Novel approaches in the therapy of metastatic renal cell carcinoma

被引:196
作者
Lam, JS
Leppert, JT
Belldegrun, AS
Figlin, RA
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Urol, Los Angeles, CA 90095 USA
关键词
anti-angiogenesis; cancer; carbonic anhydrase IX; kidney; metastases; small molecule inhibitors; therapy;
D O I
10.1007/s00345-004-0466-0
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Renal cell carcinoma (RCC) is the most lethal of the common urologic malignancies, with approximately 40% of patients eventually dying of cancer progression. Approximately one third of patients present with metastatic disease, and up to 40% treated for localized disease have a recurrence. Recent advances in the understanding of the pathogenesis, behavior, and molecular biology of RCC have paved the way for developments that may enhance early diagnosis, better predict tumor prognosis, and improve survival for RCC patients. The recent discovery of molecular tumor markers is expected to revolutionize the staging of RCC in the future and lead to the development of new therapies based on molecular targeting. Cytokine-based immunotherapy can be considered standard therapy in the treatment of metastatic RCC today. However, new therapies such as tumor vaccines, anti-angiogenesis agents, and small molecule inhibitors are being developed to improve efficacy and treat those patients who are unable to tolerate or are resistant to systemic immunotherapy. The aim of this review is to provide an update on current therapeutic approaches and targeted molecular therapy for metastatic RCC.
引用
收藏
页码:202 / 212
页数:11
相关论文
共 103 条
  • [51] Loncaster JA, 2001, CANCER RES, V61, P6394
  • [52] FIH-1:: a novel protein that interacts with HIF-1α and VHL to mediate repression of HIF-1 transcriptional activity
    Mahon, PC
    Hirota, K
    Semenza, GL
    [J]. GENES & DEVELOPMENT, 2001, 15 (20) : 2675 - 2686
  • [53] Inhibitory PAS domain protein (IPAS) is a hypoxia-inducible splicing variant of the hypoxia-inducible factor-3α locus
    Makino, Y
    Kanopka, A
    Wilson, WJ
    Tanaka, H
    Poellinger, L
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (36) : 32405 - 32408
  • [54] Marshall John L, 2002, J Exp Ther Oncol, V2, P325, DOI 10.1046/j.1359-4117.2002.01039.x
  • [55] The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis
    Maxwell, PH
    Wiesener, MS
    Chang, GW
    Clifford, SC
    Vaux, EC
    Cockman, ME
    Wykoff, CC
    Pugh, CW
    Maher, ER
    Ratcliffe, PJ
    [J]. NATURE, 1999, 399 (6733) : 271 - 275
  • [56] Radical nephrectomy plus interferon-alfa-based immunotherapy compared with interferon alfa alone in metastatic renal-cell carcinoma: a randomised trial
    Mickisch, GHJ
    Garin, A
    van Poppel, H
    de Prijck, L
    Sylvester, R
    [J]. LANCET, 2001, 358 (9286) : 966 - 970
  • [57] Systemic therapy for renal cell carcinoma
    Motzer, RJ
    Russo, P
    [J]. JOURNAL OF UROLOGY, 2000, 163 (02) : 408 - 417
  • [58] Phase II trial of antiepidermal growth factor receptor antibody C225 in patients with advanced renal cell carcinoma
    Motzer, RJ
    Amato, R
    Todd, M
    Hwu, WJP
    Cohen, R
    Baselga, J
    Muss, H
    Cooper, M
    Yu, R
    Ginsberg, MS
    Needle, M
    [J]. INVESTIGATIONAL NEW DRUGS, 2003, 21 (01) : 99 - 101
  • [59] Treatment outcome and survival associated with metastatic renal cell carcinoma of non-clear-cell histology
    Motzer, RJ
    Bacik, J
    Mariani, T
    Russo, P
    Mazumdar, M
    Reuter, V
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (09) : 2376 - 2381
  • [60] Phase II trial of thalidomide for patients with advanced renal cell carcinoma
    Motzer, RJ
    Berg, W
    Ginsberg, M
    Russo, P
    Vuky, J
    Yu, R
    Bacik, J
    Mazumdar, M
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (01) : 302 - 306