Literature DB >> 18574445

Second hematopoietic SCT in patients with thalassemia recurrence following rejection of the first graft.

J Gaziev1, P Sodani, G Lucarelli, P Polchi, S Marktel, K Paciaroni, M Marziali, A Isgrò, M D Simone, A Roveda, A Montuoro, A Lanti, C Alfieri, G De Angelis, C Gallucci, F Ciceri, M G Roncarolo.   

Abstract

There is a substantial incidence of graft failure in patients with thalassemia after myeloablative conditioning regimens especially in class 3 patients in whom its incidence could be as high as 8-38.5%. Most patients with graft failure have recurrence of thalassemic marrow. Historically, results of second transplants for thalassemia were poor because of a high rejection rate and/or increased TRM. Sixteen patients with thalassemia recurrence following rejection of the first graft and with a median age of 9 years (range, 4-20) were given second transplants using BM (n=7) or PBSC (n=9) after preparation with a new treatment protocol. All but two patients received stem cells from the same donor. The median interval between two transplants was 28 months (range, 8-204). The sustained engraftment rate was high (94%) with only one patient having primary graft failure. The probability of overall survival, event-free survival, TRM and graft failure were 79, 79, 16 and 6%, respectively. There were three transplant-related deaths. Thirteen patients are alive with Lansky/Karnofsky score of 100. This intensified treatment protocol was well tolerated with no significant increase in toxicity. The excellent results obtained with this new preparative regimen allow us to recommend it for second transplantation for patients with thalassemia recurrence.

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Year:  2008        PMID: 18574445     DOI: 10.1038/bmt.2008.175

Source DB:  PubMed          Journal:  Bone Marrow Transplant        ISSN: 0268-3369            Impact factor:   5.483


  6 in total

1.  Second bone marrow transplantation for patients with thalassemia: risks and benefits.

Authors:  Polina Stepensky; Reuven Or; Michael Y Shapira; Shoshana Revel-Vilk; Jerry Stein; Igor B Resnick
Journal:  Haematologica       Date:  2009-09       Impact factor: 9.941

2.  Second BMT for thalassemia major using CY post transplant.

Authors:  N Yaqub; S Khalid; F Itrat; A Khan; S K Gilani; M E Missiry; M H Hussain; C Uderzo; L Faulkner
Journal:  Bone Marrow Transplant       Date:  2014-03-10       Impact factor: 5.483

3.  Second allogeneic hematopoietic cell transplantation for graft failure: poor outcomes for neutropenic graft failure.

Authors:  Troy C Lund; Jessica Liegel; Nelli Bejanyan; Paul J Orchard; Qing Cao; Jakub Tolar; Claudio Brunstein; John E Wagner; Michael R Verneris; Daniel Weisdorf
Journal:  Am J Hematol       Date:  2015-10       Impact factor: 10.047

4.  HLA-matched sibling bone marrow transplantation for β-thalassemia major.

Authors:  Mitchell Sabloff; Mammen Chandy; Zhiwei Wang; Brent R Logan; Ardeshir Ghavamzadeh; Chi-Kong Li; Syed Mohammad Irfan; Christopher N Bredeson; Morton J Cowan; Robert Peter Gale; Gregory A Hale; John Horan; Suradej Hongeng; Mary Eapen; Mark C Walters
Journal:  Blood       Date:  2010-11-30       Impact factor: 22.113

5.  Hematopoietic stem cell transplantation in thalassemia and sickle cell disease. Unicenter experience in a multi-ethnic population.

Authors:  Marco Marziali; Antonella Isgrò; Javid Gaziev; Guido Lucarelli
Journal:  Mediterr J Hematol Infect Dis       Date:  2009-12-26       Impact factor: 2.576

Review 6.  Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area.

Authors:  Mohamad H Qari; Yasser Wali; Muneer H Albagshi; Mohammad Alshahrani; Azzah Alzahrani; Ibrahim A Alhijji; Abdulkareem Almomen; Abdullah Aljefri; Hussain H Al Saeed; Shaker Abdullah; Ahmad Al Rustumani; Khoutir Mahour; Shaker A Mousa
Journal:  Orphanet J Rare Dis       Date:  2013-09-17       Impact factor: 4.123

  6 in total

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