Santini Daniele, Vincenzi Bruno, Dicuonzo Giordano, Avvisati Giuseppe, Massacesi Cristian, Battistoni Fabrizio, Gavasci Michele, Rocci Laura, Tirindelli Maria Cristina, Altomare Vittorio, Tocchini Massimo, Bonsignori Maurizio, Tonini Giuseppe
Medical Oncology, Department of Laboratory Medicine, Campus Bio-Medico University, 00155 Rome, Italy.
Clin Cancer Res. 2003 Aug 1;9(8):2893-7.
The commercial availability of zoledronic acid, a third generation bisphosphonate, prompted us to evaluate the modifications in angiogenic cytokines levels after a single i.v. infusion of this drug.
Thirty consecutive cancer patients with scintigraphic and radiographic evidence of bone metastases were treated with a single infusion of 4 mg of zoledronic acid before any chemotherapy. The patients were prospectively evaluated for circulating levels of vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF) just before and at 1, 2, 7, and 21 days after zoledronic acid infusion.
Basal serum VEGF median levels were significantly decreased at days 2 (-23%), 7 (-28%), and 21 (-34%) after zoledronic acid infusion (P = 0.0498, 0.0090, and 0.0011, respectively). Serum PDGF levels were significantly decreased by 25% 1 day after zoledronic acid infusion (P = 0.0032). This effect on circulating PDGF levels persisted for 2 days after bisphosphonate infusion (P = 0.0050). PDGF levels had returned to values similar to the median basal value at 7 and 21 days. Moreover, a linear regression model with variance analysis showed a significant positive correlation between basal VEGF and PDGF values but not at the following time points. No significant differences were recorded in platelet levels, WBC count, or hemoglobin concentration before and after zoledronic acid single infusion.
This study confirms that zoledronic acid could have an in vivo antiangiogenic property through a significant and long-lasting reduction in serum VEGF levels.
第三代双膦酸盐唑来膦酸的商业可得性促使我们评估单次静脉输注该药物后血管生成细胞因子水平的变化。
30例连续的有骨转移闪烁扫描和放射影像学证据的癌症患者在任何化疗之前接受单次4mg唑来膦酸输注。在唑来膦酸输注前、输注后1天、2天、7天和21天对患者循环中的血管内皮生长因子(VEGF)和血小板衍生生长因子(PDGF)水平进行前瞻性评估。
唑来膦酸输注后第2天(-23%)、第7天(-28%)和第21天(-34%),基础血清VEGF中位数水平显著降低(P分别为0.0498、0.0090和0.0011)。唑来膦酸输注后1天血清PDGF水平显著降低25%(P = 0.0032)。双膦酸盐输注后这种对循环PDGF水平的影响持续2天(P = 0.0050)。在第7天和第21天,PDGF水平已恢复至与基础中位数水平相似的值。此外,方差分析的线性回归模型显示基础VEGF和PDGF值之间存在显著正相关,但在随后的时间点不存在。唑来膦酸单次输注前后血小板水平、白细胞计数或血红蛋白浓度无显著差异。
本研究证实唑来膦酸可通过显著且持久地降低血清VEGF水平而具有体内抗血管生成特性。