| Literature DB >> 29296723 |
Lawrence Faulkner1,2, Cornelio Uderzo1, Sadaf Khalid1, Priya Marwah3, Rajpreet Soni3, Naila Yaqub4, Samina Amanat4, Itrat Fatima4, Sarah Khan Gilani4, Tatheer Zahra4, Stalin Ramprakash2, Lallindra Gooneratne5, Ruwangi Dissanayake5, Senani Williams6, Wasantha Rathnayake6, Reshma Srinivas7, Amit Sedai7, Ankita Kumari7, Lailith Parmar7, Rakesh Dhanya7, Rajat Kumar Agarwal7.
Abstract
Matched-related bone marrow transplantation (BMT) may cure >80% of low-risk children with severe thalassemia (ST). Very long-term follow-up studies have shown how the standard busulfan-cyclophosphamide (BuCy) regimen may be associated with normalization of health-related quality of life, no second malignancies in the absence of chronic graft-versus-host disease, and fertility preservation in many patients. However, because BuCy may be associated with high rejection rates, some centers incorporate thiotepa (Tt) in busulfan- or treosulfan-based regimens, a combination that may increase the risk of permanent infertility. This study retrospectively compares matched-related BMT outcomes in 2 groups of low-risk ST patients conditioned with either Tt or anti-thymocyte globulin (ATG) in addition to BuCy. A total of 81 consecutive first BMTs were performed in 5 collaborating startup BMT centers in the Indian subcontinent between January 2009 and January 2016; 30 patients were transplanted after conditioning with Tt-BuCy between January 2009 and July 2013, whereas between August 2013 and January 2016, 51 patients received ATG-BuCy. All patients were <15 years and had no hepatomegaly (liver ≤2 cm from costal margin). Actuarial overall survival in the Tt-BuCy and ATG-BuCy groups was 87% and 94% and thalassemia-free survival was 80% and 85% at a median follow-up of 37 and 17 months, respectively, with no significant differences by log-rank statistics. Substituting Tt with ATG in the standard BuCy context seems safe and effective and may decrease transplant-related mortality. Higher fertility rates are expected for patients who received ATG-BuCy.Entities:
Year: 2017 PMID: 29296723 PMCID: PMC5727808 DOI: 10.1182/bloodadvances.2016004119
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529