Literature DB >> 23160007

Treosulfan-thiotepa-fludarabine-based conditioning regimen for allogeneic transplantation in patients with thalassemia major: a single-center experience from north India.

Dharma Choudhary1, Sanjeev Kumar Sharma, Nitin Gupta, Gaurav Kharya, Punita Pavecha, Anil Handoo, Rasika Setia, Satyendra Katewa.   

Abstract

Hematopoietic stem cell transplantation (HSCT) is the definite treatment for patients with thalassemia major. A busulfan (Bu) and cyclophosphamide (Cy)-based regimen has been the standard myeloablative chemotherapy, but it is associated with higher treatment-related toxicity, particularly in patients classified as high risk by the Pesaro criteria. Treosulfan-based conditioning regimens have been found to be equally effective and less toxic. Consequently, we analyzed the safety and efficacy of treosulfan/thiotepa/fludarabine (treo/thio/flu)-based conditioning regimens for allogeneic HSCT in patients with thalassemia major between February 2010 and September 2012. We compared those results retrospectively with results in patients who underwent previous HSCT with a Bu/Cy/antithymocyte globulin (ATG)-based conditioning regimen. A treo/thio/flu-based conditioning regimen was used in 28 consecutive patients with thalassemia major. The median patient age was 9.7 years (range, 2-18 years), and the mean CD34(+) stem cell dose was 6.18 × 10(6)/kg. Neutrophil and platelet engraftment occurred at a median of 15 days (range, 12-23 days) and 21 days (range, 14-34 days), respectively. Three patients developed veno-occlusive disease, 4 patients developed acute graft-versus-host disease (GVHD), and 2 patients had chronic GVHD. Treatment-related mortality (TRM) was 21.4%. Two patients experienced secondary graft rejection. We compared these results with results in patients who underwent previous HSCT using a Bu/Cy/ATG-based conditioning regimen. Twelve patients were treated with this protocol, at a median age of 7.2 years (range, 2-11 years). One patient had moderate veno-occlusive disease, 2 patients developed acute GVHD, 2 patients had chronic GVHD, and 2 patients experienced graft rejection. There was no TRM in this group. We found no significant differences between the 2 groups (treo/thio/flu vs Bu/Cy/ATG) in terms of the incidence of acute GVHD, chronic GVHD, TRM, and graft failure, although a trend toward higher TRM was seen with the treo/thio/flu regimen.
Copyright © 2013 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 23160007     DOI: 10.1016/j.bbmt.2012.11.007

Source DB:  PubMed          Journal:  Biol Blood Marrow Transplant        ISSN: 1083-8791            Impact factor:   5.742


  13 in total

Review 1.  Cure for thalassemia major - from allogeneic hematopoietic stem cell transplantation to gene therapy.

Authors:  Alok Srivastava; Ramachandran V Shaji
Journal:  Haematologica       Date:  2016-12-01       Impact factor: 9.941

2.  Hemopoietic stem cell transplantation in thalassemia: a report from the European Society for Blood and Bone Marrow Transplantation Hemoglobinopathy Registry, 2000-2010.

Authors:  D Baronciani; E Angelucci; U Potschger; J Gaziev; A Yesilipek; M Zecca; M G Orofino; C Giardini; A Al-Ahmari; S Marktel; J de la Fuente; A Ghavamzadeh; A A Hussein; C Targhetta; F Pilo; F Locatelli; G Dini; P Bader; C Peters
Journal:  Bone Marrow Transplant       Date:  2016-01-11       Impact factor: 5.483

Review 3.  Conditioning regimens in allo-SCT for thalassemia major.

