Medical Oncology Unit, University Hospital of Parma, Parma, Italy.
Department of Medical Oncology, IRCCS San Martino IST, Genova, Italy.
Expert Rev Mol Diagn. 2020 Feb;20(2):169-185. doi: 10.1080/14737159.2019.1680286. Epub 2019 Oct 24.
: In recent years, the treatment landscape of metastatic renal cell carcinoma (mRCC) has been improved using immune-checkpoint inhibitors (ICI). Nevertheless, the number of patients experiencing clinical benefit from immunotherapy is still limited, while others obtain more benefit from tyrosine kinase inhibitors (TKI). The identification of prognostic and predictive factors would be crucial to better select patients most likely to benefit from immunotherapy among the other potentially available therapeutic options.: This systematic review summarizes the current knowledge (2010-2019) on molecular prognostic and predictive biomarkers, assessed in peripheral blood and/or from tumor tissue, in mRCC patients treated with ICI.: Among all the biomarkers analyzed, PD-L1 expression on tumor tissue is the most studied. It has an unfavorable prognostic role for patients treated with TKI, which seems to be overcome by ICI-based combinations. Nevertheless, no clear predictive role of immunotherapy efficacy has been observed for PD-L1 in mRCC. Emerging evidence regarding pro-angiogenic or pro-immunogenic genomic and transcriptomic signatures suggests a potential predictive role in patients treated with ICI-based combinations. The rationale for TKI-ICI combinations is based on tumor microenvironment and genomic background, which represent the target of these two main therapeutic options for mRCC.
近年来,免疫检查点抑制剂(ICI)的应用改善了转移性肾细胞癌(mRCC)的治疗前景。然而,从免疫治疗中获得临床获益的患者数量仍然有限,而其他患者从酪氨酸激酶抑制剂(TKI)中获益更多。确定预后和预测因素对于在其他潜在治疗选择中更好地选择最有可能从免疫治疗中获益的患者至关重要。
本系统综述总结了 2010 年至 2019 年期间关于在接受 ICI 治疗的 mRCC 患者的外周血和/或肿瘤组织中评估的分子预后和预测生物标志物的现有知识。
在所有分析的生物标志物中,肿瘤组织上 PD-L1 的表达是研究最多的。它对接受 TKI 治疗的患者具有不利的预后作用,而这种作用似乎可以通过基于 ICI 的联合治疗来克服。然而,在 mRCC 中,PD-L1 对免疫治疗疗效没有明显的预测作用。关于促血管生成或促免疫原性基因组和转录组特征的新证据表明,在接受基于 ICI 的联合治疗的患者中有潜在的预测作用。TKI-ICI 联合治疗的原理基于肿瘤微环境和基因组背景,这是 mRCC 这两种主要治疗选择的目标。