Continuous low-dose cyclophosphamide-prednisone is effective and well tolerated in patients with advanced multiple myeloma

被引:30
作者
de Weerdt, O
van de Donk, NWCJ
Veth, G
Bloem, AC
Hagenbeek, A
Lokhorst, HM
机构
[1] Univ Utrecht, Dept Haematol G03647, Med Ctr, NL-3584 CX Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Immunol, NL-3584 CX Utrecht, Netherlands
[3] St Antonius Hosp, Dept Internal Med, Nieuwegein, Netherlands
关键词
cyclophosphamide; multiple myeloma; advanced myeloma;
D O I
10.1016/S0300-2977(01)00140-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Multiple myeloma is an incurable disease and after several lines of chemotherapy, patients enter a phase in which no standard treatment options are available. The poor outlook of these patients requires mild, palliative therapy with low toxicity, Previously used regimens either require frequent hospital attendance, lack efficacy or have significant toxicity. Methods: In the current study. daily low dose, oral cyclophosphamide (100 mg) and prednisone (10-20 mg; CP) were administered to patients with advanced myeloma. Forty-two patients with progressive disease after melphalan-based and VAD treatment were enrolled. Results: Objective responses were observed in 29 of 42 (69%) patients. In responding patients, median overall survival and progression-free survival were 22.2 months and 15.0 months. respectively. In non-responders, median OS was 3.5 months only. Side-effects were limited. Cytopenia was the most frequent event (8/29) prompting dose reduction. CP had to be stopped permanently in four patients (two cytopenia, two infections). Conclusion: Orally administered. low dose continuous CP is a feasible. effective and well-tolerated regimen in the management of advanced multiple myeloma. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:50 / 56
页数:7
相关论文
共 17 条
  • [1] INTERMITTENT HIGH-DOSE MELPHALAN PREDNISONE VS CONTINUOUS LOW-DOSE MELPHALAN TREATMENT IN MULTIPLE-MYELOMA
    AHRE, A
    BJORKHOLM, M
    MELLSTEDT, H
    HOLM, G
    BRENNING, G
    ENGSTEDT, L
    GAHRTON, G
    HALLEN, J
    JOHANSSON, B
    JOHANSSON, SGO
    KARNSTROM, L
    KILLANDER, A
    LERNER, R
    LOCKNER, D
    LONNQVIST, B
    SIMONSSON, B
    STALFELT, AM
    TERNSTEDT, B
    WADMAN, B
    [J]. EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1983, 19 (04): : 499 - 506
  • [2] ALEXANIAN R, 1986, ANN INTERN MED, V105, P8, DOI 10.7326/0003-4819-105-1-8
  • [3] Whither interferon for myeloma and other hematologic malignancies?
    Alexanian, R
    Weber, D
    [J]. ANNALS OF INTERNAL MEDICINE, 1996, 124 (02) : 264 - 265
  • [4] A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma
    Attal, M
    Harousseau, JL
    Stoppa, AM
    Sotto, JJ
    Fuzibet, JG
    Rossi, JF
    Casassus, P
    Maisonneuve, H
    Facon, T
    Ifrah, N
    Payen, C
    Bataille, R
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (02) : 91 - 97
  • [5] AWWAD M, 1988, IMMUNOLOGY, V65, P87
  • [6] 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
  • [7] BERGSAGEL D, 1988, J CLIN ONCOL, V5, P757
  • [8] BERGSAGEL DE, 1972, CAN MED ASSOC J, V107, P851
  • [9] BRANDES LJ, 1982, CANCER TREAT REP, V66, P1413
  • [10] MANAGEMENT OF REFRACTORY MYELOMA - A REVIEW
    BUZAID, AC
    DURIE, BGM
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (05) : 889 - 905