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Allogeneic hematopoietic stem cell transplantation in leukocyte adhesion deficiency type I and III.


ABSTRACT: Type I and III leukocyte adhesion deficiencies (LADs) are primary immunodeficiency disorders resulting in early death due to infections and additional bleeding tendency in LAD-III. The curative treatment of LAD-I and LAD-III is allogeneic hematopoietic stem cell transplantation (allo-HSCT). In this retrospective multicenter study, data were collected using the European Society for Blood and Marrow Transplantation registry; we analyzed data from 84 LAD patients from 33 centers, all receiving an allo-HSCT from 2007 to 2017. The 3-year overall survival estimate (95% confidence interval [CI]) was 83% (74-92) for the entire cohort: 84% (75-94) and 75% (50-100) for LAD-I and LAD-III, respectively. We observed cumulative incidences (95% CI) of graft failure (GF) at 3 years of 17% (9%-26%) and grade II to IV acute graft-versus-host disease (aGVHD) at 100 days of 24% (15%-34%). The estimate (95% CI) at 3 years for GF- and GVHD-II to IV-free survival as event-free survival (EFS) was 56% (46-69) for the entire cohort; 58% (46-72) and 56% (23-88) for LAD-I and LAD-III, respectively. Grade II to IV acute GVHD was a relevant risk factor for death (hazard ratio 3.6; 95% CI 1.4-9.1; P = .006). Patients' age at transplant ?13 months, transplantation from a nonsibling donor, and any serological cytomegalovirus mismatch in donor-recipient pairs were significantly associated with severe acute GVHD and inferior EFS. The choice of busulfan- or treosulfan-based conditioning, type of GVHD prophylaxis, and serotherapy did not impact overall survival, EFS, or aGVHD. An intrinsic inflammatory component of LAD may contribute to inflammatory complications during allo-HSCT, thus providing the rationale for considering anti-inflammatory therapy pretreatment.

SUBMITTER: Bakhtiar S 

PROVIDER: S-EPMC7805328 | biostudies-literature | 2021 Jan

REPOSITORIES: biostudies-literature

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Allogeneic hematopoietic stem cell transplantation in leukocyte adhesion deficiency type I and III.

Bakhtiar Shahrzad S   Salzmann-Manrique Emilia E   Blok Henric-Jan HJ   Eikema Dirk-Jan DJ   Hazelaar Sheree S   Ayas Mouhab M   Toren Amos A   Goldstein Gal G   Moshous Despina D   Locatelli Franco F   Merli Pietro P   Michel Gerard G   Öztürk Gülyüz G   Schulz Ansgar A   Heilmann Carsten C   Ifversen Marianne M   Wynn Rob F RF   Aleinikova Olga O   Bertrand Yves Y   Tbakhi Abdelghani A   Veys Paul P   Karakukcu Musa M   Kupesiz Alphan A   Ghavamzadeh Ardeshir A   Handgretinger Rupert R   Unal Emel E   Perez-Martinez Antonio A   Gokce Muge M   Porta Fulvio F   Aksu Tekin T   Karasu Gülsün G   Badell Isabel I   Ljungman Per P   Skorobogatova Elena E   Yesilipek Akif A   Zuckerman Tsila T   Bredius Robbert R G RRG   Stepensky Polina P   Shadur Bella B   Slatter Mary M   Gennery Andrew R AR   Albert Michael H MH   Bader Peter P   Lankester Arjan A  

Blood advances 20210101 1


Type I and III leukocyte adhesion deficiencies (LADs) are primary immunodeficiency disorders resulting in early death due to infections and additional bleeding tendency in LAD-III. The curative treatment of LAD-I and LAD-III is allogeneic hematopoietic stem cell transplantation (allo-HSCT). In this retrospective multicenter study, data were collected using the European Society for Blood and Marrow Transplantation registry; we analyzed data from 84 LAD patients from 33 centers, all receiving an a  ...[more]

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