University Department of Surgery, Faculty of Medicine-University of Glasgow, Royal Infirmary, Alexandra parade, Glasgow G31 2ER, UK.
Clin Nutr. 2010 Apr;29(2):206-9. doi: 10.1016/j.clnu.2009.08.013. Epub 2009 Sep 11.
BACKGROUND & AIMS: The involvement of a systemic inflammatory response, as evidenced by the Glasgow Prognostic Score (GPS), is associated with weight loss and poor outcome in patients with non-small cell lung cancer. There is good evidence that nutritional and functional decline in patients with advanced malignant disease is associated with catabolic changes in metabolism. However, defects in anabolism may also contribute towards nutritional decline in patients with cancer. The aim of the present study was to examine the relationship between IGF-1 and IGFBP-3, performance status, mGPS and survival in patients with inoperable NSCLC.
56 patients with inoperable NSCLC were studied. The plasma concentrations of IGF-1, IGFBP-3 and leptin were measured using ELISA and RIA.
The patients were predominantly male (61%), over 60 years old (80%), with advanced (stage III or IV) disease (98%), with a BMI> or =20 (84%), an ECOG-ps of 0 or 1 (79%), a haemoglobin (59%) and white cell count (79%) in the reference range. On follow-up 43 patients died of their cancer. On univariate analysis, BMI (p<0.05), Stage (p<0.05), ECOG-ps (p<0.05), haemoglobin (p<0.05), white cell count (p<0.05) and mGPS (p<0.05) were associated with cancer specific survival. There was no association between age, sex, treatment, IGF-1, IGFBP-3, IGF-1:IGFBP-3 ratio, or leptin and cancer specific survival. With an increasing mGPS concentrations of haemoglobin (p<0.005) and IGFBP-3 (p<0.05) decreased. mGPS was not associated with either IGF-1(p>0.20), or leptin (p>0.20).
In summary, the results of this study suggest that anabolism (IGF-1 axis) does not play a significant role in the relationship between nutritional and functional decline, systemic inflammation and poor survival in patients with inoperable NSCLC.
全身炎症反应的参与,如格拉斯哥预后评分(GPS)所证明的,与非小细胞肺癌患者的体重减轻和不良预后相关。有充分的证据表明,晚期恶性疾病患者的营养和功能下降与代谢的分解代谢变化有关。然而,合成代谢的缺陷也可能导致癌症患者的营养下降。本研究的目的是检查不可切除的非小细胞肺癌患者中 IGF-1 和 IGFBP-3、体能状态、mGPS 和生存之间的关系。
研究了 56 例不可切除的非小细胞肺癌患者。使用 ELISA 和 RIA 测量 IGF-1、IGFBP-3 和瘦素的血浆浓度。
患者主要为男性(61%),年龄超过 60 岁(80%),患有晚期(III 或 IV 期)疾病(98%),BMI≥20(84%),ECOG-ps 为 0 或 1(79%),血红蛋白(59%)和白细胞计数(79%)在参考范围内。在随访中,43 例患者死于癌症。单因素分析显示,BMI(p<0.05)、分期(p<0.05)、ECOG-ps(p<0.05)、血红蛋白(p<0.05)、白细胞计数(p<0.05)和 mGPS(p<0.05)与癌症特异性生存相关。年龄、性别、治疗、IGF-1、IGFBP-3、IGF-1:IGFBP-3 比值或瘦素与癌症特异性生存之间无相关性。随着 mGPS 浓度的增加,血红蛋白(p<0.005)和 IGFBP-3(p<0.05)降低。mGPS 与 IGF-1(p>0.20)或瘦素(p>0.20)均无相关性。
总之,本研究结果表明,在不可切除的非小细胞肺癌患者中,合成代谢(IGF-1 轴)在营养和功能下降、全身炎症反应和不良预后之间的关系中不起重要作用。