| Literature DB >> 25817915 |
Paul A Veys1, Vasanta Nanduri2, K Scott Baker3, Wensheng He4, Giuseppe Bandini5, Andrea Biondi6, Arnaud Dalissier7, Jeffrey H Davis8, Gretchen M Eames9, R Maarten Egeler10, Alexandra H Filipovich11, Alain Fischer12, Herbert Jürgens13, Robert Krance14, Edoardo Lanino15, Wing H Leung16, Susanne Matthes17, Gérard Michel18, Paul J Orchard19, Anna Pieczonka20, Olle Ringdén21,22, Paul G Schlegel23, Anne Sirvent24, Kim Vettenranta25, Mary Eapen4.
Abstract
Patients with Langerhans cell histiocytosis (LCH) refractory to conventional chemotherapy have a poor outcome. There are currently two promising treatment strategies for high-risk patients: the first involves the combination of 2-chlorodeoxyadenosine and cytarabine; the other approach is allogeneic haematopoietic stem cell transplantation (HSCT). Here we evaluated 87 patients with high-risk LCH who were transplanted between 1990 and 2013. Prior to the year 2000, most patients underwent HSCT following myeloablative conditioning (MAC): only 5 of 20 patients (25%) survived with a high rate (55%) of transplant-related mortality (TRM). After the year 2000 an increasing number of patients underwent HSCT with reduced intensity conditioning (RIC): 49/67 (73%) patients survived, however, the improved survival was not overtly achieved by the introduction of RIC regimens with similar 3-year probability of survival after MAC (77%) and RIC transplantation (71%). There was no significant difference in TRM by conditioning regimen intensity but relapse rates were higher after RIC compared to MAC regimens (28% vs. 8%, P = 0·02), although most patients relapsing after RIC transplantation could be salvaged with further chemotherapy. HSCT may be a curative approach in 3 out of 4 patients with high risk LCH refractory to chemotherapy: the optimal choice of HSCT conditioning remains uncertain.Entities:
Keywords: Langerhans cell histiocytosis; allogeneic transplantation; conditioning regimen intensity; survival; treatment failure
Mesh:
Year: 2015 PMID: 25817915 PMCID: PMC4433436 DOI: 10.1111/bjh.13347
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998