Authors:  V Mathews; B N Savani
Journal:  Bone Marrow Transplant       Date:  2014-01-20       Impact factor: 5.483

4.  ATG vs thiotepa with busulfan and cyclophosphamide in matched-related bone marrow transplantation for thalassemia.

Authors:  Lawrence Faulkner; Cornelio Uderzo; Sadaf Khalid; Priya Marwah; Rajpreet Soni; Naila Yaqub; Samina Amanat; Itrat Fatima; Sarah Khan Gilani; Tatheer Zahra; Stalin Ramprakash; Lallindra Gooneratne; Ruwangi Dissanayake; Senani Williams; Wasantha Rathnayake; Reshma Srinivas; Amit Sedai; Ankita Kumari; Lailith Parmar; Rakesh Dhanya; Rajat Kumar Agarwal
Journal:  Blood Adv       Date:  2017-05-11

5.  Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel.

Authors:  Emanuele Angelucci; Susanne Matthes-Martin; Donatella Baronciani; Françoise Bernaudin; Sonia Bonanomi; Maria Domenica Cappellini; Jean-Hugues Dalle; Paolo Di Bartolomeo; Cristina Díaz de Heredia; Roswitha Dickerhoff; Claudio Giardini; Eliane Gluckman; Ayad Achmed Hussein; Naynesh Kamani; Milen Minkov; Franco Locatelli; Vanderson Rocha; Petr Sedlacek; Frans Smiers; Isabelle Thuret; Isaac Yaniv; Marina Cavazzana; Christina Peters
Journal:  Haematologica       Date:  2014-05       Impact factor: 9.941

6.  Busulfan-fludarabine- or treosulfan-fludarabine-based myeloablative conditioning for children with thalassemia major.

Authors:  Roswitha Lüftinger; Natalia Zubarovskaya; Christina Peters; Arjan Lankester; Selim Corbacioglu; Jacques-Emmanuel Galimard; Annamaria Cseh; Elisabeth Salzer; Franco Locatelli; Mattia Algeri; Akif Yesilipek; Josu de la Fuente; Antonella Isgrò; Amal Alseraihy; Emanuele Angelucci; Frans J Smiers; Giorgia La La Nasa; Marco Zecca; Tunc Fisgin; Emel Unal; Katharina Kleinschmidt
Journal:  Ann Hematol       Date:  2022-01-09       Impact factor: 3.673

7.  Treosulfan-based conditioning regimens for allogeneic haematopoietic stem cell transplantation in children with non-malignant diseases.

Authors:  M A Slatter; H Boztug; U Pötschger; K-W Sykora; A Lankester; I Yaniv; P Sedlacek; E Glogova; P Veys; A R Gennery; C Peters
Journal:  Bone Marrow Transplant       Date:  2015-08-10       Impact factor: 5.483

Review 8.  Unrelated donor stem cell transplantation for transfusion-dependent thalassemia.

Authors:  Shalini Shenoy; Alexis A Thompson
Journal:  Ann N Y Acad Sci       Date:  2016-03-21       Impact factor: 5.691

9.  Treosulfan-based conditioning and hematopoietic cell transplantation for nonmalignant diseases: a prospective multicenter trial.

Authors:  Lauri M Burroughs; Eneida R Nemecek; Troy R Torgerson; Barry E Storer; Julie-An Talano; Jennifer Domm; Roger H Giller; Akiko Shimamura; Colleen Delaney; Suzanne Skoda-Smith; Monica S Thakar; K Scott Baker; David J Rawlings; Janet A Englund; Mary E D Flowers; H Joachim Deeg; Rainer Storb; Ann E Woolfrey
Journal:  Biol Blood Marrow Transplant       Date:  2014-09-06       Impact factor: 5.742

10.  Pretransplant immunosuppression followed by reduced-toxicity conditioning and stem cell transplantation in high-risk thalassemia: a safe approach to disease control.

Authors:  Usanarat Anurathapan; Samart Pakakasama; Piya Rujkijyanont; Nongnuch Sirachainan; Duantida Songdej; Ampaiwan Chuansumrit; Somtawin Sirireung; Pimlak Charoenkwan; Arunee Jetsrisuparb; Surapol Issaragrisil; Artit Ungkanont; Rosarin Sruamsiri; Supanart Srisala; Borje S Andersson; Suradej Hongeng
Journal:  Biol Blood Marrow Transplant       Date:  2013-05-03       Impact factor: 5.742

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