Salvage chemotherapy with R-DHAP in patients with relapsed or refractory non-Hodgkin lymphoma

This analysis reports on 72 patients with relapsed or refractory non-Hodgkin lymphoma who were treated with R-DHAP salvage chemotherapy regimen followed by high-dose chemotherapy and stem cell transplantation. The overall remission rate was 58.3%. Median time of follow-up was 28.7 months. Median pro...

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Hauptverfasser: Schirmbeck, Nadine (VerfasserIn) , Mey, Ulrich J. M. (VerfasserIn) , Olivieri, Attilio (VerfasserIn) , Ko, Yon-Dschun (VerfasserIn) , Kaiser, Ulrich (VerfasserIn) , Flieger, Dimitri (VerfasserIn) , Witzens-Harig, Mathias (VerfasserIn) , Schmidt-Wolf, Ingo G. H. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 16 Sep 2016
In: Cancer investigation
Year: 2016, Jahrgang: 34, Heft: 8, Pages: 361-372
ISSN:1532-4192
DOI:10.1080/07357907.2016.1212062
Online-Zugang:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1080/07357907.2016.1212062
Verlag, lizenzpflichtig, Volltext: https://www.tandfonline.com/doi/full/10.1080/07357907.2016.1212062
Volltext
Verfasserangaben:Nadine G.D. Schirmbeck, Ulrich J.M. Mey, Attilio Olivieri, Yon-Dschun Ko, Ulrich Kaiser, Dimitri Flieger, Mathias Witzens-Harig, Ingo G.H. Schmidt-Wolf
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Zusammenfassung:This analysis reports on 72 patients with relapsed or refractory non-Hodgkin lymphoma who were treated with R-DHAP salvage chemotherapy regimen followed by high-dose chemotherapy and stem cell transplantation. The overall remission rate was 58.3%. Median time of follow-up was 28.7 months. Median progression-free survival was 29 months, estimated median overall survival was 37 months. Within a matched pair analysis these results were compared to a group that received DHAP salvage therapy without rituximab showing similar overall response rates and better estimated five-year overall survival of 59.2% versus 43.5%. R-DHAP therapy was shown to be effective and feasible with acceptable toxicity.
Beschreibung:Gesehen am 14.05.2020
Beschreibung:Online Resource
ISSN:1532-4192
DOI:10.1080/07357907.2016.1212062