Foroughi Siavash, Hutchinson Ryan A, Wong Hui-Li, Christie Michael, Batrouney Ahida, Wong Rachel, Lee Margaret, Tie Jeanne, Burgess Antony Wilks, Gibbs Peter
Personalised Oncology Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Department of Medical Biology, The University of Melbourne, Parkville, Victoria, Australia.
Growth Factors. 2020 Jun-Jul;38(3-4):127-136. doi: 10.1080/08977194.2021.1878166. Epub 2021 Mar 27.
For patients with metastatic colorectal cancer (mCRC), epidermal growth factor receptor (EGFR) inhibitors are limited to patients with wild-type tumours. Not all patients will benefit from treatment and better predictive biomarkers are needed. Here we investigated the prognostic and predictive impact of the EGFR ligands amphiregulin (AREG) and epiregulin (EREG). Expression levels were assessed by immunohistochemistry on 99 wild-type tumours. AREG and EREG positivity was seen in 49% and 50% of cases, respectively. No difference in expression was observed by primary tumour side. There was no significant difference in OS by AREG or EREG expression. In the subset of patients who received an EGFR inhibitor, EREG positivity was associated with longer OS (median 34.0 vs. 27.0 months, = 0.033), driven by a difference in patients with a left-sided primary (HR 0.37, = 0.015). Our study supports further investigation into EREG as a predictive biomarker in mCRC.
对于转移性结直肠癌(mCRC)患者,表皮生长因子受体(EGFR)抑制剂仅限于野生型肿瘤患者。并非所有患者都能从治疗中获益,因此需要更好的预测生物标志物。在此,我们研究了EGFR配体双调蛋白(AREG)和表皮调节素(EREG)的预后和预测作用。通过免疫组织化学对99例野生型肿瘤评估表达水平。AREG和EREG阳性分别见于49%和50%的病例。原发肿瘤部位未观察到表达差异。AREG或EREG表达对总生存期无显著差异。在接受EGFR抑制剂治疗的患者亚组中,EREG阳性与更长的总生存期相关(中位生存期34.0个月对27.0个月,P = 0.033),这是由左侧原发肿瘤患者的差异所驱动的(风险比0.37,P = 0.015)。我们的研究支持进一步研究EREG作为mCRC的预测生物标志物。