Renal cell carcinoma: novel treatments for advanced disease

被引:6
作者
Huland, E [1 ]
Heinzer, H [1 ]
机构
[1] Univ Hamburg, Hosp Eppendorf, Dept Urol, D-20246 Hamburg, Germany
关键词
cytokines; interleukin 2 and interferon; cytoreductive surgery and radiation; aerosol interleukin 2; antibody based immunotherapy; advanced renal cancer;
D O I
10.1097/00042307-200311000-00005
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
Purpose of review IL-2 or IFN-alpha induce remissions and prolong life in patients carefully selected for a possibly toxic treatment. However, there is a need for better-tolerated and more effective therapies, especially in patients with co-morbidities and those resistant to systemic immunotherapy. Recent achievements in the treatment of advanced renal cell carcinoma highlight potentially significant improvements. Recent findings Cytoreductive surgery or radiation of metastases seems beneficial in well-selected patients, especially as immunotherapy is available. Immune cells within the tumour correlate with response and survival, indicating the importance of local immune modulation. Such modulation has allowed the introduction of well-tolerated treatments such as the inhalation of IL-2 to control lung metastases, which results in a significant survival benefit for high-risk patients, as suggested by a recent outcome study in 200 patients. Antibody-based tumour targeting against cG250, specifically expressed on renal cell carcinoma, seems to stabilize progressive metastatic disease and does not induce toxicity. Vaccination strategies are also well tolerated, but have not yet shown convincing results in advanced disease. Other approaches have not fulfilled expectations. Thalidomide has significant neurotoxicity and its efficacy was not confirmed in recent studies. Stem cell transplantation has significant toxicity, and cannot yet be recommended, but may have future potential. Summary Cytokine-based immunotherapy can now be considered standard in the treatment of metastatic renal cell carcinoma. There is good evidence that additional local procedures such as surgery, radiation or the inhalation of IL-2 improve response and survival in metastatic disease with moderate toxicity, resulting in a significant improvement for patients suitable for these approaches.
引用
收藏
页码:451 / 456
页数:6
相关论文
共 43 条
[1]  
ASSIKIS VJ, 2002, PROSPECTIVE STUDY SA
[2]   Thirteen-year, long-term efficacy of interferon 2α and interleukin 2-based home therapy in patients with advanced renal cell carcinoma [J].
Atzpodien, J ;
Hoffmann, R ;
Franzke, M ;
Stief, C ;
Wandert, T ;
Reitz, M .
CANCER, 2002, 95 (05) :1045-1050
[3]   Dendritic cell immunotherapy for patients with metastatic renal cell carcinoma: University of Tokyo experience [J].
Azuma, T ;
Horie, S ;
Tomita, K ;
Takahashi, T ;
Tanaka, Y ;
Kashiwase, K ;
Nieda, M ;
Takeuchi, T ;
Ohta, N ;
Shibata, Y ;
Hirai, H ;
Kitamura, T .
INTERNATIONAL JOURNAL OF UROLOGY, 2002, 9 (06) :340-346
[4]   Neovastat (Æ-941) in refractory renal cell carcinoma patients:: report of a phase II trial with two dose levels [J].
Batist, G ;
Patenaude, F ;
Champagne, P ;
Croteau, D ;
Levinton, C ;
Hariton, C ;
Escudier, B ;
Dupont, E .
ANNALS OF ONCOLOGY, 2002, 13 (08) :1259-1263
[5]  
BOEHM M, 2002, FOLIA BIOL, V49, P63
[6]   Nonmyeloablative conditioning followed by hematopoietic cell allografting and donor lymphocyte infusions for patients with metastatic renal and breast cancer [J].
Bregni, M ;
Dodero, A ;
Peccatori, J ;
Pescarollo, A ;
Bernardi, M ;
Sassi, I ;
Voena, C ;
Zaniboni, A ;
Bordignon, C ;
Corradini, P .
BLOOD, 2002, 99 (11) :4234-4236
[7]  
BRINKMAN OA, C GERM SOC UR 2002
[8]   Pegylated interferon alfa-2b treatment for patients with solid tumors: A phase I/II study [J].
Bukowski, R ;
Ernstoff, MS ;
Gore, ME ;
Nemunaitis, JJ ;
Amato, R ;
Gupta, SK ;
Tendler, CL .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (18) :3841-3849
[9]   Phase II trial of autologous tumor vaccination, anti-CD3-activated vaccine-primed lymphocytes, and interleukin-2 in stage IV renal cell cancer [J].
Chang, AE ;
Li, Q ;
Jiang, GH ;
Sayre, DM ;
Braun, TM ;
Redman, BG .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (05) :884-890
[10]  
COTRAN RS, 1988, J IMMUNOL, V140, P1883