Department of Oncology and Radiotherapy, Charles University Medical School and Teaching Hospital, Hradec Kralove, Czech Republic.
Strahlenther Onkol. 2012 Sep;188(9):833-8. doi: 10.1007/s00066-012-0160-x. Epub 2012 Aug 1.
The aim of the present study was to examine the effect of neoadjuvant chemoradiation on tumor epidermal growth factor receptor (EGFR) expression in patients with locally advanced rectal adenocarcinoma.
A total of 53 patients with rectal adenocarcinoma (clinical stages II and III) were studied. Neoadjuvant treatment consisted of 50.4 Gy/28 fractions external radiation with concomitant continuous 5-fluorouracil. Surgical resection was performed 4-6 weeks after the chemoradiation. EGFR expression in the pretreatment biopsies and in the resected specimens was assessed with immunohistochemistry.
Patients with an increase of EGFR expression during chemoradiation had significantly shorter disease-free survival (DFS; p = 0.003) and overall survival (OS; p = 0.005) compared to patients with either no change or decrease in EGFR expression. The 5-year DFS in patients with increased EGFR expression was only 29% compared to 61% in patients without an increase of EGFR expression. Similarly, the 5-year OS of the patients with increased EGFR expression was 29% compared to 66% in patients without an increase of EGFR expression. All recurrences in patients who had an increase of EGFR expression occurred within the first 2 years after the treatment. The increase in EGFR expression was the only significant predictor of DFS (p = 0.007) and OS (p = 0.04) using multivariate Cox regression analysis.
An increase of EGFR expression during chemoradiation may be associated with significantly shorter DFS and OS. The increase of EGFR could identify a population of patients in whom the effect of the treatment with anti-EGFR therapy should be studied.
本研究旨在探讨新辅助放化疗对局部晚期直肠腺癌患者肿瘤表皮生长因子受体(EGFR)表达的影响。
共纳入 53 例直肠腺癌(临床分期 II 和 III 期)患者。新辅助治疗包括 50.4 Gy/28 次外照射,同时持续给予 5-氟尿嘧啶。放化疗后 4-6 周行手术切除。采用免疫组织化学法检测术前活检和切除标本中 EGFR 的表达。
与 EGFR 表达无变化或下降的患者相比,放化疗过程中 EGFR 表达增加的患者无病生存(DFS;p = 0.003)和总生存(OS;p = 0.005)显著缩短。EGFR 表达增加患者的 5 年 DFS 仅为 29%,而 EGFR 表达无增加患者的 5 年 DFS 为 61%。同样,EGFR 表达增加患者的 5 年 OS 为 29%,而 EGFR 表达无增加患者的 5 年 OS 为 66%。所有 EGFR 表达增加的患者的复发均发生在治疗后 2 年内。多变量 Cox 回归分析显示,EGFR 表达增加是 DFS(p = 0.007)和 OS(p = 0.04)的唯一显著预测因素。
放化疗过程中 EGFR 表达增加可能与 DFS 和 OS 显著缩短相关。EGFR 表达增加可识别出一个需要研究抗 EGFR 治疗效果的患者群体。