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Verfasst von:Kröger, Nicolaus [VerfasserIn]   i
 Sockel, Katja [VerfasserIn]   i
 Wolschke, Christine [VerfasserIn]   i
 Bethge, Wolfgang [VerfasserIn]   i
 Schlenk, Richard Friedrich [VerfasserIn]   i
 Wolf, Dominik [VerfasserIn]   i
 Stadler, Michael [VerfasserIn]   i
 Kobbe, Guido [VerfasserIn]   i
 Wulf, Gerald [VerfasserIn]   i
 Bug, Gesine [VerfasserIn]   i
 Schäfer-Eckart, Kerstin [VerfasserIn]   i
 Scheid, Christof [VerfasserIn]   i
 Nolte, Florian [VerfasserIn]   i
 Krönke, Jan [VerfasserIn]   i
 Stelljes, Matthias [VerfasserIn]   i
 Beelen, Dietrich [VerfasserIn]   i
 Heinzelmann, Marion [VerfasserIn]   i
 Haase, Detlef [VerfasserIn]   i
 Buchner, Hannes [VerfasserIn]   i
 Bleckert, Gabriele [VerfasserIn]   i
 Giagounidis, Aristoteles [VerfasserIn]   i
 Platzbecker, Uwe [VerfasserIn]   i
Titel:Comparison between 5-azacytidine treatment and allogeneic stem-cell transplantation in elderly patients with advanced MDS according to donor availability (VidazaAllo Study)
Verf.angabe:Nicolaus Kröger, MD; Katja Sockel, MD; Christine Wolschke, MD; Wolfgang Bethge, MD; Richard F. Schlenk, MD, Dominik Wolf, MD; Michael Stadler, MD; Guido Kobbe, MD; Gerald Wulf, MD; Gesine Bug, MD; Kerstin Schäfer-Eckart, MD; Christof Scheid, MD; Florian Nolte, MD; Jan Krönke, MD; Matthias Stelljes, MD; Dietrich Beelen, MD; Marion Heinzelmann; Detlef Haase, MD; Hannes Buchner, PhD; Gabriele Bleckert, PhD; Aristoteles Giagounidis, MD; Uwe Platzbecker, MD; on behalf of the German MDS Study Group and the German Cooperative Transplant Study Group
E-Jahr:2021
Jahr:July 20, 2021
Umfang:11 S.
Fussnoten:Gesehen am 25.03.2022
Titel Quelle:Enthalten in: Journal of clinical oncology
Ort Quelle:Alexandria, Va. : American Society of Clinical Oncology, 1983
Jahr Quelle:2021
Band/Heft Quelle:39(2021), 30, Seite 3318-3327
ISSN Quelle:1527-7755
Abstract:PURPOSE - - In contrast to 5-azacytidine (5-aza), allogeneic stem-cell transplantation (HSCT) represents a curative treatment strategy for patients with myelodysplastic syndromes (MDS), but therapy-related mortality (TRM) limits its broader use in elderly patients with MDS. The present prospective multicenter study compared HSCT following 5-aza pretreatment with continuous 5-aza treatment in patients with higher-risk MDS age 55-70 years. - - METHODS - - One hundred ninety patients with a median age of 63 years were enrolled. Patients received 4-6 cycles of 5-aza followed by HLA-compatible HSCT after reduced-intensity conditioning or by continuous 5-aza if no donor was identified. - - RESULTS - - Twenty-eight patients did not fulfill inclusion criteria (n = 20), died (n = 2) withdrew informed consent (n = 5), or were excluded for an unknown reason (n = 1). 5-aza induction started in 162 patients, but only 108 (67%) were eligible for subsequent allocation to HSCT (n = 81) or continuation of 5-aza (n = 27) because of disease progression (n = 26), death (n = 12), or other reasons (n = 16). Seven percent died during 5-aza before treatment allocation. The cumulative incidence of TRM after HSCT at 1 year was 19%. The event-free survival and overall survival after 5-aza pretreatment and treatment allocation at 3 years were 34% (95% CI, 22 to 47) and 50% (95% CI, 39 to 61) after allograft and 0% and 32% (95% CI, 14 to 52) after continuous 5-aza treatment (P < .0001 and P = .12), respectively. Fourteen patients progressing after continuous 5-aza received a salvage allograft from an alternative donor, and 43% were alive at last follow-up. - - CONCLUSION - - In older patients with MDS, reduced-intensity conditioning HSCT resulted in a significantly improved event-free survival in comparison with continuous 5-aza therapy. Bridging with 5-aza to HSCT before is associated with a considerable rate of dropouts because of progression, mortality, and adverse events.
DOI:doi:10.1200/JCO.20.02724
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1200/JCO.20.02724
 Volltext: https://ascopubs.org/doi/10.1200/JCO.20.02724
 DOI: https://doi.org/10.1200/JCO.20.02724
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1796681423
Verknüpfungen:→ Zeitschrift

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