Combined cyclophosphamide, vincristine, doxorubicin, and prednisone (CHOP) improves response rates but not survival and has lower hematologic toxicity compared with combined mitoxantrone, chlorambucil, and prednisone (MCP) in follicular and mantle cell lymphomas - Results of a prospective randomized trial of the German Low-Grade Lymphoma Study Group

被引:74
作者
Nickenig, Christina
Dreyling, Martin
Hoster, Eva
Pfreundschuh, Michael
Trumper, Lorenz
Reiser, Marcel
Wandt, Hannes
Lengfelder, Eva
Unterhalt, Michael
Hiddemann, Wolfgang
机构
[1] Univ Munich, Dept Internal Med 3, Munich, Germany
[2] Univ Munich, Dept Med Informat Biometr & Epidemiol, Munich, Germany
[3] Univ Hamburg, Dept Internal Med 1, Hamburg, Germany
[4] Univ Gottingen, Dept Hematol & Oncol, D-3400 Gottingen, Germany
[5] Univ Cologne, Dept Internal Med 1, Cologne, Germany
[6] Hosp Nurnberg Nord, Dept Internal Med 5, Nurnberg, Germany
[7] Univ Mannheim, Dept Internal Med 3, Mannheim, Germany
关键词
indolent lymphoma; chemotherapy; randomized trial; first-line therapy;
D O I
10.1002/cncr.22093
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. in patients with advanced-stage follicullar lymphoma (FL) and mantle cell lymphoma (MCL), conventional chemotherapy remains a noncurative approach, and no major improvement in overall survival has been achieved in recent decades. METHODS. The German Low-Grade Lymphoma Study Group performed a randomized trial comparing combined cyclophosphamide, vincristine, doxorubicin, and prednisone (CHOP) chemotherapy with combined mitoxantrone, chlorambucil, and prednisone (MCP) chemotherapy as first-line therapy for patients with advanced-stage FL or MCL. RESULTS. Three hundred sixty-three patients with advanced-stage FL (n = 277 patients) or MCL (n 86 patients) entered the trial and were evaluable fully. CHOP resulted in a significantly higher overall response rate in patients with FL (91% vs. 82%; P = .026) and a similar tendency in patients with MCL (87% vs. 73%; P = .080). However, no significant differences were observed in the time to treatment failure or in overall survival. CHOP produced significantly more nonhematologic toxicities, whereas MCP was associated with more severe hematologic side effects. The proportion of patients who successfully underwent peripheral blood stem cell collection was significantly lower after MCP (44% vs. 93% after CHOP; P =.0003). CONCLUSIONS. Taking into account that, currently, chemotherapy regularly is combined with rituximab as first-line therapy for FL and MCL, the data from this study may have an impact on the type of chemotherapy to be applied in such combinations. Particularly in younger, high-risk patients who are candidates for autologous stem cell transplantation, CHOP should be preferred over MCP.
引用
收藏
页码:1014 / 1022
页数:9
相关论文
共 28 条
  • [11] World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: Report of the Clinical Advisory Committee Meeting - Airlie House, Virginia, November 1997
    Harris, NL
    Jaffe, ES
    Diebold, J
    Flandrin, G
    Muller-Hermelink, HK
    Vardiman, J
    Lister, TA
    Bloomfield, CD
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (12) : 3835 - 3849
  • [12] Randomized phase III study for the treatment of advanced indolent non-Hodgkin's lymphomas (NHL) and mantle cell lymphoma:: chemotherapy versus chemotherapy plus rituximab
    Herold, M
    Dölken, G
    Fiedler, F
    Franke, A
    Freund, M
    Helbig, W
    Pasold, R
    [J]. ANNALS OF HEMATOLOGY, 2003, 82 (02) : 77 - 79
  • [13] HIDDEMANN W, 1990, SEMIN ONCOL, V17, P20
  • [14] Frontline therapy with rituximab added to the combination of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) significantly improves the outcome for patients with advanced-stage follicular lymphoma compared with therapy with CHOP alone:: results of a prospective randomized study of the German Low-Grade Lymphoma Study Group
    Hiddemann, W
    Kneba, M
    Dreyling, M
    Schmitz, N
    Lengfelder, E
    Schmits, R
    Reiser, M
    Metzner, B
    Harder, H
    Hegewisch-Becker, S
    Fischer, T
    Kropff, M
    Reis, HE
    Freund, M
    Wörmann, B
    Fuchs, R
    Planker, M
    Schimke, J
    Eimermacher, H
    Trümper, L
    Aldaoud, A
    Parwaresch, R
    Unterhalt, M
    [J]. BLOOD, 2005, 106 (12) : 3725 - 3732
  • [15] Rituximab (anti-CD20 monoclonal antibody) as consolidation of first-line CHOP chemotherapy in patients with follicular lymphoma:: a phase II study
    Jäeger, G
    Neumeister, P
    Brezinschek, R
    Höfler, G
    Quehenberger, F
    Linkesch, W
    Sill, H
    [J]. EUROPEAN JOURNAL OF HAEMATOLOGY, 2002, 69 (01) : 21 - 26
  • [16] LANDYS KE, 1988, INVEST NEW DRUG, V6, P105
  • [17] Moderate increase of secondary hematologic malignancies after myeloablative radiochemotherapy and autologous stem-cell transplantation in patients with indolent lymphoma: Results of a prospective randomized trial of the German Low Grade Lymphoma Study Group
    Lenz, G
    Dreyling, M
    Schiegnitz, E
    Haferlach, T
    Hasford, J
    Unterhalt, M
    Hiddemann, W
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (24) : 4926 - 4933
  • [18] Myeloablative radiochemotherapy followed by autologous stem cell transplantation in first remission prolongs progression-free survival in follicular lymphoma: results of a prospective, randomized trial of the German Low-Grade Lymphoma Study Group
    Lenz, G
    Dreyling, M
    Schiegnitz, E
    Forstpointner, R
    Wandt, H
    Freund, M
    Hess, G
    Truemper, L
    Diehl, V
    Kropff, M
    Kneba, M
    Schmitz, N
    Metzner, B
    Pfirrmann, M
    Unterhalt, M
    Hiddemann, W
    [J]. BLOOD, 2004, 104 (09) : 2667 - 2674
  • [19] COMPARISON OF COMBINED AND SINGLE-AGENT CHEMOTHERAPY IN NON-HODGKINS LYMPHOMA OF FAVORABLE HISTOLOGICAL TYPE
    LISTER, TA
    CULLEN, MH
    BEARD, MEJ
    BREARLEY, RL
    WHITEHOUSE, JMA
    WRIGLEY, PFM
    STANSFELD, AG
    SUTCLIFFE, SBJ
    MALPAS, JS
    CROWTHER, D
    [J]. BRITISH MEDICAL JOURNAL, 1978, 1 (6112) : 533 - 537
  • [20] CVP chemotherapy plus rituximab compared with CVP as first-line treatment for advanced follicular lymphoma
    Marcus, R
    Imrie, K
    Belch, A
    Cunningham, D
    Flores, E
    Catalano, J
    Solal-Celigny, P
    Offner, F
    Walewski, J
    Raposo, J
    Jack, A
    Smith, P
    [J]. BLOOD, 2005, 105 (04) : 1417 - 1423