CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2017; 38(02): 103-110
DOI: 10.4103/ijmpo.ijmpo_103_16
Original Article

Efficacy and Safety of Deferasirox in Pediatric Patients of Thalassemia at a Tertiary Care Teaching Hospital

Dhaval R Thakor
Department of Pharmacology, Civil Hospital, B. J. Medical College, Ahmedabad, Gujarat, India
,
Chetna K Desai
Department of Pharmacology, Civil Hospital, B. J. Medical College, Ahmedabad, Gujarat, India
,
Jigar D Kapadia
Department of Pharmacology, Civil Hospital, B. J. Medical College, Ahmedabad, Gujarat, India
,
Ram K Dikshit
Department of Pharmacology, GCS Medical College and Hospital, Ahmedabad, Gujarat, India
,
KM Mehariya
Department of Paediatrics, Civil Hospital, Ahmedabad, Gujarat, India
› Author Affiliations
Financial support and sponsorship Nil.

Abstract

Objective: To evaluate efficacy, safety and utilization pattern of deferasirox in paediatric patients of transfusion dependant β Thalassemia Major at a tertiary care teaching hospital in Gujarat. Materials and Methods: This observational, prospective-retrospective, single centre, continuous study was conducted in a tertiary care teaching hospital among paediatric patients of transfusion dependent β Thalassemia Major. Patients treated with deferasirox for not more than 12 weeks were enrolled. Details of blood transfusions, relevant investigations performed every 3 weeks and 3 months and drugs used were recorded in a pretested case record form. Parents were provided with a diary to record the details of ADRs. Data were analyzed for demographic characteristics, number and mean volume of blood transfusions, changes in serum ferritin and iron levels, number and types of ADRs and progression, causality, severity and preventability of ADRs. Results: Of the 60 patients enrolled, one patient was lost to follow up and four withdrew their consent. Of the remaining 55 patients, 36 were boys and 19 were girls (mean age: 6 ± 3.14 years), including patients of 1-3 years (11), 4-6 years (24), 7-10 years (12) and 11-12 years (8). Thirty six patients were born of consanguineous marriages. Adherence to blood transfusion guidelines and deferasirox prescribing and administration guidelines was observed. A serial and significant decrease in mean serum ferritin and serum iron at 3 weeks and 3 months with deferasirox treatment was observed in all age groups except that of 11-12 years. A total of 117 ADRs were observed in 52 patients from 19498 doses, most common being diarrhea (24), raised serum creatinine (15), raised hepatic enzymes (14), abdominal pain (14) and rashes (14). A reduction in dose was required in 32 cases, while a temporary stoppage was indicated in 41 cases. Deferasirox was the possible and probable cause of 65 and 51 ADRs respectively as assessed by WHO-UMC scale. Majority of ADRs were definitely preventable and mild in nature. Conclusion: β Thalassemia Major is more common in males. A rational prescribing of deferasirox was observed. Deferasirox effectively reduced serum ferritin and serum iron levels in these patients.



Publication History

Article published online:
06 July 2021

© 2017. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/.)

