The role of HLA matching in unrelated donor hematopoietic stem cell transplantation for sickle cell disease in Europe.
Eliane GluckmanJosu de la FuenteBarbara CappelliGraziana M ScigliuoloFernanda VoltKarina Tozatto-MaioVanderson RochaMina TommasoFarah O'BoyleFrans SmiersClaudia Bettoni Da Cunha-RiehmElisabetta CaloreSonia BonanomiStelios GraphakosAnna PaisiouMichael H AlbertAnnalisa RuggeriMarco ZeccaArjan C LankesterSelim Corbacioglunull nullPublished in: Bone marrow transplantation (2020)
We report the results of an analysis of unrelated allogeneic hematopoietic stem cell transplantations (HSCT) in 71 patients with sickle cell disease (SCD) transplanted in EBMT centers between 2005 and 2017. Median age was 9.3 years; graft type was bone marrow in 79% and peripheral blood in 21%. Recipient-donor HLA match at high resolution typing was 10/10 in 31, 9/10 in 20, and 8/10 in 4 patients; the other patients had intermediate resolution typing. The most frequent conditioning regimens were fludarabine-thiotepa-treosulfan (64%) or busulfan-cyclophosphamide (12%). Cumulative incidence of neutrophil engraftment was 92%; platelet engraftment was 90%. Eleven patients (15%) experienced graft failure. Grade II-IV acute graft-vs.-host disease (GvHD) was 23%; 3-year chronic GvHD was 23%. Three-year overall survival (OS) was 88 ± 4%. GRFS was 62 ± 6%. HLA matching was the most significant risk factor for OS: 3-year OS was 96 ± 4% in 10/10 group vs. 75 ± 10% in 9-8/10 (p = 0.042); GRFS was 69 ± 9% vs. 50 ± 12% (p = 0.114), respectively. In conclusion, unrelated donor HSCT is a valid option for SCD patients who lack an HLA-identical sibling donor, preferably in the context of clinical trials. Using a 10/10 HLA-matched unrelated donor yields better survival indicating that HLA matching is an important donor selection factor in this nonmalignant disease.
Keyphrases
- end stage renal disease
- bone marrow
- chronic kidney disease
- ejection fraction
- newly diagnosed
- clinical trial
- high resolution
- sickle cell disease
- mesenchymal stem cells
- randomized controlled trial
- low dose
- intensive care unit
- risk factors
- stem cell transplantation
- acute respiratory distress syndrome
- single molecule
- high dose
- high speed
- free survival
- genetic diversity