Recent progress in target therapy in colorectal cancer

被引:0
作者
Pasetto, Lara Maria
Bortolami, Alberto
Falci, Cristina
Sinigaglia, Giulietta
Monfardini, Silvio
机构
[1] Ist Oncol Veneto, I-35128 Padua, Italy
[2] Ctr Riferimento Oncol, UO Farmacol Sperimentale & Clin, I-33081 Aviano, Italy
关键词
bevacizumab; cetuximab; colorectal cancer; review;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Monoclonal antibodies are a new class of agents targeting at specific receptors on cancer cells. In addition to having direct cellular effects, antibodies can carry substances, such as radioactive isotopes, toxins and antineoplastic agents, to the targeted cells. Two of them, cetuximab (Erbitux (R)) and bevacizumab (Avastin (R)), seem to have acquired a significant role in the management of patients with radically resected and advanced colorectal carcinoma. Cetuximab plus irinotecan has been approved as second-line therapy in irinotecan-resistant colorectal cancer patients; bevacizumab plus 5FU/LV has resulted in higher response and longer survival than 5FU/LV alone in first line metastatic colorectal cancer; its combination with oxaliplatin has recently doubled results. The superior therapeutic efficacy of these molecular targeting agents over traditional chemotherapy has been shown by the survival benefit achieved by patients with advanced or recurrent cancers. Although the precise molecular mechanism by which these agents produce or enhance an antitumour effect, alone or in combination with anticancer drugs, is unknown, the specific inhibition of target genes critically involved in tumour progression and metastasis is clear. Further studies to determine which patient groups and anticancer drugs are more appropriate for combination therapy with these agents are needed. All the most important data obtained through recent studies are discussed, emphasizing their mechanisms of action, safety, profiles and clinical applications.
引用
收藏
页码:3973 / 3981
页数:9
相关论文
共 57 条
  • [1] ABUBAKR Y, 2006, P AM SOC CLIN ONCOL, V25
  • [2] Maximizing the potential of bevacizumab in cancer treatment
    Bergsland, E
    Dickler, MN
    [J]. ONCOLOGIST, 2004, 9 : 36 - 42
  • [3] Boige V, 2005, B CANCER, V92, pS29
  • [4] Buecher B, 2005, ANTICANCER RES, V25, P225
  • [5] CHAWLA A, 2005, P AM SOC CLIN ONCOL, V24
  • [6] Phase II multicenter trial of bevacizumab plus fluorouracil and leucovorin in patients with advanced refractory colorectal cancer: An NCI Treatment Referral Center trial TRC-0301
    Chen, Helen X.
    Mooney, Margaret
    Boron, Matthew
    Vena, Don
    Mosby, Kimberly
    Grochow, Louise
    Jaffe, Carl
    Rubinstein, Lawrence
    Zwiebel, James
    Kaplan, Richard S.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (21) : 3354 - 3360
  • [7] Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer
    Cunningham, D
    Humblet, Y
    Siena, S
    Khayat, D
    Bleiberg, H
    Santoro, A
    Bets, D
    Mueser, M
    Harstrick, A
    Verslype, C
    Chau, I
    Van Cutsem, E
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (04) : 337 - 345
  • [8] Targeting the epidermal growth factor receptor in the treatment of colorectal cancer - State of the art
    Diasio, Robert B.
    Fourie, Jeanne
    [J]. DRUGS, 2006, 66 (11) : 1441 - 1463
  • [9] Targeting the epidermal growth factor receptor
    El-Rayes, BF
    LoRusso, PM
    [J]. BRITISH JOURNAL OF CANCER, 2004, 91 (03) : 418 - 424
  • [10] Multi-institutional randomized phase II trial of gefitinib for previously treated patients with advanced non-small-cell lung cancer
    Fukuoka, M
    Yano, S
    Giaccone, G
    Tamura, T
    Nakagawa, K
    Douillard, JY
    Nishiwaki, Y
    Vansteenkiste, J
    Kudoh, S
    Rischin, D
    Eek, R
    Horai, T
    Noda, K
    Takata, I
    Smit, E
    Averbuch, S
    Macleod, A
    Feyereislova, A
    Dong, RP
    Baselga, J
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (12) : 2237 - 2246