Low CXCL11 expression is indicative of poor prognosis in rectal cancer patients undergoing preoperative chemoradiotherapy: a retrospective cohort study.

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-11-27 DOI:10.1007/s00428-024-03974-7
Chia-Lin Chou, Cheng-Yi Lin, Wan-Shan Li, Sung-Wei Lee, Ching-Chieh Yang, Yu-Feng Tian, Yow-Ling Shiue, Hsin-Hwa Tsai, Hong-Yue Lai
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Abstract

Introduction: Neoadjuvant concurrent chemoradiotherapy (CCRT) is routinely used before surgery in patients with locally advanced rectal cancer to reduce tumor size and decrease the risk of local recurrence. However, the disease-specific survival has not improved in most cases due to distant metastases. In selected individuals exhibiting a clinical complete response, non-operative management may be allowed; however, those who presented no or little response tend to have an inferior prognosis. Consequently, refined molecular characterization could aid in predicting which patients would benefit from neoadjuvant chemoradiotherapy.

Methods: The mRNA level (by transcriptomic profiling) and protein expression (by immunohistochemical staining) of C-X-C motif chemokine ligand 11 (CXCL11) were integrated to predict neoadjuvant chemoradiotherapy efficacy. For survival analysis, clinicopathological features and CXCL11 immunoreactivity that were statistically significant in univariate analysis were included in multivariate analysis using the Cox proportional hazards regression model.

Results: We identified that the CXCL11 level exhibits the most significant downregulation among neoadjuvant chemoradiotherapy non-responders. Using tumor samples from our rectal cancer cohort (n = 343) with immunohistochemistry validation, we demonstrated that low CXCL11 immunoexpression shows significant correlations with advanced disease and positive lymph nodes both prior to and following CCRT (all p < 0.001), vascular and perineural invasion (p < 0.001 and p = 0.006), and poor response to CCRT (p < 0.001). Moreover, low CXCL11 immunoexpression was an independent adverse prognostic factor significantly associated with patient survival. Additionally, we further identified pyroptotic cell death as an unrevealed role of CXCL11 in rectal cancer through bioinformatic analysis.

Conclusion: CXCL11 expression may serve as an early predictor of clinical outcomes and aid in therapeutic decision-making by identifying individuals likely to respond to neoadjuvant chemoradiotherapy in rectal cancer.

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一项回顾性队列研究:CXCL11低表达提示接受术前放化疗的直肠癌患者预后不良。
简介:新辅助同期化放疗(CCRT)是局部晚期直肠癌患者手术前的常规治疗方法,可缩小肿瘤体积,降低局部复发风险。然而,由于远处转移,大多数病例的疾病特异性生存率并没有提高。对于部分临床反应完全的患者,可以采取非手术治疗;但对于无反应或反应轻微的患者,预后往往较差。因此,精细的分子特征描述有助于预测哪些患者可从新辅助化放疗中获益:方法:综合C-X-C趋化因子配体11(CXCL11)的mRNA水平(通过转录组分析)和蛋白表达(通过免疫组化染色)来预测新辅助化放疗的疗效。在生存率分析中,将单变量分析中具有统计学意义的临床病理特征和CXCL11免疫反应纳入使用Cox比例危险回归模型进行的多变量分析:结果:我们发现,在新辅助化放疗无应答者中,CXCL11水平的下调最为显著。我们利用直肠癌队列中的肿瘤样本(n = 343)进行了免疫组化验证,结果表明,CXCL11的低免疫表达与CCRT前后的晚期疾病和淋巴结阳性有明显的相关性(均为p):CXCL11 的表达可作为临床结果的早期预测指标,并通过识别可能对直肠癌新辅助化放疗产生反应的个体来帮助做出治疗决策。
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
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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