum ferritin.

1. Introduction

Children with transfusion dependent hemoglobinopathies rapidly develop potentially damaging levels of toxic iron overload in many vital organs. Iron removal with chelating agents is required early in life and in some cases after the age of two [1]. Therefore, the safety, efficacy, and compliance regarding the use of iron chelators are of high significance because of the long-term nature of the treatment. Currently available chelators are deferoxamine, which is administered intravenously or subcutaneously, and the deferasirox and deferiprone that are given orally. The oral administration of iron chelation is most welcome by children with hemoglobinopathies who have problems with the discomfort of deferoxamine injections. Furthermore, early and aggressive chronic administration with deferoxamine can affect many organs and especially skeletal maturation and result in growth retardation [2, 3]. But even more important is deferiprone’s superior ability to protect the heart, which has been shown to improve survival in many studies [4, 5]. Limited clinical data on the safety and efficacy of deferiprone on very young age allow us to add our experience [68].

The aim of our study was the presentation of data regarding the clinical benefit and side effects of liquid oral solution of deferiprone in young children with hemoglobinopathies less than 10 years old.

2. Patients and Methods

The Thalassemia Unit of the Department of Pediatrics at the University Hospital of Ioannina, Ioannina, Greece, is the reference center for children with hemoglobinopathies in northwest Greece and patients regularly attend for investigation, clinical follow-up, and treatment; their information is prospectively recorded. We collected information during the treatment with liquid oral solution of deferiprone (Ferriprox 100 mg/mL) from nine children with transfusion dependent hemoglobinopathies. Six children had beta thalassemia major, 1 thalassemia intermedia, and 2 sickle cell beta thalassemia. The principles outlined in the Declaration of Helsinki had been followed. The diagnosis was based on the clinical, hematological, biosynthetic, and genetic studies. The characteristics of the study group are shown in Table 1. The mean number of red blood cell transfusions during the previous year was 10.6 (range 8–15). All the children had chronic iron overload requiring chelation therapy, as defined by serum ferritin concentration (mean ± standard error (SE): μg/L). The mean age at the beginning of the treatment was 6.5 (range 2–10), five were boys, and four were girls. All the children were naïve to iron chelation therapy before this study, except two patients who were receiving deferoxamine ( ; mean dose = 35 mg/kg/d; mean duration of use = 1.5 years). One child was splenectomized. All the children had negative anti-hepatitis C antibody status at baseline.


Age (years)2–10, mean 6.5
Male : Female5 : 4
-Thalassemia major6
Thalassemia intermedia2
Sickle/β thalassemia1
Red blood cell transfusions during the last yearRange 8–15, mean 10.6
Chelation therapy with deferoxamine before the initiation of the study ; mean dose = 35 mg/kg/d; mean duration of use = 1.5 years
Oral liquid deferiprone dosage 50–100 mg/Kg/d, mean 75.2
Duration of oral liquid deferiprone (months)Range 15–31, mean 21.5

Therapy, with oral solution of deferiprone, was initiated at a daily dose of 50 mg/kg, divided into 3 doses, for the first 2 weeks. The dose was increased to 75 mg/kg, for another 2 weeks. If the patient’s serum ferritin concentration at baseline was greater than 2500 μg/L, the dose was further increased to a total daily dose of 100 mg/kg after 4 weeks of deferiprone therapy. After initiation of the treatment, full blood count was assessed weekly, serum ferritin was assessed monthly, and liver and renal functions were assessed bimonthly. The mean duration of the administration of liquid oral solution of deferiprone was 21.5 months (range 15–31 months). To evaluate the efficacy and safety of deferiprone treatment, biochemical parameters such as serum ferritin and liver enzymes were analyzed using the Student -test. All parameters are presented as mean ± standard error (SE). values less than 0.05 were considered statistically significant.

3. Results and Discussion

The hematological and biochemical markers during treatment are shown in Table 2. All the children received the oral deferiprone without any problems of compliance. The adverse reactions that were noticed during treatment were the following: temporary abdominal discomfort and diarrhea at initiation of therapy that resolved despite continued deferiprone (one child, age 8 years), mild neutropenia (1.2 × 109/L) that resolved within 8 days despite continued deferiprone therapy (one child, age 4 years), and transient arthralgia that resolved spontaneously (one child, age 10). Deferiprone oral solution was effective in reducing serum ferritin (mean ± SE) (initial μg/L versus final μg/L, ) (Figure 1). Five children of the study were <6 years old. The baseline serum ferritin of these children was significantly lower than the children >6 years (2250 μg/L ±880 versus 2950 μg/L ±1550, ). The differences in changes in serum ferritin as well as in other parameters did not reach statistical significance between the two age groups (Table 2).

ParametersTotal<6 years>6 years

White blood cells ( 109/L)
Hemoglobin (g/L)
Platelets ( 109/L)
Creatinine (μmol/L)
Ferritin (μg/L)

Values presented as mean ± SE; .

