Ustuner Zeki, Saip Pinar, Yasasever Vildan, Vural Burcak, Yazar Aziz, Bal Cengiz, Ozturk Betul, Ozbek Ugur, Topuz Erkan
Department of Medical Oncology, Osmangazi University Medical Faculty, Ataturk Street, Meselik, Eskisehir, 26480, Turkey.
Med Oncol. 2008;25(4):394-9. doi: 10.1007/s12032-008-9052-4. Epub 2008 Mar 4.
Small cell lung cancer (SCLC) has a rapid growth rate and is characterized by early metastases. Tumor growth is dependent on angiogenesis. Vascular endothelial growth factor (VEGF) is an important regulator of angiogenesis. Whether surveillance of pre- and post-treatment serum VEGF and especially its receptors VEGF-1 and VEGF-2 levels in SCLC patients have impact on clinical outcome is unknown.
From February 2001 to January 2003, 39 consecutive patients with histological proven SCLC were enrolled into the study. Pre-treatment (n: 39) and post-treatment (n: 25) samples of the same patients were collected at the time of their response evaluation. The levels of VEGF and its receptors VEGFR-1 and VEGFR-2 were measured in the serum by quantitative sandwich enzyme immunoassay technique.
The median pre-treatment serum VEGF, VEGFR-1, and VEGFR-2 levels which were significantly higher than the normal controls were 1,200 pg/ml (range, 1,414.3 +/- 956.2 pg/ml), 85 pg/ml (range, 97.8 +/- 70.7 pg/ml), and 11,550 pg/ml (range, 14,481 +/- 6,267 pg/ml), respectively. We detected a poor but positive correlation between VEGF and VEGFR-2 (r: 0.46, p: 0.003). Pre-treatment low serum VEGF (<728.5 pg/ml) value (p: 0.02) and good response to treatment (p: 0.008) were found as good prognostic factors by multivariate analysis.
Low serum VEGF concentration is a significant and independent prognostic factor in SCLC patients. Surveillance of VEGF and its receptors to predict chemotherapy response is not useful. Whether the levels of serum VEGF and its receptors VEGFR-1 and VEGFR-2 have value in detecting treatment modalities of SCLC need further studies.
小细胞肺癌(SCLC)生长迅速,其特点是早期转移。肿瘤生长依赖于血管生成。血管内皮生长因子(VEGF)是血管生成的重要调节因子。SCLC患者治疗前和治疗后血清VEGF尤其是其受体VEGF-1和VEGF-2水平的监测是否会影响临床结局尚不清楚。
从2001年2月至2003年1月,39例经组织学证实的SCLC患者连续纳入本研究。在反应评估时收集同一患者的治疗前(n = 39)和治疗后(n = 25)样本。采用定量夹心酶免疫分析技术测定血清中VEGF及其受体VEGFR-1和VEGFR-2的水平。
治疗前血清VEGF、VEGFR-1和VEGFR-2的中位数水平分别为1200 pg/ml(范围为1414.3±956.2 pg/ml)、85 pg/ml(范围为97.8±70.7 pg/ml)和11550 pg/ml(范围为14481±6267 pg/ml),均显著高于正常对照组。我们检测到VEGF与VEGFR-2之间存在弱但为正的相关性(r = 0.46,p = 0.003)。多因素分析发现,治疗前血清VEGF低水平(<728.5 pg/ml)(p = 0.02)和对治疗反应良好(p = 0.008)是良好的预后因素。
血清VEGF浓度低是SCLC患者的一个重要且独立的预后因素。监测VEGF及其受体以预测化疗反应并无用处。血清VEGF及其受体VEGFR-1和VEGFR-2水平在检测SCLC治疗方式方面是否有价值需要进一步研究。