A new conditioning regimen involving total marrow irradiation, busulfan and cyclophosphamide followed by autologous PBSCT in patients with advanced multiple myeloma

被引:33
作者
Einsele, H
Bamberg, M
Budach, W
Schmidberger, H
Hess, CF
Wörmann, B
Meisner, C
Straka, C
Hebart, H
Trümper, L
Kröger, N
Zander, AR
Hegewisch-Becker, S
Hossfeld, DK
Schmidt, H
Müller, P
Schlimok, G
Hertenstein, B
Peest, D
Metzner, B
Frickhofen, N
Kanz, L
Bensinger, WI
机构
[1] Dept Hematol & Oncol, Tubingen, Germany
[2] Dept Radiotherapy, Tubingen, Germany
[3] Dept Radiotherapy, Gottingen, Germany
[4] Dept Hematol & Oncol, Gottingen, Germany
[5] Inst Med Informat Proc, Tubingen, Germany
[6] City Hosp, Dept Hematol, Munich, Germany
[7] Dept Hematol Oncol, Homburg, Germany
[8] Dept Hematol Oncol, Hamburg, Germany
[9] Dept Hematol Oncol, Augsburg, Germany
[10] Dept Hematol Oncol, Hannover, Germany
[11] Dept Hematol Oncol, Oldenburg, Germany
[12] Dept Hematol Oncol, Ulm, Germany
[13] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
关键词
multiple myeloma; high-dose therapy; total marrow irradiation; busulfan and cyclophosphamide; stem cell transplantation;
D O I
10.1038/sj.bmt.1704192
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The overall survival of patients with advanced multiple myeloma (MM) undergoing high-dose chemotherapy and autologous stem cell transplantation (SCT) depends mainly on the quality of response. Thus, to improve the response rate, a new intensified high-dose chemoradio-therapy was evaluated in a phase I/II study. After induction chemotherapy, 89 patients (median age 51 years, range 32-60 years) with MM stage II/III received a conditioning regimen with total marrow irradiation (9 Gy), busulfan (12 mg/kg) and cyclophosphamide (120 mg/kg) followed by SCT. Regimen-related toxicity according to WHO criteria and response rates defined by EBMT/IBMTR were analyzed. The main toxicity was mucositis grade III/IV in 76%, and fever grade >I in 75% of patients. Three patients developed reversible veno-occlusive disease. Transplant-related mortality was 2%. Among patients with de novo and pretreated MM, a CR rate of 48 and 41%, respectively, was documented. With a median follow-up of 45 months, the actuarial median durations of event-free survival (EFS) and overall survival (OS) after transplant were 29 and 61 months for the whole group, 36 and 85 months for patients with de novo MM, respectively. Thus, administration of this intensified conditioning regimen was associated with tolerable toxicity, a high response rate and long EFS and OS.
引用
收藏
页码:593 / 599
页数:7
相关论文
共 30 条
[1]   EARLY MYELOABLATIVE THERAPY FOR MULTIPLE-MYELOMA [J].
ALEXANIAN, R ;
DIMOPOULOS, MA ;
HESTER, J ;
DELASALLE, K ;
CHAMPLIN, R .
BLOOD, 1994, 84 (12) :4278-4282
[2]   A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma [J].
Attal, M ;
Harousseau, JL ;
Stoppa, AM ;
Sotto, JJ ;
Fuzibet, JG ;
Rossi, JF ;
Casassus, P ;
Maisonneuve, H ;
Facon, T ;
Ifrah, N ;
Payen, C ;
Bataille, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (02) :91-97
[3]  
BARLOGIE B, 1986, BLOOD, V67, P1298
[4]   Superiority of tandem autologous transplantation over standard therapy for previously untreated multiple myeloma [J].
Barlogie, B ;
Jagannath, S ;
Vesole, DH ;
Naucke, S ;
Cheson, B ;
Mattox, S ;
Bracy, D ;
Salmon, S ;
Jacobson, J ;
Crowley, J ;
Tricot, G .
BLOOD, 1997, 89 (03) :789-793
[5]   Total therapy with tandem transplants for newly diagnosed multiple myeloma [J].
Barlogie, B ;
Jagannath, S ;
Desikan, KR ;
Mattox, S ;
Vesole, D ;
Siegel, D ;
Tricot, G ;
Munshi, N ;
Fassas, A ;
Singhal, S ;
Mehta, J ;
Anaissie, E ;
Dhodapkar, D ;
Naucke, S ;
Cromer, J ;
Sawyer, J ;
Epstein, J ;
Spoon, D ;
Ayers, D ;
Cheson, B ;
Crowley, J .
BLOOD, 1999, 93 (01) :55-65
[6]  
BARLOGIE B, 1995, HEMATOLOGY WILLIAMS, P1109
[7]   High-dose therapy followed by autologous hematopoietic stem-cell infusion for patients with multiple myeloma [J].
Bensinger, WI ;
Rowley, SD ;
Demirer, T ;
Lilleby, K ;
Schiffman, K ;
Clift, RA ;
Appelbaum, FR ;
Fefer, A ;
Barnett, T ;
Storb, R ;
Chauncey, T ;
Maziarz, RT ;
Klarnet, J ;
McSweeney, P ;
Holmberg, L ;
Maloney, DG ;
Weaver, CH ;
Buckner, CD .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (05) :1447-1456
[8]  
Blade Joan, 1998, British Journal of Haematology, V102, P1115, DOI 10.1046/j.1365-2141.1998.00930.x
[9]   MULTIPLE-MYELOMA - VMCP/VBAP ALTERNATING COMBINATION CHEMOTHERAPY IS NOT SUPERIOR TO MELPHALAN AND PREDNISONE EVEN IN HIGH-RISK PATIENTS [J].
BOCCADORO, M ;
MARMONT, F ;
TRIBALTO, M ;
AVVISATI, G ;
ANDRIANI, A ;
BARBUI, T ;
CANTONETTI, M ;
CAROTENUTO, M ;
COMOTTI, B ;
DAMMACCO, F ;
FRIERI, R ;
GALLAMINI, A ;
GALLONE, G ;
GIOVANGROSSI, P ;
GRIGNANI, F ;
LAUTA, VM ;
LIBERATI, M ;
MUSTO, P ;
NERETTO, G ;
PETRUCCI, MT ;
RESEGOTTI, L ;
PILERI, A ;
MANDELLI, F .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (03) :444-448
[10]   Diagnosis, prognosis, and standard treatment of multiple myeloma [J].
Boccadoro, M ;
Pileri, A .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1997, 11 (01) :111-&