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  • References

  • 1 Benz EJ. Hemoglobinopathies. In: Longo D, Kasper D, Jameson J, Fauci A, Hauser S, Loscalzo J, editors. Harrison's Principles of Internal Medicine. 18th ed. New York: McGraw-Hill; 2012. p. 698-702.
  • 2 Galanello R, Piga A, Forni GL, Bertrand Y, Foschini ML, Bordone E, et al. Phase II clinical evaluation of deferasirox, a once-daily oral chelating agent, in pediatric patients with beta-thalassemia major. Haematologica 2006;91:1343-51.
  • 3 Maheshwari M, Arora S, Kabra M, Menon PS. Carrier screening and prenatal diagnosis of beta-thalassemia. Indian Pediatr 1999;36:1119-25.
  • 4 Indian Academy of Pediatrics. Guidelines for Diagnosis and Management of Thalassemia. IAP National Consensus Meeting on Thalassemia Held under IAP Action Plan; June, 2006. p. 169-202.
  • 5 Hoffbrand AV, Taher A, Cappellini MD. How I treat transfusional iron overload. Blood 2012;120:3657-69.
  • 6 Borgna-Pignatti C, Rugolotto S, De Stefano P, Piga A, Di Gregorio F, Gamberini MR, et al. Survival and disease complications in thalassemia major. Ann N Y Acad Sci 1998;850:227-31.
  • 7 Galanello R, Origa R. Beta-thalassemia. Orphanet J Rare Dis 2010;5:11.
  • 8 Gorakshakar AC, Colah RB. Cascade screening for beta-thalassemia: A practical approach for identifying and counseling carriers in India. Indian J Community Med 2009;34:354-6.
  • 9 Varawalla NY, Old JM, Sarkar R, Venkatesan R, Weatherall DJ. The spectrum of beta-thalassaemia mutations on the Indian subcontinent: The basis for prenatal diagnosis. Br J Haematol 1991;78:242-7.
  • 10 Olivieri NF, Brittenham GM. Iron-chelating therapy and the treatment of thalassemia. Blood 1997;89:739-61.
  • 11 Zurlo MG, De Stefano P, Borgna-Pignatti C, Di Palma A, Piga A, Melevendi C, et al. Survival and causes of death in thalassaemia major. Lancet 1989;2:27-30.
  • 12 Brittenham GM. Iron-chelating therapy for transfusional iron overload. N Engl J Med 2011;364:146-56.
  • 13 Cappellini MD, Cohen A, Piga A, Bejaoui M, Perrotta S, Agaoglu L, et al. Aphase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia. Blood 2006;107:3455-62.
  • 14 Chhotray GP, Dash BP, Ranjit M. Spectrum of hemoglobinopathies in Orissa, India. Hemoglobin 2004;28:117-22.
  • 15 Ahmad L, Hassan M, Rana SM, Mahboob S, Jabeen F. Prevalence of β-thalassemic patients associated with consanguinity and anti-HCV antibody positivity – A cross sectional study. Pak J Zool 2011;43:29-36.
  • 16 Talsania S, Talsania N, Nayak H. A cross sectional study of thalassemia in Ahmedabad city, Gujarat. (Hospital based). Healthline 2011;2:48-51.
  • 17 Nigam N, Musnhi N, Patel M, Soni A. Distribution of β thalassemia and its correlation with α thalassemia in Gujarati families. Int J Hum Genet 2003;3:221-4.
  • 18 Shah N, Mishra A, Chauhan D, Vora C, Shah NR. Study on effectiveness of transfusion program in thalassemia major patients receiving multiple blood transfusions at a transfusion centre in Western India. Asian J Transfus Sci 2010;4:94-8.
  • 19 Tanner MA, Galanello R, Dessi C, Smith GC, Westwood MA, Agus A, et al. Arandomized, 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 2007;115:1876-84.
  • 20 Wood JC. Cardiac iron across different transfusion-dependent diseases. Blood Rev 2008;22 Suppl 2:S14-21.
  • 21 Pennell DJ, Porter JB, Cappellini MD, El-Beshlawy A, Chan LL, Aydinok Y, et al. Efficacy of deferasirox in reducing and preventing cardiac iron overload in beta-thalassemia. Blood 2010;115:2364-71.
  • 22 Pennell DJ, Porter JB, Cappellini MD, Chan LL, El-Beshlawy A, Aydinok Y, et al. Continued improvement in myocardial T2* over two years of deferasirox therapy in ß-thalassemia major patients with cardiac iron overload. Haematologica 2011;96:48-54.
  • 23 Taher A, El-Beshlawy A, Elalfy MS, Al Zir K, Daar S, Habr D, et al. Efficacy and safety of deferasirox, an oral iron chelator, in heavily iron-overloaded patients with beta-thalassaemia: The ESCALATOR study. Eur J Haematol 2009;82:458-65.
  • 24 Piga A, Galanello R, Forni GL, Cappellini MD, Origa R, Zappu A, et al. Randomized phase II trial of deferasirox (Exjade, ICL670), a once-daily, orally-administered iron chelator, in comparison to deferoxamine in thalassemia patients with transfusional iron overload. Haematologica 2006;91:873-80.
  • 25 Wood JC, Kang BP, Thompson A, Giardina P, Harmatz P, Glynos T, et al. The effect of deferasirox on cardiac iron in thalassemia major: Impact of total body iron stores. Blood 2010;116:537-43.
  • 26 Aslam N, Mettu P, Marsano-Obando LS, Martin A. Deferasirox induced liver injury in haemochromatosis. J Coll Physicians Surg Pak 2010;20:551-3.