Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Cancer. 2011 Jan 1;117(1):143-51. doi: 10.1002/cncr.25560. Epub 2010 Aug 27.
In patients with nonsmall cell lung cancer (NSCLC), several studies have demonstrated a positive correlation between somatic mutation in the epidermal growth factor receptor (EGFR) tyrosine kinase domain and clinical outcomes with the use of EGFR tyrosine kinase inhibitors (TKIs). However, some patients with wild-type (WT) EGFR also responded to EGFR TKIs and remained stable. Recently, amphiregulin (AR) has been suggested as a predictive marker for EGFR TKIs in patients with WT EGFR-positive NSCLC. The objective of the current study was to evaluate the association between AR expression and the efficacy of using EGFR TKIs in the treatment of patients with WT EGFR-positive NSCLC.
Seventy-three patients with WT EGFR-positive NSCLC received treatment with gefitinib or erlotinib between May 2005 and December 2008. AR expression was assessed by immunohistochemistry.
The clinical response to EGFR TKIs was reassessed for all patients as follows: 16 of 73 patients had a partial response (21.9%), 12 patients had stable disease (16.5%), and 45 patients had progressive disease (61.6%). AR expression was positive in 24 of 40 patients (60%). The ability to achieve disease control did not differ significantly between AR-positive patients and AR-negative patients (P = .188). At a median follow-up of 25.4 months (range, 10.5-53.3 months), progression-free survival was 8.1 weeks in AR-positive patients and 4 weeks in AR-negative patients (P = .025), and overall survival was significantly longer in AR-positive patients than in AR-negative patients (12.2 months vs 4.1 months; P = .001).
The current results suggested that patients with WT EGFR-positive NSCLC who have AR-positive tumors may benefit clinically from treatment with EGFR TKIs, indicating that AR expression may be a potential marker for the selection of EGFR-TKI treatment for patients with WT EGFR-positive NSCLC.
在非小细胞肺癌(NSCLC)患者中,几项研究表明表皮生长因子受体(EGFR)酪氨酸激酶结构域的体细胞突变与 EGFR 酪氨酸激酶抑制剂(TKI)的临床疗效之间存在正相关。然而,一些 EGFR 野生型(WT)的患者也对 EGFR TKI 有反应,并保持稳定。最近, Amphiregulin(AR)被认为是 WT EGFR 阳性 NSCLC 患者中 EGFR TKI 的预测标志物。本研究的目的是评估 AR 表达与 WT EGFR 阳性 NSCLC 患者使用 EGFR TKI 治疗疗效之间的关系。
2005 年 5 月至 2008 年 12 月期间,73 例 WT EGFR 阳性 NSCLC 患者接受吉非替尼或厄洛替尼治疗。通过免疫组织化学评估 AR 表达。
对所有患者重新评估 EGFR TKI 的临床反应如下:73 例患者中,16 例(21.9%)有部分缓解,12 例(16.5%)病情稳定,45 例(61.6%)病情进展。40 例患者中有 24 例(60%)AR 表达阳性。AR 阳性患者和 AR 阴性患者达到疾病控制的能力无显著差异(P=0.188)。中位随访时间为 25.4 个月(范围为 10.5-53.3 个月),AR 阳性患者无进展生存期为 8.1 周,AR 阴性患者为 4 周(P=0.025),AR 阳性患者总生存期明显长于 AR 阴性患者(12.2 个月 vs 4.1 个月;P=0.001)。
目前的结果表明,WT EGFR 阳性 NSCLC 患者中 AR 阳性肿瘤的患者可能从 EGFR TKI 治疗中获益,表明 AR 表达可能是选择 WT EGFR 阳性 NSCLC 患者进行 EGFR-TKI 治疗的潜在标志物。