Division of Colon and Rectal Surgery, Department of Surgery, St Luke's-Roosevelt Hospital Center, Suite 7B, 425 West 59th Street, New York, NY 10019, USA.
Surg Endosc. 2010 Oct;24(10):2617-22. doi: 10.1007/s00464-010-1018-x. Epub 2010 Mar 31.
Epidermal growth factor (EGF) stimulates tumor growth directly via tumor cell EGF receptors or indirectly via its proangiogenic effects. This study's purpose was to determine the impact of minimally invasive colorectal resection (MICR) on postoperative (postop) plasma EGF levels in the colorectal cancer (CRC) and benign disease settings and to see if preoperative (PreOp) EGF levels are altered in cancer patients.
MICR patients with benign pathology (n = 40) and CRC (n = 48) had blood samples taken PreOp and on postoperative days (POD) 1 and 3. In some patients, late samples were taken between POD7 and POD60; these were bundled into 7-day blocks and considered as single time points. EGF levels were determined by enzyme-linked immunosorbent assay (ELISA) and results were reported as mean ± SD after logarithmic transformation. The Student t test was used (p < 0.008 after Bonferroni correction).
The cancer and benign groups were comparable except for age. The mean PreOp CRC plasma EGF level (122.9 ± 75.9 pg/ml) was significantly higher than that of the benign group (85.3 ± 38.5 pg/ml) (p = 0.015). The cancer group's EGF levels were significantly decreased on POD1 and POD3 and for the POD31-55 time point (mean EGF level = 63.1 ± 42.2 (n = 10). The benign group's POD3 and POD7-14 EGF levels were significantly lower than the PreOp level; later levels returned toward baseline. Small late sample size limited analysis.
Plasma EGF levels are significantly higher in cancer patients. MICR is associated with a significant decrease in EGF levels early postop in both cancer and benign settings. Unlike the benign group, EGF blood levels in cancer patients remain low during the second postop month. A larger study with more late samples is needed to verify these results. EGF may have value as a tumor marker.
表皮生长因子(EGF)通过肿瘤细胞 EGF 受体直接刺激肿瘤生长,或通过其促血管生成作用间接刺激肿瘤生长。本研究旨在确定微创结直肠切除术(MICR)对结直肠癌(CRC)和良性疾病患者术后(postop)血浆 EGF 水平的影响,并观察癌症患者术前(PreOp)EGF 水平是否发生改变。
对良性病理(n=40)和 CRC(n=48)患者进行 MICR,分别在术前(PreOp)和术后第 1 天(POD1)及第 3 天(POD3)采血。部分患者在 POD7 至 POD60 之间采集晚期样本,将这些样本捆绑为 7 天一组,视为单个时间点。采用酶联免疫吸附试验(ELISA)测定 EGF 水平,经对数转换后以平均值±标准差表示。采用 Student t 检验(Bonferroni 校正后 p < 0.008)。
CRC 组和良性组除年龄外,其他方面无差异。CRC 组患者术前(PreOp)血浆 EGF 水平(122.9±75.9pg/ml)显著高于良性组(85.3±38.5pg/ml)(p=0.015)。CRC 组患者术后第 1 天和第 3 天,以及术后第 31-55 天(平均 EGF 水平=63.1±42.2(n=10)EGF 水平明显降低。良性组患者术后第 3 天和第 7-14 天 EGF 水平明显低于术前(PreOp)水平,后期水平恢复至基线。由于晚期样本量较小,限制了分析。
癌症患者的血浆 EGF 水平显著升高。MICR 后,CRC 患者和良性疾病患者的 EGF 水平在术后早期均显著下降。与良性组不同,癌症患者在术后第二个月,EGF 血水平仍较低。需要进行更大规模的研究,纳入更多晚期样本,以验证这些结果。EGF 可能作为肿瘤标志物具有一定价值。