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卵巢癌一线治疗期间血小板衍生生长因子受体β血清浓度。

Platelet-derived growth factor receptor beta serum concentrations during first-line therapy in ovarian cancer.

机构信息

Department of Gynecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Oncology. 2013;85(2):69-77. doi: 10.1159/000351032. Epub 2013 Jul 16.

Abstract

OBJECTIVES

Angiogenesis plays an important role in ovarian cancer. The interaction of platelet-derived growth factor receptor-beta (PDGFR-β) with vascular endothelial growth factor (VEGF) in the process of angiogenesis may represent an essential feature in the progression of the disease.

METHODS

Patients with epithelial ovarian cancer, who underwent primary surgery and platinum-based first-line chemotherapy, were included. A total of 133 serum samples from 39 patients were analyzed. Samples were prospectively collected at 4 time points: (1) before surgery, (2) after surgery and before chemotherapy, (3) during chemotherapy and (4) after chemotherapy. Serum PDGFR-β was quantified by ELISA. We analyzed the correlation of serum levels to chemotherapy response, progression-free and overall survival (PFS and OS) and the serum markers CA-125 and VEGF-165.

RESULTS

Serum concentration of PDGFR-β ranged between 4 and 72 ng/ml and increased significantly during first-line chemotherapy (p = 0.019). PDGFR-β serum concentrations showed an inverse correlation with CA-125 and VEGF-165 after chemotherapy (r = -0.495, p = 0.003 and r = -0.345, p = 0.04, respectively). Increased PDGFR-β serum levels after chemotherapy were significantly correlated with better PFS (p = 0.026) and OS (p = 0.013) in a univariate analysis.

CONCLUSION

PDGFR-β might be a useful biomarker in terms of prognosis and could be important as antiangiogenic agents become a component of standard treatment in ovarian cancer.

摘要

目的

血管生成在卵巢癌中起着重要作用。血小板衍生生长因子受体-β(PDGFR-β)与血管内皮生长因子(VEGF)在血管生成过程中的相互作用可能代表疾病进展的一个重要特征。

方法

纳入接受初次手术和基于铂类的一线化疗的上皮性卵巢癌患者。共分析了 39 例患者的 133 份血清样本。前瞻性地在 4 个时间点采集样本:(1)手术前,(2)手术后和化疗前,(3)化疗期间,(4)化疗后。通过 ELISA 定量检测血清 PDGFR-β。我们分析了血清水平与化疗反应、无进展生存期(PFS)和总生存期(OS)以及血清标志物 CA-125 和 VEGF-165 的相关性。

结果

PDGFR-β 的血清浓度范围为 4 至 72ng/ml,在一线化疗期间显著升高(p=0.019)。化疗后 PDGFR-β 血清浓度与 CA-125 和 VEGF-165 呈负相关(r=-0.495,p=0.003 和 r=-0.345,p=0.04)。化疗后 PDGFR-β 血清水平升高与 PFS(p=0.026)和 OS(p=0.013)的改善显著相关。

结论

PDGFR-β 可能是一种有用的预后生物标志物,并且在抗血管生成药物成为卵巢癌标准治疗的一部分时可能很重要。

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