Deferiprone, previously only in tablet form, is not suitable for young children under the age of six years. Recently the solution form of deferiprone has been introduced. However, the clinical data regarding its use in small children are quite limited. A very recent clinical study of deferiprone on children less than 10 years was conducted in Egypt, Malaysia, and Indonesia [8]. El Alfy and colleagues reviewed the use of liquid oral solution of deferiprone in 100 children (mean age 5.1 years) with thalassemia or sickle cell disease. At the end of the 6-month treatment period, there was a significant drop in mean serum ferritin levels. Therapy was not associated with unexpected adverse reactions, as it was noticed in our study. Similar results were reported in another trial of pediatric patients who received tablet formulation of deferiprone (median age 10.6 years) [7]. Mean serum ferritin levels decreased significantly following a median treatment duration of 11.4 months. The investigators of another study tried to assess the safety of deferiprone in very young children (<6 years). Nausea and vomiting were noticed in 27%, joint symptoms in 9%, and neutropenia in 4.5% of the patients. None of the patients had agranulocytosis. Interestingly, thrombocytopenia was observed in 45% of the patients. Transient interruption of treatment led to reversal of symptoms in the majority of patients [6].

In our study, we examined the clinical benefit and safety of liquid oral solution of deferiprone in young children with transfusion dependent hemoglobinopathies. Although the number of the patients was small, we noticed that deferiprone oral solution was well tolerated and its use was not associated with major safety concerns, while it was effective in decreasing serum ferritin.

In conclusion, assuming the same biological efficacy as the tablet form, deferiprone solution seems to benefit the young children, and they may not require injectable iron chelation. Further studies with large number of patients and long-term follow-up are needed to evaluate the safety and efficacy profile of deferiprone oral solution in small children.


Part of this work was presented at the 53rd Annual Meeting of American Society of Hematology, San Diego, USA, December 12, 2011. The paper has not been published before and is not under consideration in any other journals.

Conflict of Interests

The authors declared that there is no conflict of interests.


  1. C. Hershko, “Pathogenesis and management of iron toxicity in thalassemia,” Annals of the New York Academy of Sciences, vol. 1202, pp. 1–9, 2010. View at: Publisher Site | Google Scholar
  2. N. F. Olivieri, J. R. Buncic, and E. Chew, “Visual and auditory neurotoxicity in patients receiving subcutaneous deferoxamine infusions,” The New England Journal of Medicine, vol. 314, no. 14, pp. 869–873, 1986. View at: Google Scholar
  3. S. De Virgiliis, M. Congia, F. Frau et al., “Deferoxamine-induced growth retardation in patients with thalassemia major,” Journal of Pediatrics, vol. 113, no. 4, pp. 661–669, 1988. View at: Google Scholar
  4. D. J. Pennell, V. Berdoukas, M. Karagiorga et al., “Randomized controlled trial of deferiprone or deferoxamine in beta-thalassemia major patients with asymptomatic myocardial siderosis,” Blood, vol. 107, no. 9, pp. 3738–3744, 2006. View at: Publisher Site | Google Scholar
  5. M. A. Tanner, R. Galanello, C. Dessi et al., “A randomized, placebo-controlled, double-blind trial of the effect of combined therapy with deferoxamine and deferiprone on myocardial iron in thalassemia major using cardiovascular magnetic resonance,” Circulation, vol. 115, no. 14, pp. 1876–1884, 2007. View at: Publisher Site | Google Scholar
  6. R. Naithani, J. Chandra, and S. Sharma, “Safety of oral iron chelator deferiprone in young thalassaemics,” European Journal of Haematology, vol. 74, no. 3, pp. 217–220, 2005. View at: Publisher Site | Google Scholar
  7. S. C. Won, D. K. Han, J. J. Seo et al., “Efficacy and safety of deferiprone (Ferriprox), an oral iron-chelating agent, in pediatric patients,” Korean Journal of Hematology, vol. 45, pp. 58–61, 2010. View at: Google Scholar
  8. M. El Alfy, T. T. Sari, C. L. Lee, F. Tricta, and A. El-Beshlawy, “The safety, tolerability, and efficacy of a liquid formulation of deferiprone in young children with transfusional iron overload,” Journal of Pediatric Hematology/Oncology, vol. 32, no. 8, pp. 601–605, 2010. View at: Publisher Site | Google Scholar

Copyright © 2013 Alexandros Makis et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

1760 Views | 869 Downloads | 6 Citations
 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

We are committed to sharing findings related to COVID-19 as quickly as possible. We will be providing unlimited waivers of publication charges for accepted research articles as well as case reports and case series related to COVID-19. Review articles are excluded from this waiver policy. Sign up here as a reviewer to help fast-track new submissions.