Direkt zum Inhalt

Langer, Ronja ; Lelas, Antonela ; Rittenschober, Michael ; Piekarska, Agnieszka ; Sadowska-Klasa, Alicja ; Sabol, Ivan ; Desnica, Lana ; Greinix, Hildegard ; Dickinson, Anne ; Inngjerdingen, Marit ; Lawitschka, Anita ; Vrhovac, Radovan ; Pulanic, Drazen ; Güneş, Sibel ; Klein, Stefan ; Moritz Middeke, Jan ; Grube, Matthias ; Edinger, Matthias ; Herr, Wolfgang ; Wolff, Daniel

Retrospective analysis of the incidence and outcome of late acute and chronic graft-versus-host disease—an analysis from transplant centers across Europe

Artikel

Langer, Ronja, Lelas, Antonela, Rittenschober, Michael, Piekarska, Agnieszka, Sadowska-Klasa, Alicja, Sabol, Ivan , Desnica, Lana, Greinix, Hildegard, Dickinson, Anne, Inngjerdingen, Marit, Lawitschka, Anita, Vrhovac, Radovan, Pulanic, Drazen, Güneş, Sibel, Klein, Stefan, Moritz Middeke, Jan, Grube, Matthias, Edinger, Matthias, Herr, Wolfgang und Wolff, Daniel (2024) Retrospective analysis of the incidence and outcome of late acute and chronic graft-versus-host disease—an analysis from transplant centers across Europe. Frontiers in Transplantation 3.

DOI zum Zitieren dieses Dokuments: 10.5283/epub.58608


Zusammenfassung

Introduction: Chronic graft-versus-host disease (cGvHD) is a serious late complication of allogeneic hematopoietic stem cell transplantation (allo-HSCT). Methods: This multicenter analysis determined the cumulative incidence (CI) of cGvHD and late acute GvHD (laGvHD) and its impact on transplantation-related mortality (TRM), relapse (R), and overall survival (OS) in 317 patients [296 adults, ...

Introduction: Chronic graft-versus-host disease (cGvHD) is a serious late complication of allogeneic hematopoietic stem cell transplantation (allo-HSCT).

Methods: This multicenter analysis determined the cumulative incidence (CI) of cGvHD and late acute GvHD (laGvHD) and its impact on transplantation-related mortality (TRM), relapse (R), and overall survival (OS) in 317 patients [296 adults, 21 pediatrics (<12 years of age)] who underwent their first allo-HSCT in 2017.

Results: The CI of laGvHD was 10.5% in adults and 4.8% in pediatrics, and the CI of cGvHD was 43.0% in all adult transplant patients and 50.2% in the adult at-risk cohort at the study end. The onset of cGvHD was de novo in 42.0% of patients, quiescent in 52.1%, and progressive in 5.9%. In adults, prophylactic use of antithymocyte globulin or posttransplant cyclophosphamide was associated with a significantly lower incidence of cGvHD (28.7%) vs. standard prophylaxis with calcineurin inhibitors (30.6%) and methotrexate/mycophenolate mofetil (58.4%) (all p < 0.01). TRM was significantly higher in patients with aGvHD (31.8%) vs. cGvHD (12.6%) and no GvHD (6.3%) (all p = 0.0001). OS in the adult at-risk cohort was significantly higher in patients with cGvHD (78.9%) vs. without (66.2%; p = 0.0022; HR 0.48) due to a significantly lower relapse rate (cGvHD: 14.5%; without cGvHD: 27.2%; p = 0.00016, HR 0.41). OS was also significantly higher in patients with mild (80.0%) and moderate (79.2%) cGvHD vs. without cGvHD (66.2%), excluding severe cGvHD (72.7%) (all p = 0.0214).

Discussion: The negative impact of severe cGvHD on OS suggests a focus on prevention of severe forms is warranted to improve survival and quality of life.



Beteiligte Einrichtungen


Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftFrontiers in Transplantation
VerlagFrontiers
Open Access ArtGold (mit APC - nicht UR)
Band3
Datum18 März 2024
Veröffentlichungsdatum04 Jul 2024 09:17
InstitutionenMedizin > Lehrstuhl für Innere Medizin III (Hämatologie und Internistische Onkologie)
Identifikationsnummer
WertTyp
10.3389/frtra.2024.1332181DOI
Stichwörter / Keywordschronic graft-versus-host disease (cGvHD), acute GvHD, aGvHD, stem cell transplantation, bone marrow transplantation
Dewey-Dezimal-Klassifikation600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenJa
URN der UB Regensburgurn:nbn:de:bvb:355-epub-586086
Dokumenten-ID58608

Bibliographische Daten exportieren

Nur für Besitzer und Autoren: Kontrollseite des Eintrags

nach oben