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Verfasst von:Schlenk, Richard Friedrich [VerfasserIn]   i
 Müller-Tidow, Carsten [VerfasserIn]   i
 Benner, Axel [VerfasserIn]   i
 Kieser, Meinhard [VerfasserIn]   i
Titel:Relapsed/refractory acute myeloid leukemia
Titelzusatz:any progress?
Verf.angabe:Richard F. Schlenk, Carsten Müller-Tidow, Axel Benner, and Meinhard Kieser
Jahr:2017
Umfang:7 S.
Fussnoten:Gesehen am 11.05.2018
Titel Quelle:Enthalten in: Current opinion in oncology
Ort Quelle:Philadelphia, Pa. : Lippincott Williams & Wilkins, 1989
Jahr Quelle:2017
Band/Heft Quelle:29(2017), 6, Seite 467-473
ISSN Quelle:1531-703X
Abstract:Aim of this review was to focus on prognostic and predictive factors, standard and new treatment approaches, and on statistical considerations for future clinical trials in patients with relapsed/refractory acute myeloid leukemia (r/r-AML). New prognostic molecular markers were identified in r/r-AML, FLT3-ITD, mutated IDH1, and biallelic CEBPA mutations. Intensive combination chemotherapy including gemtuzumab ozogamicin emerged as an effective salvage therapy in refractory AML. Timing of allo-HCT in r/r-AML may be oriented at the probability to achieve a response to intensive salvage therapy. Several new treatment approaches ranging from new and modified cytotoxic drugs to targeted approaches are in clinical development with first efficacy assessment in single-arm phase II studies. Their external validity may be considerably increased by using a novel design based on a matching approach. FLT3-ITD, mutated IDH1, and biallelic CEBPA mutations are identified as prognostic molecular markers in r/r-AML. Timing of allo-HCT should be based on the probability to achieve a response to intensive salvage therapy. Several new approaches are currently evaluated and matching for controls may help to increase external validity.
DOI:doi:10.1097/CCO.0000000000000404
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: http://dx.doi.org/10.1097/CCO.0000000000000404
 Volltext: https://insights.ovid.com/pubmed?pmid=28857842
 DOI: https://doi.org/10.1097/CCO.0000000000000404
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1574984020
Verknüpfungen:→ Zeitschrift

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