Kidney Cancer Section, Memorial Sloan Kettering Cancer Center, New York, New York, USA
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
J Immunother Cancer. 2022 Mar;10(3). doi: 10.1136/jitc-2021-004316.
The phase 3 CheckMate 214 trial demonstrated higher response rates and improved overall survival with nivolumab plus ipilimumab versus sunitinib in first-line therapy for advanced clear-cell renal cell carcinoma (RCC). An unmet need exists to identify patients with RCC who are most likely to benefit from treatment with nivolumab plus ipilimumab.
In exploratory analyses, pretreatment levels of programmed death ligand 1 were assessed by immunohistochemistry. Genomic and transcriptomic biomarkers (including tumor mutational burden and gene expression signatures) were also investigated.
Biomarkers previously associated with benefit from immune checkpoint inhibitor-containing regimens in RCC were not predictive for survival in patients with RCC treated with nivolumab plus ipilimumab. Analysis of gene expression identified an association between an inflammatory response and progression-free survival with nivolumab plus ipilimumab.
The exploratory analyses reveal relationships between molecular biomarkers and provide supportive data on how the inflammation status of the tumor microenvironment may be important for identifying predictive biomarkers of response and survival with combination immunotherapy in patients with RCC. Further validation may help to provide biomarker-driven precision treatment for patients with RCC.
CheckMate 214 三期临床试验表明,纳武利尤单抗联合伊匹单抗一线治疗晚期透明细胞肾细胞癌(RCC)的疗效优于舒尼替尼,可提高缓解率和总生存率。目前仍需要确定哪些 RCC 患者最有可能从纳武利尤单抗联合伊匹单抗治疗中获益。
采用免疫组织化学法检测程序性死亡配体 1 的预处理水平。还研究了基因组和转录组生物标志物(包括肿瘤突变负担和基因表达特征)。
先前与 RCC 免疫检查点抑制剂治疗获益相关的生物标志物不能预测接受纳武利尤单抗联合伊匹单抗治疗的 RCC 患者的生存情况。基因表达分析表明,纳武利尤单抗联合伊匹单抗治疗与无进展生存期之间存在炎症反应的关联。
探索性分析揭示了分子生物标志物之间的关系,并提供了关于肿瘤微环境炎症状态如何有助于确定 RCC 患者联合免疫治疗反应和生存预测生物标志物的支持性数据。进一步的验证可能有助于为 RCC 患者提供基于生物标志物的精准治疗。