CD44, SHH and SOX2 as novel biomarkers in esophageal cancer patients treated with neoadjuvant chemoradiotherapy

被引:18
作者
Honing, Judith [1 ]
Pavlov, Kirill V. [2 ]
Mul, Veronique E. M. [3 ]
Karrenbeld, Arend [4 ]
Meijer, Coby [5 ]
Faiz, Zohra [1 ]
Smit, Justin K. [1 ]
Hospers, Geke A. P. [5 ]
Burgerhof, Johannes G. M. [6 ]
Kruyt, Frank A. E. [5 ]
Kleibeuker, Jan H. [2 ]
Plukker, John T. M. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Surg, NL-9700 AB Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Gastroenterol & Hepatol, NL-9700 AB Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Radiat Oncol, NL-9700 AB Groningen, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol, NL-9700 AB Groningen, Netherlands
[5] Univ Groningen, Univ Med Ctr Groningen, Dept Med Oncol, NL-9700 AB Groningen, Netherlands
[6] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, NL-9700 AB Groningen, Netherlands
关键词
Esophageal; Cancer; Stem cell biomarkers; Neoadjuvant; Chemoradiotherapy; STEM-CELL MARKERS; PREOPERATIVE CHEMORADIOTHERAPY; BARRETTS-ESOPHAGUS; HEDGEHOG; ADENOCARCINOMA; EXPRESSION; RADIOTHERAPY; PREDICTION; PROGNOSIS;
D O I
10.1016/j.radonc.2015.08.031
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: Neoadjuvant chemoradiotherapy (nCRT) improves survival in esophageal cancer (EC) patients, but the response to treatment is heterogeneous and little is known regarding prognostic and predictive markers in these patients. CD44, SOX2 and SHH have been implicated in resistance to CRT, possibly through an association with a cancer stem cell phenotype. Material and methods: 101 EC patients treated with nCRT and surgery were included. Sufficient pretreatment biopsy material was present in 71 patients, of which 53 patients were non-complete responders on nCRT (nCR). Protein expression was examined using immunohistochemistry (IHC). Prognostic factors were determined using Cox regression analysis for disease free survival (DFS) and cause specific survival (CSS) in the complete cohort, the pre-treatment biopsies group and post-treatment nCR group. Results: Low CD44 expression in the nCR group was an independent prognostic factor for both DFS and CSS (DFS HR 2.81, p = 0.002 and CSS HR 3.48, p = 0.002). Absent SOX2 expression in pretreatment biopsies was related to systemic recurrence (p = 0.029) while low,SHH in pretreatment biopsies was an independent prognostic factor for a poor DES (HR 2.27, p = 0.036). No relation between marker expression and response to nCRT was observed. Conclusions: Low expression of CD44 and SHH are associated with a poor survival outcome in EC patients treated with nCRT. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:152 / 158
页数:7
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