Immunotherapy: A new standard in the treatment of metastatic clear cell renal cell carcinoma

被引:13
|
作者
Popovic, Maja [1 ,2 ]
Matovina-Brko, Gorana [1 ]
Jovic, Masa [1 ]
Popovic, Lazar S. [1 ,2 ]
机构
[1] Univ Novi Sad, Oncol Inst Vojvodina, Dept Med Oncol, Sremska Kamenica 21204, Serbia
[2] Univ Novi Sad, Fac Med, Novi Sad 21000, Serbia
来源
WORLD JOURNAL OF CLINICAL ONCOLOGY | 2022年 / 13卷 / 01期
关键词
Renal cell carcinoma; Immunotherapy; Checkpoint inhibitors; Biomarkers; Tumor microenvironment; Programmed cell death 1 receptor; INTERFERON-ALPHA; CABOZANTINIB C; CANCER; COMBINATION; SURVIVAL; ATEZOLIZUMAB; LYMPHOCYTES; SUNITINIB; AXITINIB;
D O I
10.5306/wjco.v13.i1.28
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Renal cell cancer (RCC) represents 2%-3% of all adulthood cancers and is the most common malignant neoplasm of the kidney (90%). In the mid-nineties of the last century, the standard of treatment for patients with metastatic RCC was cytokines. Sunititib and pazopanib were registered in 2007 and 2009, respectively, and have since been the standard first-line treatment for metastatic clear cell RCC (mccRCC). Renal cell cancer is a highly immunogenic tumor with tumor infiltrating cells, including CD8+ T lymphocytes, dendritic cells, natural killer cells (NK) and macrophages. This observation led to the design of new clinical trials in which patients were treated with immunotherapy. With the growing evidence that proangiogenic factors can have immunomodulatory effects on the host's immune system, the idea of combining angiogenic drugs with immunotherapy has emerged, and new clinical trials have been designed. In the last few years, several therapeutic options have been approved [immunotherapy and immunotherapy/tyrosine kinase inhibitors (TKI)] for the first-line treatment of mccRCC. Nivolumab/ipilimumab is approved for the treatment of patients with intermediate and poor prognoses. Several checkpoint inhibitors (pembrolizumab, nivolumab, avelumab) in combination with TKI (axitinib, lenvatinib, cabozantinib) are approved for the treatment of patients regardless of their International mRCC Database Consortium prognostic group and PD-L1 expression. There is no specific and ideal biomarker that could help in selecting the ideal patient for the appropriate first-line treatment.
引用
收藏
页码:28 / 38
页数:11
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