Centre for Experimental Cancer Medicine, St Bartholomew's Hospital.
Department of Medical Oncology, Guys' and St Thomas Hospital.
Ann Oncol. 2011 Apr;22(4):815-820. doi: 10.1093/annonc/mdq469. Epub 2010 Oct 13.
Haematopoietic progenitor cells (HPCs) are present in blood in metastatic renal cell cancer (mRCC). We investigate their expression in mRCC patients treated with sunitinib and correlate their expression with plasma growth factor levels [insulin-like growth factor (IGF)-1].
Circulating HPCs (CD34(+)/CD45(+)) and plasma IGF-1 levels were measured at specific sequential time points (0, 6, 18 and 28 weeks) in 43 untreated mRCC patients receiving sunitinib (50 mg for 28 days followed by 14-day off treatment). Univariate and multivariate analysis assessed the prognostic significance of HPCs and IGF-1.
HPCs levels were raised in 40 of 43 (93%) of patients. IGF-1 levels were raised in 9 of 43 patients (21%). Univariate and multivariate analysis revealed that high HPCs before treatment were associated with a significantly shorter overall survival (hazard ratio 3.3, 95% confidence interval 1.23-8.8, P=0.01), which was not the case for IGF-1 levels. Both HPC and IGF-1 levels fell with sunitinib (61% and 14% fall, respectively, P <0.05 for both). A positive correlation between the falls in HPC and IGF-1 occurred (P<0.001).
HPCs are over expressed in the peripheral blood in the majority of patients with mRCC. Higher levels are associated with poor prognosis. A concurrent fall in HPCs and growth factor expression (IGF-1) with sunitinib occurs.
造血祖细胞(HPC)存在于转移性肾细胞癌(mRCC)患者的血液中。我们研究了它们在接受舒尼替尼治疗的 mRCC 患者中的表达情况,并将其表达与血浆生长因子水平[胰岛素样生长因子(IGF)-1]相关联。
在 43 名未接受治疗的接受舒尼替尼(28 天 50mg 治疗,随后 14 天停药)的 mRCC 患者中,在特定的时间点(0、6、18 和 28 周)测量循环 HPC(CD34(+)/CD45(+))和血浆 IGF-1 水平。单变量和多变量分析评估了 HPC 和 IGF-1 的预后意义。
43 名患者中有 40 名(93%)患者的 HPC 水平升高。9 名患者(21%)的 IGF-1 水平升高。单变量和多变量分析显示,治疗前 HPC 水平较高与总生存率显著缩短相关(危险比 3.3,95%置信区间 1.23-8.8,P=0.01),而 IGF-1 水平则不然。舒尼替尼可降低 HPC 和 IGF-1 水平(分别下降 61%和 14%,均 P<0.05)。HPC 和 IGF-1 下降之间存在正相关(P<0.001)。
在大多数 mRCC 患者的外周血中,HPC 过度表达。较高的水平与预后不良相关。舒尼替尼可同时降低 HPC 和生长因子表达(IGF-1)。