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@ARTICLE{Walther:307536,
author = {D. Walther and J. Ernst and C. Wollenhaupt and S. Wittig
and M. Härtel and G. Brodt and T. Milde$^*$ and B. Gruhn},
title = {{E}fficacy and {S}afety of {D}onor {L}ymphocyte {I}nfusion
{A}fter {A}llogeneic {H}ematopoietic {S}tem {C}ell
{T}ransplantation in {P}ediatric {P}atients.},
journal = {European journal of haematology},
volume = {nn},
issn = {0902-4441},
address = {Oxford},
publisher = {Wiley-Blackwell},
reportid = {DKFZ-2026-00041},
pages = {nn},
year = {2026},
note = {epub},
abstract = {This retrospective study evaluates the efficacy and safety
of donor lymphocyte infusion (DLI) after allogeneic
hematopoietic stem cell transplantation (HSCT) in children.
We describe the long-term use of preemptive, prophylactic,
and therapeutic DLI with a gradual dose increase in half-log
increments. Under close monitoring, we increased the DLI
dose only in patients that did not show signs of
graft-versus-host disease (GVHD). In the preemptive cohort,
10 of 12 patients $(83\%)$ with minimal residual disease
(MRD) positivity remained relapse-free. Among 11 patients
with genetic diseases and mixed chimerism, nine $(82\%)$
responded to preemptive DLI. Six patients $(100\%)$ of the
prophylactic cohort with a very high risk of relapse had a
successful outcome without relapse or GVHD. Three of the
five patients $(60\%)$ of the therapeutic cohort were
successfully treated with DLI. We observed acute GVHD (grade
I and II) in only two patients $(6\%).$ The results of our
study indicate that the long-term use of DLI is a promising
strategy and can effectively prevent relapse, graft
rejection, and even cure relapse. The observed low rate of
GVHD may be attributed to the gradual dose increase.
Therefore, we consider DLI a safe and effective therapeutic
option.},
keywords = {donor chimerism (Other) / donor lymphocyte infusion (Other)
/ graft‐versus‐host disease (Other) /
graft‐versus‐leukemia effect (Other) / hematopoietic
stem cell transplantation (Other)},
cin = {B310},
ddc = {610},
cid = {I:(DE-He78)B310-20160331},
pnm = {312 - Funktionelle und strukturelle Genomforschung
(POF4-312)},
pid = {G:(DE-HGF)POF4-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:41489018},
doi = {10.1111/ejh.70112},
url = {https://inrepo02.dkfz.de/record/307536},
}