Department of Clinical Therapeutics, University of Athens, Athens, Greece.
Int J Gynecol Cancer. 2010 Feb;20(2):248-54. doi: 10.1111/IGC.0b013e3181cc25c3.
Serum CD105 has been associated with angiogenic activity in cancer, and low CD105 expression has been associated with improved prognosis. The present study evaluated the prognostic significance of serum levels of CD105 and related factors in patients with epithelial ovarian cancer (EOC) after cytoreductive surgery and chemotherapy.
Eighty-six patients with stages IIC to IV EOC treated postoperatively with platinum-based chemotherapy were included. The enzyme-linked immunosorbent assay was used to measure prechemotherapy serum levels of CD105, transforming growth factor beta1/2 (TGF-beta1/2), angiopoietin 2, vascular endothelial growth factor, and tumor necrosis factor-alpha.
High levels of TGF-beta2 (>8908.86 pg/mL) and CD105 (>4.25 ng/mL) were independently associated with improved overall survival (not reached vs 39 months, P = 0.009 and 75 vs 39 months, P = 0.029, respectively), whereas a high level of TGF-beta2 and a low level of vascular endothelial growth factor (<219.04 pg/mL) were independently associated with improved progression-free survival (49 vs 17 months, P = 0.022 and 57 vs 16 months, P = 0.023, respectively). Among patients with favorable (>4.25 ng/mL) CD105 levels, only patients with low TGF-beta1 levels (<177.1 ng/mL) had superior survival than patients with low CD105 levels.
Our study confirms the prognostic significance of angiogenesis in EOC and supports a biological interaction between CD105 and TGF-beta1. High angiogenic activity may be associated by increased efficacy of postoperative chemotherapy.
血清 CD105 与癌症中的血管生成活性有关,低 CD105 表达与改善预后有关。本研究评估了细胞减灭术后化疗后上皮性卵巢癌(EOC)患者血清 CD105 水平及其相关因素的预后意义。
纳入 86 例接受铂类化疗的 IIC 至 IV 期 EOC 术后患者。采用酶联免疫吸附试验检测化疗前血清 CD105、转化生长因子β1/2(TGF-β1/2)、血管生成素 2、血管内皮生长因子和肿瘤坏死因子-α水平。
高水平 TGF-β2(>8908.86 pg/mL)和 CD105(>4.25 ng/mL)与总生存时间延长独立相关(未达到 vs 39 个月,P=0.009 和 75 vs 39 个月,P=0.029),而高水平 TGF-β2 和低水平血管内皮生长因子(<219.04 pg/mL)与无进展生存时间延长独立相关(49 vs 17 个月,P=0.022 和 57 vs 16 个月,P=0.023)。在 CD105 水平较好(>4.25 ng/mL)的患者中,仅 TGF-β1 水平较低(<177.1 ng/mL)的患者的生存状况优于 CD105 水平较低的患者。
本研究证实了血管生成在 EOC 中的预后意义,并支持 CD105 和 TGF-β1 之间的生物学相互作用。高血管生成活性可能与术后化疗疗效增加有关。