Allele-level HLA matching for umbilical cord blood transplantation for non-malignant diseases in children: a retrospective analysis.

dc.contributor.author

Eapen, Mary

dc.contributor.author

Wang, Tao

dc.contributor.author

Veys, Paul A

dc.contributor.author

Boelens, Jaap J

dc.contributor.author

St Martin, Andrew

dc.contributor.author

Spellman, Stephen

dc.contributor.author

Bonfim, Carmem Sales

dc.contributor.author

Brady, Colleen

dc.contributor.author

Cant, Andrew J

dc.contributor.author

Dalle, Jean-Hugues

dc.contributor.author

Davies, Stella M

dc.contributor.author

Freeman, John

dc.contributor.author

Hsu, Katherine C

dc.contributor.author

Fleischhauer, Katharina

dc.contributor.author

Kenzey, Chantal

dc.contributor.author

Kurtzberg, Joanne

dc.contributor.author

Michel, Gerard

dc.contributor.author

Orchard, Paul J

dc.contributor.author

Paviglianiti, Annalisa

dc.contributor.author

Rocha, Vanderson

dc.contributor.author

Veneris, Michael R

dc.contributor.author

Volt, Fernanda

dc.contributor.author

Wynn, Robert

dc.contributor.author

Lee, Stephanie J

dc.contributor.author

Horowitz, Mary M

dc.contributor.author

Gluckman, Eliane

dc.contributor.author

Ruggeri, Annalisa

dc.date.accessioned

2022-03-23T18:52:50Z

dc.date.available

2022-03-23T18:52:50Z

dc.date.issued

2017-07

dc.date.updated

2022-03-23T18:52:50Z

dc.description.abstract

Background

The standard for selecting unrelated umbilical cord blood units for transplantation for non-malignant diseases relies on antigen-level (lower resolution) HLA typing for HLA-A and HLA-B, and allele-level for HLA-DRB1. We aimed to study the effects of allele-level matching at a higher resolution-HLA-A, HLA-B, HLA-C, and HLA-DRB1, which is the standard used for adult unrelated volunteer donor transplantation for non-malignant diseases-for umbilical cord blood transplantation.

Methods

We retrospectively studied 1199 paediatric donor-recipient pairs with allele-level HLA matching who received a single unit umbilical cord blood transplantation for non-malignant diseases reported to the Center for International Blood and Marrow Transplant Research or Eurocord and European Group for Blood and Marrow Transplant. Transplantations occurred between Jan 1, 2000, and Dec 31, 2012. The primary outcome was overall survival. The effect of HLA matching on survival was studied using a Cox regression model.

Findings

Compared with HLA-matched transplantations, mortality was higher with transplantations mismatched at two (hazard ratio [HR] 1·55, 95% CI 1·08-2·21, p=0·018), three (2·04, 1·44-2·89, p=0·0001), and four or more alleles (3·15, 2·16-4·58, p<0·0001). There were no significant differences in mortality between transplantations that were matched and mismatched at one allele (HR 1·18, 95% CI 0·80-1·72, p=0·39). Other factors associated with higher mortality included recipient cytomegalovirus seropositivity (HR 1·40, 95% CI 1·13-1·74, p=0·0020), reduced intensity compared with myeloablative conditioning regimens (HR 1·36, 1·10-1·68, p=0·0041), transplantation of units with total nucleated cell dose of more than 21 × 107 cells per kg compared with 21 × 107 cells per kg or less (HR 1·47, 1·11-1·95, p=0·0076), and transplantations done in 2000-05 compared with those done in 2006-12 (HR 1·64, 1·31-2·04, p<0·0001). The 5-year overall survival adjusted for recipient cytomegalovirus serostatus, conditioning regimen intensity, total nucleated cell dose, and transplantation period was 79% (95% CI 74-85) after HLA matched, 76% (71-81) after one allele mismatched, 70% (65-75) after two alleles mismatched, 62% (57-68) after three alleles mismatched, and 49% (41-57) after four or more alleles mismatched transplantations. Graft failure was the predominant cause of mortality.

Interpretation

These data support a change from current practice in that selection of unrelated umbilical cord blood units for transplantation for non-malignant diseases should consider allele-level HLA matching at HLA-A, HLA-B, HLA-C, and HLA-DRB1.

Funding

National Cancer Institute; National Heart, Lung, and Blood Institute; National Institute for Allergy and Infectious Diseases; US Department of Health and Human Services-Health Resources and Services Administration; and US Department of Navy.
dc.identifier

S2352-3026(17)30104-7

dc.identifier.issn

2352-3026

dc.identifier.issn

2352-3026

dc.identifier.uri

https://hdl.handle.net/10161/24620

dc.language

eng

dc.publisher

Elsevier BV

dc.relation.ispartof

The Lancet. Haematology

dc.relation.isversionof

10.1016/s2352-3026(17)30104-7

dc.subject

Fetal Blood

dc.subject

Humans

dc.subject

Histocompatibility Testing

dc.subject

Treatment Outcome

dc.subject

Survival Analysis

dc.subject

Retrospective Studies

dc.subject

Alleles

dc.subject

Adolescent

dc.subject

Child

dc.subject

Child, Preschool

dc.subject

Infant

dc.subject

Female

dc.subject

Male

dc.title

Allele-level HLA matching for umbilical cord blood transplantation for non-malignant diseases in children: a retrospective analysis.

dc.type

Journal article

duke.contributor.orcid

Kurtzberg, Joanne|0000-0002-3370-0703

pubs.begin-page

e325

pubs.end-page

e333

pubs.issue

7

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

pubs.organisational-group

Clinical Science Departments

pubs.organisational-group

Institutes and Centers

pubs.organisational-group

Pathology

pubs.organisational-group

Pediatrics

pubs.organisational-group

Duke Cancer Institute

pubs.organisational-group

Institutes and Provost's Academic Units

pubs.organisational-group

Initiatives

pubs.organisational-group

Duke Innovation & Entrepreneurship

pubs.organisational-group

Pediatrics, Transplant and Cellular Therapy

pubs.publication-status

Published

pubs.volume

4

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
p329 Eapen.pdf
Size:
234.57 KB
Format:
Adobe Portable Document Format
Description:
Published version