001     277884
005     20240229162350.0
024 7 _ |a 10.3238/arztebl.m2023.0031
|2 doi
024 7 _ |a pmid:36949660
|2 pmid
024 7 _ |a pmc:PMC10366961
|2 pmc
037 _ _ |a DKFZ-2023-01552
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Fleischhauer, Katharina
|0 P:(DE-HGF)0
|b 0
245 _ _ |a Donor Selection for Allogeneic Hematopoietic Cell Transplantation.
260 _ _ |a Köln
|c 2023
|b Dt. Ärzte-Verl.
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1690875204_20937
|2 PUB:(DE-HGF)
|x Review Article
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a In Germany, each year over 3000 patients with malignant and non-malignant hematologic and systemic diseases are treated by allo - geneic hematopoietic cell transplantation (HCT). Genetic donor-recipient disparities, especially those concerning variable human leukocyte antigens (HLA), mediate both an immunotherapeutic effect and the risk of damage to healthy tissues ('graft-versus-host disease'). The adoption of evidencebased strategies for donor selection has been crucial for the continuous improvement of survival rates after allogeneic HCT, with over 50% of patients transplanted for standard indications-such as early-stage acute myeloid leukemia-alive at three years post-transplant.The PubMed database was selectively searched for literature on immunogenetic and clinical factors relevant to allogeneic HCT, as part of the process of establishing a German consensus statement on HCT donor selection.The most important factor in donor selection is a match for the five major HLA loci (HLA-A, -B, -C, -DR, -DQ), either in genetically HLAidentical siblings or in unrelated but fully HLA-compatible donors from international registries. Additional selection criteria for the latter include com - patibility for the HLA-DP locus, donor age and sex, cytomegalovirus serostatus, and blood group. Related donors identical for only 50% of the HLA genes (haploidentical donors) as well as unrelated donors with a single HLA mismatch are both valid alternatives although they are associated with an up to 10% higher risk of mortality.The refinement of donor selection strategies has been instrumental for the continuous improvement of patient survival rates after allogeneic HCT witnessed over the past decades. An interdisciplinary approach to donor selection based on up-to-date scientific evidence is crucial for optimizing patient outcomes.
536 _ _ |a 899 - ohne Topic (POF4-899)
|0 G:(DE-HGF)POF4-899
|c POF4-899
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: inrepo02.dkfz.de
650 _ 7 |a HLA Antigens
|2 NLM Chemicals
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Donor Selection
|2 MeSH
650 _ 2 |a Hematopoietic Stem Cell Transplantation
|2 MeSH
650 _ 2 |a Graft vs Host Disease: prevention & control
|2 MeSH
650 _ 2 |a Unrelated Donors
|2 MeSH
650 _ 2 |a Leukemia, Myeloid, Acute
|2 MeSH
650 _ 2 |a HLA Antigens
|2 MeSH
650 _ 2 |a Retrospective Studies
|2 MeSH
700 1 _ |a Tran, Thuong Hien
|b 1
700 1 _ |a Meisel, Roland
|b 2
700 1 _ |a Mytilineos, Joannis
|b 3
700 1 _ |a Dreger, Peter
|b 4
700 1 _ |a Kröger, Nicolaus
|b 5
773 _ _ |a 10.3238/arztebl.m2023.0031
|g Vol. 120, no. 15
|0 PERI:(DE-600)2406159-1
|n 15
|p 261-268
|t Deutsches Ärzteblatt international
|v 120
|y 2023
|x 1866-0452
909 C O |o oai:inrepo02.dkfz.de:277884
|p VDB
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 0
|6 P:(DE-HGF)0
913 1 _ |a DE-HGF
|b Programmungebundene Forschung
|l ohne Programm
|1 G:(DE-HGF)POF4-890
|0 G:(DE-HGF)POF4-899
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-800
|4 G:(DE-HGF)POF
|v ohne Topic
|x 0
914 1 _ |y 2023
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2022-11-18
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2022-11-18
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b DTSCH ARZTEBL INT : 2022
|d 2023-08-19
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2023-08-19
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2023-08-19
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0320
|2 StatID
|b PubMed Central
|d 2023-08-19
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2023-08-19
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2023-08-19
915 _ _ |a IF >= 5
|0 StatID:(DE-HGF)9905
|2 StatID
|b DTSCH ARZTEBL INT : 2022
|d 2023-08-19
920 1 _ |0 I:(DE-He78)ED01-20160331
|k ED01
|l DKTK Koordinierungsstelle Essen/Düsseldorf
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)ED01-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21