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Sequential high-dose cytarabine and mitoxantrone (S-HAM) versus standard double induction in acute myeloid leukemia-a phase 3 study.
Braess, Jan; Amler, Susanne; Kreuzer, Karl-Anton; Spiekermann, Karsten; Lindemann, Hans Walter; Lengfelder, Eva; Graeven, Ullrich; Staib, Peter; Ludwig, Wolf-Dieter; Biersack, Harald; Ko, Yon-Dschun; Uppenkamp, Michael J; De Wit, Maike; Korsten, Stefan; Peceny, Rudolf; Gaska, Tobias; Schiel, Xaver; Behringer, Dirk M; Kiehl, Michael G; Zinngrebe, Bettina; Meckenstock, Gerald; Roemer, Eva; Medgenberg, Dirk; Spaeth-Schwalbe, Ernst; Massenkeil, Gero; Hindahl, Heidrun; Schwerdtfeger, Rainer; Trenn, Guido; Sauerland, Cristina; Koch, Raphael; Lablans, Martin; Faldum, Andreas; Görlich, Dennis; Bohlander, Stefan K; Schneider, Stephanie; Dufour, Annika; Buske, Christian; Fiegl, Michael; Subklewe, Marion; Braess, Birgit; Unterhalt, Michael; Baumgartner, Anja; Wörmann, Bernhard; Beelen, Dietrich; Hiddemann, Wolfgang.
Afiliação
  • Braess J; Department of Oncology and Hematology, Hospital Barmherzige Brüder, Regensburg, Germany. Jan.Braess@barmherzige-regensburg.de.
  • Amler S; Department of Medicine III, University Hospital LMU Campus Grosshadern, Munich, Germany. Jan.Braess@barmherzige-regensburg.de.
  • Kreuzer KA; Insitute for Biostatistics and Clinical Research, University Hospital, Münster, Germany.
  • Spiekermann K; Friedrich Löffler Institute, Federal Research Centre, Greifswald-Insel Riems, Germany.
  • Lindemann HW; Department of Internal Medicine I, University Hospital, Cologne, Germany.
  • Lengfelder E; Department of Medicine III, University Hospital LMU Campus Grosshadern, Munich, Germany.
  • Graeven U; Department of Hematology and Oncology, Catholic Hospital, Hagen, Germany.
  • Staib P; Department of Medicine III, University Hospital, Mannheim, Germany.
  • Ludwig WD; Department of Medicine I, Hospital Maria Hilf, Mönchengladbach, Germany.
  • Biersack H; Department of Hematology and Medical Oncology, St. Antonius Hospital, Eschweiler, Germany.
  • Ko YD; Department of Hematology and Oncology and Tumor Immunology, Helios Hospital, Berlin-Buch, Germany.
  • Uppenkamp MJ; Department of Medicine I, University Hospital, Lübeck, Germany.
  • De Wit M; Department of Medicine I, Johanniter Hospital, Bonn, Germany.
  • Korsten S; Department of Medicine A, Klinikum Ludwigshafen, Ludwigshafen, Germany.
  • Peceny R; Department of Hematology, Oncology and Palliative Care, Vivantes Klinikum Neukölln, Berlin, Germany.
  • Gaska T; Department of Medicine, Vinzenz Pallotti Hospital, Bergisch-Gladbach, Germany.
  • Schiel X; Department of Hematology and Oncology, Klinikum Osnabrück, Osnabrück, Germany.
  • Behringer DM; Department of Hematology and Oncology, St. Josef Hospital, Paderborn, Germany.
  • Kiehl MG; Department of Hematology and Oncology, Klinikum Harlaching, Munich, Germany.
  • Zinngrebe B; Department of Hematology, Oncology and Palliative Care, Augusta Hospital, Bochum, Germany.
  • Meckenstock G; Department of Medicine I, Klinikum Frankfurt/Oder, Frankfurt/Oder, Germany.
  • Roemer E; Department of Hematology, Oncology and Palliative Care, Evangelisches Krankenhaus, Bielefeld, Germany.
  • Medgenberg D; Department of Medical Oncology, Radiooncology, Hematology and Palliative Care, St. Josef Hospital, Gelsenkirchen, Germany.
