Fludarabine‐based reduced‐intensity conditioning regimen for hematopoietic stem cell transplantation in primary hemophagocytic lymphohistiocytosis. (10th January 2014)

• Record Type: Journal Article
• Authors: Hamidieh, Amir Ali; Pourpak, Zahra; Hashemi, Susan; Yari, Kolsoum; Fazlollahi, Mohammad Reza; Movahedi, Masoud; Behfar, Maryam; Moin, Mostafa; Ghavamzadeh, Ardeshir
• Is Part Of: European journal of haematology. Volume 92:Number 4(2014:Apr.)
• Page Start: 331
• Page End: 336
• Publication Date: 2014-01-10
• Subjects: Hematology -- Periodicals; Blood -- Diseases -- Periodicals; Blood -- Periodicals; 616.15005
• DOI: 10.1111/ejh.12244
• Languages: English
• ISSNs: 0902-4441

Abstract

<abstract abstract-type="main" id="ejh12244-abs-0001"> <title>Abstract</title> <sec id="ejh12244-sec-0001" sec-type="section"> <title>Objective</title> <p>Primary hemophagocytic lymphohistiocytosis (HLH) is a life‐threatening condition that clinically characterized by fever, hepatosplenomegaly, and cytopenia. Hematopoietic stem cell transplantation (HSCT) is the only curative treatment option for patients diagnosed with primary HLH.</p> </sec> <sec id="ejh12244-sec-0002" sec-type="section"> <title>Methods</title> <p>In this prospective study, we analyzed the outcome of 10 pediatric patients with primary HLH who had received HSCT, using reduced‐intensity conditioning (RIC) regimen from 2007 to 2012. The median age at transplantation was 22.6 months (range: 6–60). All of the patients received the same RIC regimen based on the use of fludarabine in combination with melphalan and horse antithymocyte globulin (ATG). Cyclosporine and methylprednisolone were used as graft‐vs.‐host disease (GvHD) prophylaxis.</p> </sec> <sec id="ejh12244-sec-0003" sec-type="section"> <title>Results</title> <p>Hematopoietic engraftment occurred in all patients. At the present time, 8 patients with a median follow‐up of 39 months are still alive and all of them are disease free. Acute and chronic GvHD developed in 6 and 2 patients, retrospectively. Two patients died of sepsis and chronic GvHD during the study.</p> </sec> <sec id="ejh12244-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Because of pretransplant infections caused by underlying immunodeficiency in patients with primary HLH, the use of less toxic regimen with RIC seems to be highly effective in this regard. Recipients of RIC transplant, with either full or mixed chimerism, had a long‐term survival rate with no manifestation of primary HLH symptoms.</p> </sec> </abstract>