Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/116023
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dc.contributor.authorLübke, Johannes-
dc.contributor.authorChristen, Deborah-
dc.contributor.authorSchwaab, Juliana-
dc.contributor.authorKaiser, Anne-
dc.contributor.authorNaumann, Nicole-
dc.contributor.authorShoumariyeh, Khalid-
dc.contributor.authorJentzsch, Barbara Madlen-
dc.contributor.authorSockel, Katja-
dc.contributor.authorHennigs, Judith Marie-
dc.contributor.authorAyuk, Francis-
dc.contributor.authorStelljes, Matthias-
dc.contributor.authorHilgendorf, Inken-
dc.contributor.author[und viele weitere]-
dc.date.accessioned2024-05-13T12:01:27Z-
dc.date.available2024-05-13T12:01:27Z-
dc.date.issued2024-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/117977-
dc.identifier.urihttp://dx.doi.org/10.25673/116023-
dc.description.abstractWe identified 71 patients with AdvSM (aggressive SM [ASM], SM with an associated hematologic neoplasm [SM-AHN, e.g., acute myeloid leukemia, SM-AML], mast cell leukemia [MCL]) in two national registries (DRST/GREM) who received an allogeneic hematopoietic cell transplantation (alloHCT) performed in Germany from 1999–2021. Median overall survival (OS) of ASM/SM-AHN (n = 30, 45%), SM-AML (n = 28, 39%) and MCL ± AHN (n = 13, 19%) was 9.0, 3.3 and 0.9 years (P = 0.007). Improved median OS was associated with response of SM (17/41, 41%; HR 0.4 [0.2–0.9], P = 0.035) and/or of AHN (26/43, 60%, HR 0.3 [0.1–0.7], P = 0.004) prior to alloHCT. Adverse predictors for OS included absence of KIT D816V (10/61, 16%, HR 2.9 [1.2–6.5], P < 0.001) and a complex karyotype (9/60, 15%, HR 4.2 [1.8–10.0], P = 0.016). HLA-match, conditioning type or transplantation at centers reporting above-average alloHCTs (≥7) had no impact on OS. Taking into account competing events at years 1, 3 and 5, relapse-related mortality and non-relapse mortality rate were 15%/23%, 20%/30% and 23%/35%, respectively. Irrespective of subtype, subsequent treatment response was achieved in 13/30 (43%) patients and was highest on midostaurin/avapritinib (7/9, 78%). We conclude that outcome of alloHCT in AdvSM is more affected by disease phenotype and treatment response prior to transplant than by transplant characteristics.eng
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc610-
dc.titleAllogeneic hematopoietic cell transplantation in advanced Systemic mastocytosis : a retrospective analysis of the DRST and GREM registrieseng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleLeukemia-
local.bibliographicCitation.volume38-
local.bibliographicCitation.issue4-
local.bibliographicCitation.pagestart810-
local.bibliographicCitation.pageend821-
local.bibliographicCitation.publishernameSpringer Nature-
local.bibliographicCitation.publisherplaceLondon-
local.bibliographicCitation.doi10.1038/s41375-024-02186-x-
local.openaccesstrue-
dc.identifier.ppn1885704658-
cbs.publication.displayform2024-
local.bibliographicCitation.year2024-
cbs.sru.importDate2024-05-13T12:00:54Z-
local.bibliographicCitationEnthalten in Leukemia - London : Springer Nature, 1997-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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