Pilskog Martin, Nilsen Gry Hilde, Beisland Christian, Straume Oddbjørn
Centre for Cancer Biomarkers, University of Bergen, Norway; Department of Oncology, Haukeland University Hospital, Bergen, Norway.
Department of Clinical Medicine, University of Bergen, Norway.
Cancer Treat Res Commun. 2019;19:100127. doi: 10.1016/j.ctarc.2019.100127. Epub 2019 Mar 14.
Clear cell renal cell carcinoma (ccRCC) is the most common type among renal cell carcinomas, and anti-angiogenic treatment is currently first line therapy in metastatic ccRCC (mccRCC). Response rates and duration of response show considerable variation, and adverse events have major influence on patient's quality of life. The need for predictive biomarkers to select those patients most likely to respond to receptor tyrosine kinase inhibitors (rTKI) upfront is urgent. We investigated the predictive value of plasma interleukin-6 (pIL6), interleukin-6 receptor α (pIL6Rα) and interleukin 6 signal transducer (pIL6ST) in mccRCC patients treated with sunitinib.
Forty-six patients with metastatic or non-resectable ccRCC treated with sunitinib were included. Full blood samples were collected at baseline before start of sunitinib and after every second cycle of treatment during the study time. pIL6, pIL6R and pIL6ST at baseline and week 12 samples were analysed by ELISA. The predictive potential of the candidate markers was assessed by correlation with response rates (RECIST). In addition, progression free survival (PFS) and overall survival (OS) were analysed.
Low pIL6 at baseline was significantly associated with improved response to sunitinib (Fisher's exact test, p < 0.01). Furthermore, low pIL6 at baseline was significantly associated with improved PFS (log rank, p = 0.04). In addition, patients with a decrease in concentration of pIL6R between baseline and week 12 showed significantly improved PFS (log rank, p = 0.04) and patients with high pIL6ST at baseline showed significantly improved OS (log rank, p = 0.03).
Low pIL6 at baseline in mccRCC patients treated with sunitinib predicts improved treatment response, and might represent a candidate predictive marker.
透明细胞肾细胞癌(ccRCC)是肾细胞癌中最常见的类型,抗血管生成治疗目前是转移性ccRCC(mccRCC)的一线治疗方法。缓解率和缓解持续时间存在相当大的差异,不良事件对患者的生活质量有重大影响。迫切需要预测性生物标志物来预先选择那些最有可能对受体酪氨酸激酶抑制剂(rTKI)产生反应的患者。我们研究了血浆白细胞介素-6(pIL6)、白细胞介素-6受体α(pIL6Rα)和白细胞介素6信号转导子(pIL6ST)在接受舒尼替尼治疗的mccRCC患者中的预测价值。
纳入46例接受舒尼替尼治疗的转移性或不可切除ccRCC患者。在舒尼替尼开始治疗前的基线期以及研究期间每两个治疗周期后采集全血样本。通过酶联免疫吸附测定(ELISA)分析基线期和第12周样本中的pIL6、pIL6R和pIL6ST。通过与缓解率(RECIST)的相关性评估候选标志物的预测潜力。此外,还分析了无进展生存期(PFS)和总生存期(OS)。
基线期低水平的pIL6与舒尼替尼治疗反应的改善显著相关(Fisher精确检验,p < 0.01)。此外,基线期低水平的pIL6与PFS的改善显著相关(对数秩检验,p = 0.04)。此外,基线期至第12周pIL6R浓度降低的患者PFS显著改善(对数秩检验,p = 0.04),基线期高水平pIL6ST的患者OS显著改善(对数秩检验,p = 0.03)。
接受舒尼替尼治疗的mccRCC患者基线期低水平的pIL6预示治疗反应改善,可能是一种候选预测标志物。