For patients with inherited BM failure (BMF) or those with acquired BMF who fail immunosuppressive therapy and who lack a suitable alternative donor, the prognosis remains poor. Umbilical cord blood transplantation has extended the availability of hematopoietic stem cell transplantation in the absence of a suitable donor. A recent EBMT study confirmed the feasibility of this treatment and highlighted the fundamental role of the TNC dose (43.9 Â 10 7 /kg TNC/kg) on both engraftment and OS using cord blood as stem cell source in severe aplastic anemia. However, this procedure is still experimental and should be evaluated only through prospective clinical trials. (2013) 48, 201-202; doi:10.1038/bmt.2012.252; published online 7 January 2013
Bone Marrow TransplantationKeywords: cord blood; transplantation; aplastic anemia CORD BLOOD TRANSPLANTATION APLASTIC ANEMIA Acquired bone marrow failure (BMF) syndromes, such as severe aplastic anemia (SAA) or inherited Fanconi anemia, are rare diseases. The outcome of these patients has greatly improved over time, but is still poor for patients who lack a sibling donor and who failed or relapsed after immunosuppressive therapy (IST). Use of alternative donors has been historically associated with poor long-term survival. 1-3 However, recently, transplantation from unrelated donors has improved significantly because of better HLA matching, optimization of the conditioning regimen and improvement in supportive care. [4][5][6] For patients with inherited BMF or those with acquired BMF who fail IST and who lack a suitable alternative donor, the prognosis remains, however, extremely poor. Umbilical cord blood transplantation (UCBT) has extended the availability of hematopoietic SCT in the absence of a suitable donor. To date, double UCBT has been reported in only few patients with BMF.We evaluated this procedure in 14 patients (8 Fanconi anemia, 5 SAA and 1 paroxysmal nocturnal hemoglobinuria (PNH)) who received double cord blood transplantation (dUCBT) from 2004 to 2007 in Saint Louis Hospital in Paris, France. 7 With a median follow-up of 23 months, the estimated 2 year OS rates were 80±17% and 33±16% for patients with acquired and inherited BMF syndromes, respectively. Transplantation of two partially HLAmatched UCB thus enabled salvage treatment of high-risk patients with BMF syndromes. However, as dUCBT is associated with high incidence of GVHD, in spite of our limited experience, when possible, we have recommended the use of only one cord blood unit with high number of cells and not more than 1 out of 6 HLA mismatch in patients with Fanconi Anemia. 8 Results of single unit UCBT for patients with Fanconi anemia have been reported. OS was 40 ± 5% and factors associated with favorable outcome were use of fludarabine in the conditioning regimen, number of nucleated cells infused X4.9 Â 10 7 /kg, and negative CMV serology in the recipient. 2 Regarding results of UCBT in patients with acquired SAA, we have reported an analysis on 71 patients (33 males) diagnosed with SAA, (9 with PN...