Efficacy, tolerability and management of raltitrexed (Tomudex™) monotherapy in patients with advanced colorectal cancer:: a review of phase II/III trials

被引:60
作者
Cunningham, D
Zalcberg, J
Maroun, J
James, R
Clarke, S
Maughan, TS
Vincent, M
Schulz, J
Barón, MG
Facchini, T
机构
[1] Royal Marsden Hosp, GI Unit, Sutton, Surrey, England
[2] Peter MacCallum Canc Inst, Div Haematol & Med Oncol, Melbourne, Vic 3000, Australia
[3] Ottawa Reg Canc Ctr, Dept Med Oncol, Ottawa, ON K1Y 4K7, Canada
[4] Maidstone Dist Gen Hosp, Kent Canc Ctr, Maidstone, Kent, England
[5] Royal Prince Alfred Hosp, Dept Med Oncol, Sydney Canc Ctr, Camperdown, NSW 2050, Australia
[6] Velindre Hosp, Dept Clin Oncol, Cardiff, S Glam, Wales
[7] London Reg Canc Ctr, London, ON, Canada
[8] Hosp La Paz, Med Oncol Serv, Madrid, Spain
[9] Polyclin Courlancy, Reims, France
关键词
raltitrexed; tolerability; creatinine clearance; toxicity;
D O I
10.1016/S0959-8049(01)00413-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Raltitrexed (Tomudex(TM)), a thymidylate synthase inhibitor, is an alternative to 5-fluorouracil (5-FU) leucovorin (LV) for the first-line treatment of advanced colorectal cancer. Following the completion or four phase III studies with raltitrexed at the recommended dose of 3.0 mg/m(2), it is opportune to review the efficacy and tolerability data of raltitrexed and Suggest guidelines for appropriate patient management. Data are analysed from four phase III and five phase II studies including over 1300 patients with advanced colorectal cancer, some of whom were elderly or received higher doses of raltitrexed. Median survival with raltitrexed was comparable to that of bolus or infusional 5-FU/LV in three of the four randomised studies' and objective response rates in the four trials were similar for the two agents. Response rates were at least comparable in elderly patients in phase II studies. For the majority of patients, treatment with raltitrexed was well tolerated even at doses higher than that recommended or in the elderly. As with other cytotoxic agents, serious and potentially life-threatening side-effects can occur, nevertheless, adherence to simple patient guidelines should minimise the incidence of serious side-effects with raltitrexed these include the assessment of renal function before each and every treatment, dosage adjustment ill the presence of renal impairment and close monitoring with prompt treatment of toxicities, particularly diarrhoea and neutropenia. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:478 / 486
页数:9
相关论文
共 23 条
  • [1] Metabolism, excretion and pharmacokinetics of a single dose of [14C]-raltitrexed in cancer patients
    Beale, P
    Judson, I
    Hanwell, J
    Berry, C
    Aherne, W
    Hickish, T
    Martin, P
    Walker, M
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1998, 42 (01) : 71 - 76
  • [2] Phase I trial of ZDI694, a new folate-based thymidylate synthase inhibitor, in patients with solid tumors
    Clarke, SJ
    Hanwell, J
    deBeer, M
    Planting, A
    VerweiJ, J
    Walker, M
    Smith, R
    Jackman, AL
    Hughes, LR
    Harrap, KR
    Kennealey, GT
    Judson, IR
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (05) : 1495 - 1503
  • [3] Open, randomized, multicenter trial of raltitrexed versus fluorouracil plus high-dose leucovorin in patients with advanced colorectal cancer
    Cocconi, G
    Cunningham, D
    Van Cutsem, E
    Francois, E
    Gustavsson, B
    van Hazel, G
    Kerr, D
    Possinger, K
    Hietschold, SM
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (09) : 2943 - 2952
  • [4] PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE
    COCKCROFT, DW
    GAULT, MH
    [J]. NEPHRON, 1976, 16 (01) : 31 - 41
  • [5] Final results of a randomised trial comparing 'Tomudex'(R) (raltitrexed) with 5-fluorouracil plus leucovorin in advanced colorectal cancer
    Cunningham, D
    Zalcberg, JR
    Rath, U
    Oliver, I
    vanCutsem, E
    Svensson, C
    Seitz, JF
    Harper, P
    Kerr, D
    PerezManga, G
    [J]. ANNALS OF ONCOLOGY, 1996, 7 (09) : 961 - 965
  • [6] CLINICAL-PHARMACOLOGY OF 5-FLUOROURACIL
    DIASIO, RB
    HARRIS, BE
    [J]. CLINICAL PHARMACOKINETICS, 1989, 16 (04) : 215 - 237
  • [7] FACCHINI T, 2000, P AN M AM SOC CLIN, V19, pA298
  • [8] Farrugia DC, 2000, CLIN CANCER RES, V6, P3646
  • [9] Grem JL, 1999, CLIN CANCER RES, V5, P2381
  • [10] Horikoshi N, 1998, Gan To Kagaku Ryoho, V25, P2075