Cyclophosphamide plus dexamethasone is an efficient initial treatment before high-dose melphalan and autologous stem cell transplantation in patients with newly diagnosed multiple myeloma - Results of a randomized comparison with vincristine, doxorubicin, and dexamethasone

被引:29
作者
Mellqvist, Ulf-Henrik [1 ]
Lenhoff, Stig [2 ]
Johnsen, Hans E. [3 ]
Hjorth, Martin [4 ]
Holmberg, Erik [5 ]
Juliusson, Gunnar [2 ]
Tangen, Jon Magnus [6 ]
Westin, Jan [1 ]
机构
[1] Sahlgrens Univ Hosp, Dept Hematol, S-41345 Gothenburg, Sweden
[2] Univ Lund Hosp, Dept Hematol, S-22185 Lund, Sweden
[3] Aarhus Univ, Aalborg Hosp, Dept Hematol, Aalborg, Denmark
[4] Linkoping Hosp, Dept Internal Med, Linkoping, Sweden
[5] Sahlgrens Univ Hosp, Ctr Oncol, S-41345 Gothenburg, Sweden
[6] Ullevaal Univ Hosp, Dept Hematol, Oslo, Norway
关键词
event-free survival; multiple myeloma; initial therapy; autologous stem cell transplantation;
D O I
10.1002/cncr.23145
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Today, intensive therapy that includes high-close melphalan with autologous stein cell transplantation (ASCT) is considered standard therapy in younger patients with newly diagnosed myeloma. When the current trial was initiated, combined vincristine, doxorubicin, and dexamethasone (VAD) was the most commonly used induction therapy before ASCT and yielded rapid major responses without interfering with stein cell harvest. However, the administration of VAD demands a central venous access, and well-described toxicities are associated with the therapy. This randomized trial, which was initiated in 2001 by the Nordic Myeloma Study Group, was an attempt to bring a larger portion of patients to ASCT more quickly. METHODS. Patients were randomized to receive either 3 cycles of VAD or 2 courses of cyclophosphamide plus dexamethasone (Cy-Dex) (cyclophosphamide at a dose of 1000 mg/m(2) on Day 1 and dexamethasone at a dose of 40 mg per day on Days 1-4 and 9-12, repeated on Day 22) as initial therapy followed by stein cell mobilization, harvest, and finally ASCT. RESULTS. No significant difference was observed in the proportion of patients undergoing ASCT (VAD [86%] vs Cy-Dex [87%]). During the first 4 months after the initiation of therapy, the mortality rates were 5.8% for VAD and 1.9% for Cy-Dex (P =.08). The response rates after ASCT were comparable (partial response or better: VAD: 80% vs Cy-Dex: 81%). In both groups, the median event-free survival was 29 months, and the overall survival rate at 3 years was 75%. CONCLUSIONS. The current results indicated that Cy-Dex before ASCT has efficacy comparable to that of VAD. It also demonstrated that a short course of alkylater therapy using cyclophosphamide does not affect stem cell harvest or transplantation.
引用
收藏
页码:129 / 135
页数:7
相关论文
共 28 条
  • [1] ALEXANIAN R, 1983, BLOOD, V62, P572
  • [2] VAD-BASED REGIMENS AS PRIMARY-TREATMENT FOR MULTIPLE-MYELOMA
    ALEXANIAN, R
    BARLOGIE, B
    TUCKER, S
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 1990, 33 (02) : 86 - 89
  • [3] ALEXANIAN R, 1992, BLOOD, V80, P887
  • [4] Outcomes of autologous stem cell transplantation in patients with multiple myeloma who received dexamethasone-based nonmyelosuppressive induction therapy
    Anagnostopoulos, A
    Aleman, A
    Yang, Y
    Donato, M
    Weber, D
    Champlin, R
    Smith, T
    Alexanian, R
    Giralt, S
    [J]. BONE MARROW TRANSPLANTATION, 2004, 33 (06) : 623 - 628
  • [5] VAD CHEMOTHERAPY AS REMISSION INDUCTION FOR MULTIPLE-MYELOMA
    ANDERSON, H
    SCARFFE, JH
    RANSON, M
    YOUNG, R
    WIERINGA, GS
    MORGENSTERN, GR
    FITZSIMMONS, L
    RYDER, D
    [J]. BRITISH JOURNAL OF CANCER, 1995, 71 (02) : 326 - 330
  • [6] [Anonymous], 1998, J Clin Oncol, V16, P3832
  • [7] EFFECTIVE TREATMENT OF ADVANCED MULTIPLE-MYELOMA REFRACTORY TO ALKYLATING-AGENTS
    BARLOGIE, B
    SMITH, L
    ALEXANIAN, R
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (21) : 1353 - 1356
  • [8] Superiority of thalidomide and dexamethasone over vincristine-doxorubicin-dexamethasone (VAD) as primary therapy in preparation for autologous transplantation for multiple myeloma
    Cavo, M
    Zamagni, E
    Tosi, P
    Tacchetti, P
    Cellini, C
    Cangini, D
    de Vivo, A
    Testoni, N
    Nicci, C
    Terragna, C
    Grafone, T
    Perrone, G
    Ceccolini, M
    Tura, S
    Baccarani, M
    [J]. BLOOD, 2005, 106 (01) : 35 - 39
  • [9] Cavo M, 2002, HAEMATOLOGICA, V87, P934
  • [10] DREWINKO B, 1981, BLOOD, V57, P333