Dose-escalated CHOP plus etoposide (MegaCHOEP) followed by repeated stem cell transplantation for primary treatment of aggressive high-risk non-Hodgkin lymphoma

被引:51
作者
Glass, B
Kloess, M
Bentz, M
Schlimok, G
Berdel, WE
Feller, A
Trümper, L
Loeffler, M
Pfreundschuh, M
Schmitz, N
机构
[1] Univ Groningen Hosp, Dept Hematol & Oncol, D-37075 Gottingen, Germany
[2] Univ Leipzig, Inst Med Informat Stat & Epidemiol, D-7010 Leipzig, Germany
[3] Community Hosp Karlsruhe, Dept Hematol & Oncol, Karlsruhe, Germany
[4] Klinikum Augsburgaug, Dept Internal Med 2, Augsburg, Germany
[5] Univ Munster, Dept Internal Med A, D-4400 Munster, Germany
[6] Univ Schleswig Holstein, Inst Pathol, Lubeck, Germany
[7] Univ Saarland, Sch Med, Hosp Med, D-6650 Homburg, Germany
[8] Asklepios Klin St Georg, Dept Hematol, Hamburg, Germany
关键词
D O I
10.1182/blood-2005-04-1570
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Feasibility, safety, and efficacy of a 4-course high-dose chemotherapy (HDT) protocol including autologous stem cell transplantation (SCT) after courses 2, 3, and 4 was investigated in 110 patients, aged 18 to 60 years, with primary diagnosis of aggressive NHL (aNHL), and lactic dehydrogenase (LDH) levels above normal. At dose level 1 (DL1), course 1 consisted of cyclophosphamide 1500 mg/m(2), doxorubicin (Adriamycin) 70 mg/m(2), vincristine 2 mg, etoposide 450 mg/m(2), and prednisone 500 mg. With courses 2 and 3 cyclophosphamide and etoposide were escalated to 4500 mg/m(2) and 600 mg/m(2), respectively. With course 4 cyclophosphamide and etoposide were given at 6000 mg/m(2) and 1000 mg/m(2), respectively. At DL2 etoposide was further increased to 600, 960, 960, and 1480 mg/m(2) with courses 1 to 4, respectively. Therapy as per protocol was completed by 81.8% of patients. Overall survival at 5 years was 67.2%, freedom from treatment failure (FFTF) was 62.1%, and treatment-related mortality was 4.5%. There was a trend to better FFTF at DL2 compared to DL1 (66.9% versus 54.2%). Repetitive HDT with escalated CHOP plus etoposide is feasible and effective treatment of patients with aNHL. DL2 of this therapy is being used in an ongoing phase 3 study.
引用
收藏
页码:3058 / 3064
页数:7
相关论文
共 28 条
[1]
REGIMEN-RELATED TOXICITY IN PATIENTS UNDERGOING BONE-MARROW TRANSPLANTATION [J].
BEARMAN, SI ;
APPELBAUM, FR ;
BUCKNER, CD ;
PETERSEN, FB ;
FISHER, LD ;
CLIFT, RA ;
THOMAS, ED .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (10) :1562-1568
[2]
Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas [J].
Cheson, BD ;
Horning, SJ ;
Coiffier, B ;
Shipp, MA ;
Fisher, RI ;
Connors, JM ;
Lister, TA ;
Vose, J ;
Grillo-López, A ;
Hagenbeek, A ;
Cabanillas, F ;
Klippensten, D ;
Hiddemann, W ;
Castellino, R ;
Harris, NL ;
Armitage, JO ;
Carter, W ;
Hoppe, R ;
Canellos, GP .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1244-1253
[3]
del Cañizo C, 1999, BONE MARROW TRANSPL, V23, P901
[4]
COMPARISON OF A STANDARD REGIMEN (CHOP) WITH 3 INTENSIVE CHEMOTHERAPY REGIMENS FOR ADVANCED NON-HODGKINS-LYMPHOMA [J].
FISHER, RI ;
GAYNOR, ER ;
DAHLBERG, S ;
OKEN, MM ;
GROGAN, TM ;
MIZE, EM ;
GLICK, JH ;
COLTMAN, CA ;
MILLER, TP .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (14) :1002-1006
[5]
High-dose chemotherapy and autologous bone marrow transplantation compared with MACOP-B in aggressive B-cell lymphoma [J].
Gianni, AM ;
Bregni, M ;
Siena, S ;
Brambilla, C ;
DiNicola, M ;
Lombardi, F ;
Gandola, L ;
Tarella, C ;
Pileri, A ;
Ravagnani, F ;
Valagussa, P ;
Bonadonna, G ;
Stern, AC ;
Magni, M ;
Caracciolo, D .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (18) :1290-1297
[6]
Shortened first-line high-dose chemotherapy for patients with poor-prognosis aggressive lymphoma [J].
Gisselbrecht, C ;
Lepage, E ;
Molina, T ;
Quesnel, B ;
Fillet, G ;
Lederlin, P ;
Coiffier, B ;
Tilly, H ;
Gabarre, J ;
Guilmin, F ;
Hermine, O ;
Reyes, F .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (10) :2472-2479
[7]
Benefit of autologous bone marrow transplantation over sequential chemotherapy in poor-risk aggressive non-Hodgkin's lymphoma: Updated results of the prospective study LNH87-2 [J].
Haioun, C ;
Lepage, E ;
Gisselbrecht, C ;
Bastion, Y ;
Coiffier, B ;
Brice, P ;
Bosly, A ;
Dupriez, B ;
Nouvel, C ;
Tilly, H ;
Lederlin, P ;
Biron, P ;
Briere, J ;
Gaulard, P ;
Reyes, F .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (03) :1131-1137
[8]
Survival benefit of high-dose therapy in poor-risk aggressive non-Hodgkin's lymphoma:: Final analysis of the prospective LNH87-2 protocol -: A Groupe d'Etude des Lymphomes de l'Adulte Study [J].
Haioun, C ;
Lepage, E ;
Gisselbrecht, C ;
Salles, G ;
Coiffier, B ;
Brice, P ;
Bosly, A ;
Morel, P ;
Nouvel, C ;
Tilly, H ;
Lederlin, P ;
Sebban, C ;
Brière, J ;
Gaulard, P ;
Reyes, F .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (16) :3025-3030
[9]
Juliusson G, 1996, ANN ONCOL, V7, P1037
[10]
Randomized study to evaluate the use of high-dose therapy as part of primary treatment for "aggressive" lymphoma [J].
Kaiser, U ;
Uebelacker, L ;
Abel, U ;
Birkmann, J ;
Trümper, L ;
Schmalenberg, H ;
Karakas, T ;
Metzner, B ;
Hossfeld, DK ;
Bischoff, HG ;
Franke, A ;
Reiser, M ;
Müller, P ;
Mantovani, L ;
Grundeis, M ;
Rothmann, F ;
von Seydewitz, CU ;
Mesters, RM ;
Steinhauer, EU ;
Krahl, D ;
Schumacher, K ;
Kneba, M ;
Baudis, M ;
Schmitz, N ;
Pfab, R ;
Köppler, H ;
Parwaresch, R ;
Pfreundschuh, M ;
Havemann, K .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (22) :4413-4419