Literature DB >> 33481797

Outcome of iron reduction therapy in ex-thalassemics.

Fouzia N Aboobacker1, Gaurav Dixit1, Kavitha M Lakshmi1, Anu Korula1, Aby Abraham1, Biju George1, Vikram Mathews1, Alok Srivastava1.   

Abstract

There is limited data on iron reduction therapy (IRT) after successful allogeneic haematopoietic stem cell transplantation (aHSCT) for patients with thalassemia major (TM). We present the long term outcome of IRT in 149 patients with TM who underwent aHSCT during January, 2001-December, 2012. The median age was 7 years (range:1-18) and 92 (61.7%) belonged to Pesaro class 3 with a median ferritin at aHSCT of 2480ng/ml (range:866-8921). IRT was reinitiated post-aHSCT at a median of 14 months (range:5-53) post aHSCT with phlebotomy alone in 10 (6.7%) patients or iron chelation alone in 60 (40.3%) patients while 79 (53%) were treated with the combination. Reduction in serum ferritin/month [absolute quantity (ng/ml/month) was as follows: 87 (range:33-195), 130 (range:17-1012) and 147 (range:27.7-1427) in the phlebotomy, chelation and combination therapy groups, respectively (p = 0.038). With a median follow up of 80 months (range:37-182), target ferritin level of <300ng/ml was achieved in 59(40%) while a level <500ng/ml was achieved in 88 patients (59%) in a median duration of 41 months of IRT (range: 3-136). Patients in class III risk category and higher starting serum ferritin levels (>2500ng/ml) were associated with delayed responses to IRT. Our data shows that IRT may be needed for very long periods in ex-thalassaemics to achieve target ferritin levels and should therefore be carefully planned and initiated as soon as possible after aHSCT. A combination of phlebotomy and iron chelators is more effective in reducing iron overload.

Entities:  

Year:  2021        PMID: 33481797      PMCID: PMC7822270          DOI: 10.1371/journal.pone.0238793

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


  20 in total

1.  Ferritin trends do not predict changes in total body iron in patients with transfusional iron overload.

Authors:  Mammen Puliyel; Richard Sposto; Vasilios A Berdoukas; Thomas C Hofstra; Anne Nord; Susan Carson; John Wood; Thomas D Coates
Journal:  Am J Hematol       Date:  2014-02-28       Impact factor: 10.047

2.  Deferasirox use after hematopoietic stem cell transplantation in pediatric patients with beta-thalassemia major: preliminary results.

Authors:  Sule Unal; Baris Kuskonmaz; Tuncay Hazirolan; Gonca Eldem; Selin Aytac; Mualla Cetin; Duygu Uckan; Fatma Gumruk
Journal:  Pediatr Hematol Oncol       Date:  2010-09       Impact factor: 1.969

3.  Assessment of liver iron content in 271 patients: a reevaluation of direct and indirect methods.

Authors:  P Brissot; M Bourel; D Herry; J P Verger; M Messner; C Beaumont; F Regnouard; B Ferrand; M Simon
Journal:  Gastroenterology       Date:  1981-03       Impact factor: 22.682

4.  Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine.

Authors:  Caterina Borgna-Pignatti; Simone Rugolotto; Piero De Stefano; Huaqing Zhao; Maria Domenica Cappellini; Giovanni Carlo Del Vecchio; Maria Antonietta Romeo; Gian Luca Forni; Maria Rita Gamberini; Roberta Ghilardi; Antonio Piga; Avital Cnaan
Journal:  Haematologica       Date:  2004-10       Impact factor: 9.941

5.  Survival in medically treated patients with homozygous beta-thalassemia.

Authors:  N F Olivieri; D G Nathan; J H MacMillan; A S Wayne; P P Liu; A McGee; M Martin; G Koren; A R Cohen
Journal:  N Engl J Med       Date:  1994-09-01       Impact factor: 91.245

6.  Developing an algorithm of informative markers for evaluation of chimerism after allogeneic bone marrow transplantation.

Authors:  S Sellathamby; P Balasubramanian; S Sivalingam; R V Shaji; V Mathews; B George; A Viswabandya; A Srivastava; M Chandy
Journal:  Bone Marrow Transplant       Date:  2006-04       Impact factor: 5.483

7.  Hepatic iron stores and plasma ferritin concentration in patients with sickle cell anemia and thalassemia major.

Authors:  G M Brittenham; A R Cohen; C E McLaren; M B Martin; P M Griffith; A W Nienhuis; N S Young; C J Allen; D E Farrell; J W Harris
Journal:  Am J Hematol       Date:  1993-01       Impact factor: 10.047

8.  A Phase II, Multicenter, Single-Arm Study to Evaluate the Safety and Efficacy of Deferasirox after Hematopoietic Stem Cell Transplantation in Children with β-Thalassemia Major.

Authors:  Mehmet Akif Yesilipek; Gulsun Karasu; Zuhre Kaya; Baris B Kuskonmaz; Vedat Uygun; Ilkiz Dag; Onur Ozudogru; Mehmet Ertem
Journal:  Biol Blood Marrow Transplant       Date:  2017-11-16       Impact factor: 5.742

9.  A new stratification strategy that identifies a subset of class III patients with an adverse prognosis among children with beta thalassemia major undergoing a matched related allogeneic stem cell transplantation.

Authors:  Vikram Mathews; Biju George; Uday Deotare; Kavitha M Lakshmi; Auro Viswabandya; Dolly Daniel; Mammen Chandy; Alok Srivastava
Journal:  Biol Blood Marrow Transplant       Date:  2007-06-22       Impact factor: 5.742

10.  Marrow transplantation for patients with thalassemia: results in class 3 patients.

Authors:  G Lucarelli; R A Clift; M Galimberti; P Polchi; E Angelucci; D Baronciani; C Giardini; M Andreani; M Manna; S Nesci; F Agostinelli; S Rapa; M Ripalti; F Albertini
Journal:  Blood       Date:  1996-03-01       Impact factor: 22.113

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.