Immunohistochemical evaluation of the prognostic and predictive power of epidermal growth factor receptor ligand levels in patients with metastatic colorectal cancer.

IF 1.8 4区 生物学 Q4 CELL BIOLOGY
Growth factors Pub Date : 2020-06-01 Epub Date: 2021-03-27 DOI:10.1080/08977194.2021.1878166
Siavash Foroughi, Ryan A Hutchinson, Hui-Li Wong, Michael Christie, Ahida Batrouney, Rachel Wong, Margaret Lee, Jeanne Tie, Antony Wilks Burgess, Peter Gibbs
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引用次数: 0

Abstract

For patients with metastatic colorectal cancer (mCRC), epidermal growth factor receptor (EGFR) inhibitors are limited to patients with RAS 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 KRAS 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, p = 0.033), driven by a difference in patients with a left-sided primary (HR 0.37, p = 0.015). Our study supports further investigation into EREG as a predictive biomarker in mCRC.

转移性结直肠癌患者表皮生长因子受体配体水平的预后和预测能力的免疫组织化学评估。
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RAS野生型肿瘤患者。并非所有患者都能从治疗中受益,需要更好的预测性生物标志物。在这里,我们研究了EGFR配体双调节蛋白(AREG)和表调节蛋白(EREG)的预后和预测作用。采用免疫组化方法检测99例KRAS野生型肿瘤的表达水平。AREG和EREG阳性分别占49%和50%。原发肿瘤侧的表达无差异。AREG和EREG表达差异无统计学意义。在接受EGFR抑制剂的患者亚组中,EREG阳性与更长的生存期相关(中位34.0个月vs. 27.0个月,p = 0.033),这是由左侧原发患者的差异驱动的(HR 0.37, p = 0.015)。我们的研究支持进一步研究EREG作为mCRC的预测性生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Growth factors
Growth factors 生物-内分泌学与代谢
CiteScore
2.60
自引率
0.00%
发文量
20
审稿时长
>12 weeks
期刊介绍: Growth Factors is an international and interdisciplinary vehicle publishing new knowledge and findings on the regulators of cell proliferation, differentiation and survival. The Journal will publish research papers, short communications and reviews on current developments in cell biology, biochemistry, physiology or pharmacology of growth factors, cytokines or hormones which improve our understanding of biology or medicine. Among the various fields of study topics of particular interest include: •Stem cell biology •Growth factor physiology •Structure-activity relationships •Drug development studies •Clinical applications
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