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Verfasst von:Schetelig, Johannes [VerfasserIn]   i
 Dreger, Peter [VerfasserIn]   i
Titel:Risk factors for treatment failure after allogeneic transplantation of patients with CLL
Titelzusatz:a report from the European Society for Blood and Marrow Transplantation
Verf.angabe:J. Schetelig, L.C. de Wreede, M. van Gelder, N.S. Andersen, C. Moreno, A. Vitek, M. Karas, M. Michallet, M. Machaczka, M. Gramatzki, D. Beelen, J. Finke, J. Delgado, L. Volin, J. Passweg, P. Dreger, A. Henseler, A. van Biezen, M. Bornhäuser, S. O. Schönland and N. Kröger on behalf of the CLL subcommittee, Chronic Malignancies Working Party
Umfang:9 S.
Fussnoten:Gesehen am 23.04.2018
Titel Quelle:Enthalten in: Bone marrow transplantation
Jahr Quelle:2017
Band/Heft Quelle:52(2017), 4, S. 552-560
ISSN Quelle:1476-5365
Abstract:For young patients with high-risk CLL, BTK-/PI3K-inhibitors or allogeneic stem cell transplantation (alloHCT) are considered. Patients with a low risk of non-relapse mortality (NRM) but a high risk of failure of targeted therapy may benefit most from alloHCT. We performed Cox regression analyses to identify risk factors for 2-year NRM and 5-year event-free survival (using EFS as a surrogate for long-term disease control) in a large, updated EBMT registry cohort (n= 694). For the whole cohort, 2-year NRM was 28% and 5-year EFS 37%. Higher age, lower performance status, unrelated donor type and unfavorable sex-mismatch had a significant adverse impact on 2-year NRM. Two-year NRM was calculated for good- and poor-risk reference patients. Predicted 2-year-NRM was 11 and 12% for male and female good-risk patients compared with 42 and 33% for male and female poor-risk patients. For 5-year EFS, age, performance status, prior autologous HCT, remission status and sex-mismatch had a significant impact, whereas del(17p) did not. The model-based prediction of 5-year EFS was 55% and 64%, respectively, for male and female good-risk patients. Good-risk transplant candidates with high-risk CLL and limited prognosis either on or after failure of targeted therapy should still be considered for alloHCT.
DOI:doi:10.1038/bmt.2016.329
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.

Verlag: http://dx.doi.org/10.1038/bmt.2016.329
 Verlag: https://www.nature.com/articles/bmt2016329
 DOI: https://doi.org/10.1038/bmt.2016.329
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1572257458
Verknüpfungen:→ Zeitschrift

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