Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Global Product Development-Oncology, Pfizer Inc, La Jolla, CA, 92121, USA.
Nat Commun. 2022 Oct 10;13(1):5959. doi: 10.1038/s41467-022-33555-8.
Multigene assays can provide insight into key biological processes and prognostic information to guide development and selection of adjuvant cancer therapy. We report a comprehensive genomic and transcriptomic analysis of tumor samples from 171 patients at high risk for recurrent renal cell carcinoma post nephrectomy from the S-TRAC trial (NCT00375674). We identify gene expression signatures, including STRAC11 (derived from the sunitinib-treated population). The overlap in key elements captured in these gene expression signatures, which include genes representative of the tumor stroma microenvironment, regulatory T cell, and myeloid cells, suggests they are likely to be both prognostic and predictive of the anti-angiogenic effect in the adjuvant setting. These signatures also point to the identification of potential therapeutic targets for development in adjuvant renal cell carcinoma, such as MERTK and TDO2. Finally, our findings suggest that while anti-angiogenic adjuvant therapy might be important, it may not be sufficient to prevent recurrence and that other factors such as immune response and tumor environment may be of greater importance.
多基因检测可深入了解关键的生物学过程和预后信息,有助于辅助癌症治疗的发展和选择。我们报告了 S-TRAC 试验(NCT00375674)中 171 例肾细胞癌切除术后有高复发风险患者的肿瘤样本的全面基因组和转录组分析。我们鉴定了基因表达特征,包括来源于舒尼替尼治疗人群的 STRAC11。这些基因表达特征中捕获的关键元素重叠,包括肿瘤基质微环境、调节性 T 细胞和髓样细胞的代表性基因,提示它们可能具有预后和预测辅助治疗中抗血管生成作用的双重作用。这些特征还表明可以确定辅助肾细胞癌治疗的潜在治疗靶点,如 MERTK 和 TDO2。最后,我们的研究结果表明,虽然抗血管生成辅助治疗可能很重要,但可能不足以预防复发,其他因素如免疫反应和肿瘤微环境可能更为重要。