  • Spaeth-Schwalbe E; Department of Hematology and Oncology, Klinikum Idar-Oberstein, Idar-Oberstein, Germany.
  • Massenkeil G; Department of Medicine III, Klinikum Leverkusen, Leverkusen, Germany.
  • Hindahl H; Department of Medicine, Vivantes Klinikum Spandau, Berlin, Germany.
  • Schwerdtfeger R; Department of Medicine II, Klinikum Gütersloh, Gütersloh, Germany.
  • Trenn G; Department of Medicine I, St. Johannes Hospital, Dortmund, Germany.
  • Sauerland C; Department for Bone Marrow and Blood Stem Cell Transplantation, DKD Deutsche Klinik für Diagnostik, Wiesbaden, Germany.
  • Koch R; Department of Medicine I, Knappschaftskrankenhaus, Bottrop, Germany.
  • Lablans M; Insitute for Biostatistics and Clinical Research, University Hospital, Münster, Germany.
  • Faldum A; Insitute for Biostatistics and Clinical Research, University Hospital, Münster, Germany.
  • Görlich D; Insitute for Biostatistics and Clinical Research, University Hospital, Münster, Germany.
  • Bohlander SK; Division of Medical Informatics in Translational Oncology, DKFZ German Cancer Research Center, Heidelberg, Germany.
  • Schneider S; Insitute for Biostatistics and Clinical Research, University Hospital, Münster, Germany.
  • Dufour A; Insitute for Biostatistics and Clinical Research, University Hospital, Münster, Germany.
  • Buske C; Department of Medicine III, University Hospital LMU Campus Grosshadern, Munich, Germany.
  • Fiegl M; Department of Molecular Medicine and Pathology, University of Auckland, Auckland, New Zealand.
  • Subklewe M; Department of Medicine III, University Hospital LMU Campus Grosshadern, Munich, Germany.
  • Braess B; Department of Medicine III, University Hospital LMU Campus Grosshadern, Munich, Germany.
  • Unterhalt M; Department of Medicine III, University Hospital LMU Campus Grosshadern, Munich, Germany.
  • Baumgartner A; Institute of Experimental Cancer Research, University Hospital, Ulm, Germany.
  • Wörmann B; Department of Medicine III, University Hospital LMU Campus Grosshadern, Munich, Germany.
  • Beelen D; Department of Medicine III, University Hospital LMU Campus Grosshadern, Munich, Germany.
  • Hiddemann W; Department of Oncology and Hematology, Hospital Barmherzige Brüder, Regensburg, Germany.
Leukemia ; 32(12): 2558-2571, 2018 12.
Article em En | MEDLINE | ID: mdl-30275528
ABSTRACT
Dose-dense induction with the S-HAM regimen was compared to standard double induction therapy in adult patients with newly diagnosed acute myeloid leukemia. Patients were centrally randomized (11) between S-HAM (2nd chemotherapy cycle starting on day 8 = "dose-dense") and double induction with TAD-HAM or HAM(-HAM) (2nd cycle starting on day 21 = "standard"). 387 evaluable patients were randomly assigned to S-HAM (N = 203) and to standard double induction (N = 184). The primary endpoint overall response rate (ORR) consisting of complete remission (CR) and incomplete remission (CRi) was not significantly different (P = 0.202) between S-HAM (77%) and double induction (72%). The median overall survival was 35 months after S-HAM and 25 months after double induction (P = 0.323). Duration of critical leukopenia was significantly reduced after S-HAM (median 29 days) versus double induction (median 44 days)-P < 0.001. This translated into a significantly shortened duration of hospitalization after S-HAM (median 37 days) as compared to standard induction (median 49 days)-P < 0.001. In conclusion, dose-dense induction therapy with the S-HAM regimen shows favorable trends but no significant differences in ORR and OS compared to standard double induction. S-HAM significantly shortens critical leukopenia and the duration of hospitalization by 2 weeks.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Protocolos de Quimioterapia Combinada Antineoplásica / Mitoxantrona / Citarabina Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Protocolos de Quimioterapia Combinada Antineoplásica / Mitoxantrona / Citarabina Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article