转移性透明细胞肾细胞癌一线治疗的当前和新兴疗法

M. Serzan, M. Atkins
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引用次数: 5

摘要

随着对疾病生物学知识的提高,晚期透明细胞肾细胞癌(ccRCC)的治疗前景正在迅速发展,从而引入了各种抗血管生成药物和免疫疗法。在这篇综述中,我们讨论了晚期ccRCC患者的历史、当前和新兴的一线治疗方案。其中包括单剂血管内皮生长因子受体酪氨酸激酶抑制剂(TKIs)的数据:舒尼替尼、帕唑帕尼和卡博扎替尼,以及最近报道的乐伐替尼和依维莫司联合用药(mTOR抑制剂)的结果。我们还讨论了nivolumab抗程序性细胞死亡(PD-1)/ipilimumab(抗细胞毒性T淋巴细胞相关抗原4)组合的结果,以及nivoluma和pembrolizumab(抗PD-1)单药治疗的新一线数据。最后,我们回顾了支持TKI和抗PD-1或抗PD配体1(PD-L1)组合(例如,阿西替尼/pembrolizumab、阿西替尼/阿维鲁单抗和卡博扎替尼/尼沃单抗)最近批准的数据,以及乐伐替尼(多激酶抑制剂)和pembrolizomab的初步结果。由于有许多单独和联合治疗选择,而且缺乏面对面的比较,治疗选择将取决于治疗目标(终点)以及与所需治疗终点相关的临床和基于肿瘤的预测生物标志物的识别和验证。
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Current and emerging therapies for first line treatment of metastatic clear cell renal cell carcinoma
The therapeutic landscape for advanced clear cell renal cell carcinoma (ccRCC) is rapidly evolving with improved knowledge of the biology of disease leading to the incorporation of a variety of antiangiogenic agents and immunotherapies. In this review, we discuss historical, current, and emerging first line treatment options for patients with advanced ccRCC. These include data with single agent vascular endothelial growth factor receptor tyrosine kinase inhibitors (TKIs): sunitinib, pazopanib and cabozantinib as well as the recently reported results for the combination of lenvatinib and everolimus (mTOR inhibitor). We also discuss results of the nivolumab anti-programmed cell death (PD-1)/ipilimumab (anti-cytotoxic T lymphocyte-associated antigen 4) combination as well as emerging front-line data with nivolumab and pembrolizumab (anti-PD-1) monotherapy. Finally, we review data supporting recent approvals of TKI and anti-PD-1 or anti-PD-Ligand 1 (PD-L1) combinations (e.g., axitinib/pembrolizumab, axitinib/avelumab and cabozantinib/nivolumab) and initial outcomes of lenvatinib (multi-kinase inhibitor) and pembrolizumab. With many individual and combination treatment options and the lack of head-to-head comparisons, treatment selection will depend on the goals of therapy (endpoints) and the identification and validation of clinical and tumor-based predictive biomarkers that are linked to the desired treatment endpoints.
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CiteScore
3.20
自引率
5.30%
发文量
460
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