Division of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.
Urol Oncol. 2013 Jan;31(1):42-50. doi: 10.1016/j.urolonc.2010.09.008. Epub 2011 Mar 10.
To investigate the expression levels of multiple molecular markers in radical nephrectomy specimens from patients with metastatic renal cell carcinoma (RCC) treated with sorafenib in order to identify factors predicting susceptibility to this agent.
This study included 45 consecutive patients undergoing radical nephrectomy for clear cell RCC who were diagnosed as having metastatic diseases refractory to cytokine therapy and subsequently treated with sorafenib. Expression levels of 19 molecular markers involved in the regulation of apoptosis, cell cycle, signal transduction, and angiogenesis in primary RCC specimens were measured by immunohistochemical staining.
There was no molecular marker having significant impact on the prediction of response to sorafenib. However, progression-free survival (PFS) was significantly associated with the expression levels of Bcl-xL and platelet-derived growth factor receptor (PDGFR)-α in addition to the presence of bone metastasis and C-reactive protein level on univariate analysis. Of these significant factors, PDGFR-α expression and the presence of bone metastasis appeared to be independently related to PFS by multivariate analysis. Furthermore, there were significant differences in PFS according to positive numbers of these 2 independent risk factors; that is, disease progression occurred in 2 of 7 patients who were negative for risk factor, 19 of 34 positive for a single risk factor, and 6 of 6 positive for both risk factors.
Collectively, these findings suggest that it would be useful to consider expression levels of potential molecular markers, particularly PDGFR-α, as well as clinical parameters to select metastatic RCC patients likely to benefit from treatment with sorafenib.
研究索拉非尼治疗转移性肾细胞癌(RCC)患者根治性肾切除术后标本中多个分子标志物的表达水平,以确定预测该药物敏感性的因素。
本研究纳入 45 例因对细胞因子治疗耐药而接受根治性肾切除术治疗的透明细胞 RCC 患者,这些患者被诊断为转移性疾病,并随后接受索拉非尼治疗。通过免疫组织化学染色,检测原发性 RCC 标本中涉及凋亡、细胞周期、信号转导和血管生成调节的 19 个分子标志物的表达水平。
没有分子标志物对索拉非尼的反应预测有显著影响。然而,无进展生存期(PFS)与 Bcl-xL 和血小板衍生生长因子受体(PDGFR)-α的表达水平以及单变量分析中存在骨转移和 C 反应蛋白水平显著相关。在这些显著因素中,多变量分析显示 PDGFR-α表达和骨转移的存在与 PFS 独立相关。此外,根据这 2 个独立危险因素的阳性数量,PFS 存在显著差异;即,在无风险因素的 7 例患者中,有 2 例发生疾病进展,在单一风险因素阳性的 34 例患者中,有 19 例发生疾病进展,在两个风险因素均阳性的 6 例患者中,有 6 例发生疾病进展。
综上所述,这些发现表明,考虑潜在分子标志物的表达水平,特别是 PDGFR-α,以及临床参数,可能有助于选择可能从索拉非尼治疗中获益的转移性 RCC 患者。