Dose-dense induction with sequential high-dose cytarabine and mitoxantone (S-HAM) and pegfilgrastim results in a high efficacy and a short duration of critical neutropenia in de novo acute myeloid leukemia: a pilot study of the AMLCG

被引:51
作者
Braess, Jan [1 ]
Spiekermann, Karsten
Staib, Peter [2 ,3 ]
Grueneisen, Andreas [4 ]
Woermann, Bernhard [5 ]
Ludwig, Wolf-Dieter [6 ]
Serve, Hubert [7 ]
Reichle, Albrecht [8 ]
Peceny, Rudolf [9 ]
Oruzio, Daniel [10 ]
Schmid, Christoph [10 ]
Schiel, Xaver [11 ]
Hentrich, Marcus [11 ]
Sauerland, Christina [12 ]
Unterhalt, Michael
Fiegl, Michael
Kern, Wolfgang [13 ]
Buske, Christian
Bohlander, Stefan
Heinecke, Achim [12 ]
Baurmann, Herrad [14 ]
Beelen, Dietrich W. [15 ]
Berdel, Wolfgang E.
Buechner, Thomas [16 ]
Hiddemann, Wolfgang [16 ]
机构
[1] Univ Munich, Klinikum Grosshadern, Lab Leukemia Diagnost, Dept Internal Med 3, D-81377 Munich, Germany
[2] Univ Klinikum, Cologne, Germany
[3] St Antonius Hosp, Eschweiler, Germany
[4] Vivantes Klinikum Berlin Neukolln, Berlin, Germany
[5] Stadt Klinikum, Braunschweig, Germany
[6] Free Univ Berlin, Klinikum Rudolf Virchow, Robert Rossle Klin, D-13122 Berlin, Germany
[7] Klinikum JW Goethe Univ, Frankfurt, Germany
[8] Klinikum Univ, Regensburg, Germany
[9] Klinikum Osnabruck, Osnabruck, Germany
[10] Zent Klinikum, Augsburg, Germany
[11] Klinikum Harlaching, Stadt Klinikum Munchen, Munich, Germany
[12] Univ Munster, Inst Med Informat & Biomath, Munster, Germany
[13] MLL Munchner Leukamielabor, Munich, Germany
[14] Deutsch Klin Diagnost, D-6200 Wiesbaden, Germany
[15] Univ Klinikum Essen, Essen, Germany
[16] Univ Klinikum Munster, Munster, Germany
关键词
BONE-MARROW-TRANSPLANTATION; ACUTE NONLYMPHOCYTIC LEUKEMIA; ACUTE MYELOGENOUS LEUKEMIA; STEM-CELL TRANSPLANTATION; CYTOSINE-ARABINOSIDE; COOPERATIVE GROUP; INTENSIVE CHEMOTHERAPY; PROLONGED MAINTENANCE; EARLY INTENSIFICATION; 1ST REMISSION;
D O I
10.1182/blood-2008-07-162842
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dose density during early induction has been demonstrated to be one of the prime determinants for treatment efficacy in acute myeloid leukemia (AML). The German AML Cooperative Group has therefore piloted a dose-dense induction regimen sequential high-dose AraC and mitoxantrone followed by pegfilgrastim (S-HAM) in which 2 induction cycles are applied over 11 to 12 days instead of 25 to 29 days as used in conventional double induction, thereby increasing dose density 2-fold. Of 172 de novo AML patients (excluding acute promyelocytic leukemia), 61% reached a complete remission, 22% a complete remission with incomplete peripheral recovery, 7% had persistent leukemia, 10% died (early death) resulting in an overall response rate of 83%. Kaplan-Meier estimated survival at 2 years was 61% for the whole group (patients with unfavorable karyotypes, 38%; patients with favorable karyotypes, 69%; patients with intermediate karyotypes, 75%) after S-HAM treatment. Importantly, the compression of the 2 induction cycles into the first 11 to 12 days of treatment was beneficial for normal hematopoiesis as demonstrated by a significantly shortened duration of critical neutropenia of 31 days compared with 46 days after conventionally timed double induction. (European Leukemia Trial Registry LN_AMLINT_2004_230.) (Blood. 2009;113:3903-3910)
引用
收藏
页码:3903 / 3910
页数:8
相关论文
共 36 条
[1]  
ARCHIMBAUD E, 1991, BLOOD, V77, P1894
[2]  
BUCHNER T, 1991, SEMIN HEMATOL, V28, P76
[3]   Double induction containing either two courses or one course of high-dose cytarabine plus mitoxantrone and postremission therapy by either autologous stem-cell transplantation or by prolonged maintenance for acute myeloid leukemia [J].
Büchner, T ;
Berdel, WE ;
Schoch, C ;
Haferlach, T ;
Serve, HL ;
Kienast, J ;
Schnittger, S ;
Kern, W ;
Tchinda, J ;
Reichle, A ;
Lengfelder, E ;
Staib, P ;
Ludwig, WD ;
Aul, C ;
Eimermacher, H ;
Balleisen, L ;
Sauerland, MC ;
Heinecke, A ;
Wöermann, B ;
Hiddemann, W .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (16) :2480-2489
[4]  
Büchner T, 1999, BLOOD, V93, P4116
[5]   MULTICENTER STUDY ON INTENSIFIED REMISSION INDUCTION THERAPY FOR ACUTE MYELOID-LEUKEMIA [J].
BUCHNER, T ;
URBANITZ, D ;
EMMERICH, B ;
FISCHER, JT ;
FULLE, HH ;
HEINECKE, A ;
HOSSFELD, DK ;
KOEPPEN, KM ;
LABEDZKI, L ;
LOFFLER, H ;
NOWROUSIAN, MR ;
PFREUNDSCHUH, M ;
PRALLE, H ;
RUHL, H ;
WENDT, FC .
LEUKEMIA RESEARCH, 1982, 6 (06) :827-831
[6]  
BUCHNER T, 1992, LEUKEMIA, V6, P68
[7]  
BURKE PJ, 1977, CANCER RES, V37, P2138
[8]   Randomised comparison of addition of autologous bone-marrow transplantation to intensive chemotherapy for acute myeloid leukaemia in first remission: results of MRC AML 10 trial [J].
Burnett, AK ;
Goldstone, AH ;
Stevens, RMF ;
Hann, IM ;
Rees, JKH ;
Gray, RG ;
Wheatley, K .
LANCET, 1998, 351 (9104) :700-708
[9]   Chemotherapy compared with autologous or allogeneic bone marrow transplantation in the management of acute myeloid leukemia in first remission [J].
Cassileth, PA ;
Harrington, DP ;
Appelbaum, FR ;
Lazarus, HM ;
Rowe, JM ;
Paietta, E ;
Willman, C ;
Hurd, DD ;
Bennett, JM ;
Blume, KG ;
Head, DR ;
Wiernik, PH .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (23) :1649-1656
[10]   Randomized comparison of double induction and timed-sequential induction to a "3+7" induction in adults with AML:: long-term analysis of the Acute Leukemia French Association (ALFA) 9000 study [J].
Castaigne, S ;
Chevret, S ;
Archimbaud, E ;
Fenaux, P ;
Bordessoule, D ;
Tilly, H ;
de Revel, T ;
Simon, M ;
Dupriez, B ;
Renoux, M ;
Janvier, M ;
Micléa, JM ;
Thomas, X ;
Bastard, C ;
Preudhomme, C ;
Bauters, F ;
Degos, L ;
Dombret, H .
BLOOD, 2004, 104 (08) :2467-2474