Hematopoietic stem cell transplantation for adolescents and adults with inborn errors of immunity: an EBMT IEWP study.
Michael H AlbertTiarlan SiraitDirk-Jan EikemaKaterina BakuninaClaudia WehrFelipe SuarezMaria Laura FoxNizar MahlaouiAndrew R GenneryArjan C LankesterRita BeierMaria Ester BernardoVenetia BigleyCaroline A LindemansSiobhan O BurnsBen CarpenterJaroslaw DybkoTayfun GüngörFabian H HauckSu Han LumDmitry BalashovRichard P MeiselDespina MoshousAnsgar SchulzCarsten SpeckmannMary A SlatterBrigitte StrahmDuygu Uckan-CetinkayaIsabelle MeytsTanja C ValléeRobert WynnBénédicte NevenEmma C MorrisAlessandro AiutiAlexei MaschanMahmoud AljurfTobias Gedde-DahlGunhan GurmanVictoria BordonGergely KrivánFranco LocatelliFulvio PortaDavid ValcárcelYves BeguinMaura FaraciNicolaus KrögerAleksandr KulaginPeter J ShawJoan Hendrik VeelkenCristina Diaz de HerediaFranca FagioliMatthias FelberBernd GruhnWolfgang HolterClaudia RössigPetr SedlacekJane ApperleyMouhab AyasIvana BodovaGoda ChoiJ J CornelissenAnne SirventAnjum KhanAlphan KupesizStig LenhoffHakan OzdoguNicolas von der WeidMontserrat RoviraRik SchotsDonald C VinhPublished in: Blood (2022)
Allogeneic hematopoietic stem cell transplantation (HSCT) is the gold standard curative therapy for infants and children with many inborn errors of immunity (IEI), but adolescents and adults with IEI are rarely referred for transplant. Lack of published HSCT outcome data outside small, single-center studies and perceived high risk of transplant-related mortality have delayed the adoption of HSCT for IEI patients presenting or developing significant organ damage later in life. This large retrospective, multicenter HSCT outcome study reports on 329 IEI patients (age range, 15-62.5 years at HSCT). Patients underwent first HSCT between 2000 and 2019. Primary endpoints were overall survival (OS) and event-free survival (EFS). We also evaluated the influence of IEI-subgroup and IEI-specific risk factors at HSCT, including infections, bronchiectasis, colitis, malignancy, inflammatory lung disease, splenectomy, hepatic dysfunction, and systemic immunosuppression. At a median follow-up of 44.3 months, the estimated OS at 1 and 5 years post-HSCT for all patients was 78% and 71%, and EFS was 65% and 62%, respectively, with low rates of severe acute (8%) or extensive chronic (7%) graft-versus-host disease. On univariate analysis, OS and EFS were inferior in patients with primary antibody deficiency, bronchiectasis, prior splenectomy, hepatic comorbidity, and higher hematopoietic cell transplant comorbidity index scores. On multivariable analysis, EFS was inferior in those with a higher number of IEI-associated complications. Neither age nor donor had a significant effect on OS or EFS. We have identified age-independent risk factors for adverse outcome, providing much needed evidence to identify which patients are most likely to benefit from HSCT.
Keyphrases
- end stage renal disease
- ejection fraction
- chronic kidney disease
- newly diagnosed
- risk factors
- prognostic factors
- young adults
- bone marrow
- stem cells
- systematic review
- type diabetes
- emergency department
- acute myeloid leukemia
- depressive symptoms
- cardiovascular disease
- free survival
- cystic fibrosis
- patient safety
- cross sectional
- acute lymphoblastic leukemia
- hematopoietic stem cell
- cardiovascular events
- smoking cessation
- patient reported
- ulcerative colitis
- cell therapy
- case control