Nakamura H, Kawasaki N, Taguchi M, Kabasawa K
Department of Chest Surgery, Atami Hospital, International University of Health and Welfare, 13-1 Higashikaigan-cho, Atami-shi, Shizuoka, 413-0012 Japan.
Thorax. 2006 Feb;61(2):140-5. doi: 10.1136/thx.2005.042275. Epub 2005 Nov 11.
It is thought that overexpression of epidermal growth factor receptor (EGFR) in non-small cell lung cancer (NSCLC) might compromise patient survival, presumably by promoting tumour growth by an autocrine mechanism. However, conflicting results have been reported from various laboratories, and the clinical importance of EGFR overexpression remains unsettled.
A meta-analysis of previous studies was performed to quantitatively review the effects of EGFR overexpression on survival in patients with NSCLC using a DerSimonian-Laird random effects model. Eighteen studies including 2972 patients were subjected to final analysis.
Overall, positivity for EGFR overexpression differed between histological types: 39% in adenocarcinomas, 58% in squamous cell carcinomas, 38% in large cell carcinomas, and 32% in cancers in a miscellaneous category (p<0.0001). The combined hazard ratio (HR) was 1.14 (95% CI 0.97 to 1.34; p = 0.103), indicating that EGFR overexpression has no significant impact on survival. When only the 15 immunohistochemistry based studies were considered, the combined HR was 1.08 (95% CI 0.92 to 1.28; p = 0.356), again suggesting that EGFR overexpression has no impact on survival. Heterogeneity testing indicated that there was heterogeneity between studies but publication bias was absent, which suggests that the summary statistics obtained may approximate the actual average.
EGFR overexpression was not associated with poorer survival in patients with NSCLC. Specific mutations of the EGFR gene will need further study in terms of survival implications.
人们认为,非小细胞肺癌(NSCLC)中表皮生长因子受体(EGFR)的过表达可能会影响患者的生存率,推测其通过自分泌机制促进肿瘤生长。然而,各个实验室报告的结果相互矛盾,EGFR过表达的临床重要性仍未确定。
对先前的研究进行荟萃分析,使用DerSimonian-Laird随机效应模型定量评估EGFR过表达对NSCLC患者生存率的影响。最终分析纳入了18项研究,共2972例患者。
总体而言,EGFR过表达的阳性率在不同组织学类型之间存在差异:腺癌为39%,鳞状细胞癌为58%,大细胞癌为38%,其他类型癌症为32%(p<0.0001)。合并风险比(HR)为1.14(95%CI 0.97至1.34;p = 0.103),表明EGFR过表达对生存率无显著影响。仅考虑15项基于免疫组织化学的研究时,合并HR为1.08(95%CI 0.92至1.28;p = 0.356),再次表明EGFR过表达对生存率无影响。异质性检验表明研究之间存在异质性,但不存在发表偏倚,这表明获得的汇总统计数据可能接近实际平均值。
EGFR过表达与NSCLC患者较差的生存率无关。EGFR基因的特定突变对生存的影响需要进一步研究。