Abstract |
Allogeneic stem cell transplant is curative for haemophagocytic lymphohistiocytosis (HLH) and refractory Langerhans cell histiocytosis (LCH). However, patients frequently have significant pre-transplant morbidity and there is high TRM. Because HLH is caused by immune dysregulation, we surmised that a reduced-intensity conditioned (RIC) regimen might be sufficient for cure, while decreasing the TRM. In 2006, we reported the outcome of 12 patients treated with RIC SCT from a matched family/unrelated or haploidentical donor. Here we discuss the update of these patients, including a total of 25 patients treated with RIC SCT for HLH and three for LCH. Twenty-one of the twenty-five patients with HLH (84%) are alive and well with remission at a median of 36 months from SCT. Mortality included pneumonitis (n=3) and hepatic rupture (n=1). All three patients treated with RIC SCT for LCH remain alive and in remission at a median of 5.1 years from SCT. Seven of twenty-four survivors (one with LCH) have mixed chimerism but remain disease-free. These data are supported by other groups including 100% survival in seven patients with HLH and 78% survival of nine patients with LCH. In summary, RIC compares favourably with conventional SCT with long-term disease control in surviving patients with both HLH and LCL, despite a significant incidence of mixed chimerism.
|
Authors | N Cooper, K Rao, N Goulden, D Webb, P Amrolia, P Veys |
Journal | Bone marrow transplantation
(Bone Marrow Transplant)
Vol. 42 Suppl 2
Pg. S47-50
(Oct 2008)
ISSN: 1476-5365 [Electronic] England |
PMID | 18978744
(Publication Type: Journal Article, Review)
|
Topics |
- Disease-Free Survival
- Histiocytosis, Langerhans-Cell
(mortality, therapy)
- Humans
- Liver Diseases
(etiology, mortality)
- Living Donors
- Lymphohistiocytosis, Hemophagocytic
(mortality, therapy)
- Pneumonia
(etiology, mortality)
- Remission Induction
- Rupture, Spontaneous
- Stem Cell Transplantation
- Survival Rate
- Transplantation Chimera
- Transplantation, Homologous
|