| Literature DB >> 25064743 |
Usanarat Anurathapan1, Samart Pakakasama1, Pimsiri Mekjaruskul1, Nongnuch Sirachainan1, Duantida Songdej1, Ampaiwan Chuansumrit1, Pimlak Charoenkwan2, Arunee Jetsrisuparb3, Kleebsabai Sanpakit4, Bunchoo Pongtanakul4, Piya Rujkijyanont5, Arunotai Meekaewkunchorn6, Rosarin Sruamsiri7, Artit Ungkanont8, Surapol Issaragrisil9, Borje S Andersson10, Suradej Hongeng11.
Abstract
Improving outcomes among class 3 thalassemia patients receiving allogeneic hematopoietic stem cell transplantations (HSCT) remains a challenge. Before HSCT, patients who were ≥ 7 years old and had a liver size ≥ 5 cm constitute what the Center for International Blood and Marrow Transplant Research defined as a very high-risk subset of a conventional high-risk class 3 group (here referred to as class 3 HR). We performed HSCT in 98 patients with related and unrelated donor stem cells. Seventy-six of the patients with age < 10 years received the more conventional myeloablative conditioning (MAC) regimen (cyclophosphamide, busulfan, ± fludarabine); the remaining 22 patients with age ≥ 10 years and hepatomegaly (class 3 HR), and in several instances additional comorbidity problems, underwent HSCT with a novel reduced-toxicity conditioning (RTC) regimen (fludarabine and busulfan). We then compared the outcomes between these 2 groups (MAC versus RTC). Event-free survival (86% versus 90%) and overall survival (95% versus 90%) were not significantly different between the respective groups; however, there was a higher incidence of serious treatment-related complications in the MAC group, and although we experienced 6 graft failures in the MAC group (8%), there were none in the RTC group. Based on these results, we suggest that (1) class 3 HR thalassemia patients can safely receive HSCT with our novel RTC regimen and achieve the same excellent outcome as low/standard-risk thalassemia patients who received the standard MAC regimen, and further, (2) that this novel RTC approach should be tested in the low/standard-risk patient population.Entities:
Keywords: Myeloablative; Reduced toxicity; Thalassemia
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Year: 2014 PMID: 25064743 PMCID: PMC5538782 DOI: 10.1016/j.bbmt.2014.07.016
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742