Risk-adapted (immuno)therapy for renal cell carcinoma

被引:3
|
作者
Gruenwald, V. [1 ]
机构
[1] Univ Klinikum Essen, Interdisziplinare Uroonkol, Westdeutschen Tumorzentrum, Hufelandstr 55, D-45147 Essen, Germany
来源
UROLOGE | 2018年 / 57卷 / 11期
关键词
Medical treatment; Targeted therapy; Cabozantinib; Tivozanib; Tyrosine kinase inhibitor; TARGETED THERAPY; INTERFERON-ALPHA; SUNITINIB; SURVIVAL; CABOZANTINIB; VALIDATION; EVEROLIMUS; SORAFENIB; MODEL;
D O I
10.1007/s00120-018-0791-3
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
The introduction of immunotherapy into the therapeutic algorithm of metastatic renal cell carcinoma (mRCC) represents the most recent expansion of the therapy landscape. This provides anew therapeutic axis in addition to targeted therapies. At the same time, the development of new tyrosine kinase inhibitors (TKIs) has led to an improvement in the effectiveness of targeted therapies. Cabozantinib and tivozanib are two new first-line options that redefine the existing therapy algorithm. The importance of the checkpoint blockade in the first line is clinically undisputed; however, approval of the immune combination ipilimumab+nivolumab has not yet been granted. An important task now is to offer risk-adapted therapy in order to optimally balance efficacy and risks of systemic therapy, thereby ensuring the best possible individual therapy.
引用
收藏
页码:1326 / 1333
页数:8
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