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是否存在能够确定直肠癌新辅助治疗反应的预测指标?

Are there predictors that can determine neoadjuvant treatment responses in rectal cancer?

作者信息

Yılmaz Rakıcı Sema, Bedir Recep, Hatipoğlu Celile

机构信息

Department of Radiation Oncology, Recep Tayyip Erdoğan University School of Medicine, Rize, Turkey.

Department of Medical Pathology, Recep Tayyip Erdoğan University School of Medicine, Rize, Turkey.

出版信息

Turk J Gastroenterol. 2019 Mar;30(3):220-227. doi: 10.5152/tjg.2018.18179.

Abstract

BACKGROUND/AIMS: This study aimed to determine a predictive bioindicator that would detect the treatment response of patients diagnosed with rectal cancer and treated with neoadjuvant chemoradiotherapy (nCRT).

MATERIALS AND METHODS

The data collected from 37 patients receiving nCRT were retrospectively evaluated. The p53 score and gene instability in MLH1 and MSH2, which are among the DNA mismatch repair (MMR) genes, were evaluated using immunohistochemical methods. The neutrophils-leukocytes ratio (NLR), carcinoembryonic antigen (CEA), and carbohydrate antigen (CA) 19-9 values were obtained as hematological parameters from computer records. The pathologic analysis of the therapy response after nCRT was classified according to the modified grading system by Ryan et al. Results: The changes in the NLR, CEA, and CA19-9 values before and after treatment were statistically significant (p<0.001 and p=0.005). A near significant effect of the decrease of the CEA value in the 5th week after treatment was detected on the pathological response score (p=0.075). The p53 mutation score in those patients with any residue was higher than the total response. Overall, 89.2% of the patients exhibited MMR positivity (stability), and 10.8% of the cases with MRM negativity (instability) had a macroscopic residue. Cases with pathological total response were MRM positive.

CONCLUSION

Consequently, in most of the patients treated with nCRT, the treatment caused tumor and nodal remission. In the prediction of this therapy response, hematological and genetic parameters, such as NLR, P53, MLH1, and MSH2, play a predictive role.

摘要

背景/目的:本研究旨在确定一种预测性生物标志物,用于检测诊断为直肠癌并接受新辅助放化疗(nCRT)患者的治疗反应。

材料与方法

回顾性评估了37例接受nCRT患者的数据。采用免疫组织化学方法评估DNA错配修复(MMR)基因中的p53评分以及MLH1和MSH2的基因不稳定性。从计算机记录中获取中性粒细胞与白细胞比值(NLR)、癌胚抗原(CEA)和糖类抗原(CA)19-9值作为血液学参数。根据Ryan等人修改后的分级系统对nCRT后治疗反应的病理分析进行分类。结果:治疗前后NLR、CEA和CA19-9值的变化具有统计学意义(p<0.001和p=0.005)。检测到治疗后第5周CEA值下降对病理反应评分有接近显著的影响(p=0.075)。有任何残留的患者的p53突变评分高于完全缓解患者。总体而言,89.2%的患者表现为MMR阳性(稳定),10.8%的MMR阴性(不稳定)病例有肉眼可见残留。病理完全缓解的病例为MMR阳性。

结论

因此,在大多数接受nCRT治疗的患者中,治疗导致肿瘤和淋巴结缓解。在预测这种治疗反应时,NLR、P53、MLH1和MSH2等血液学和遗传学参数发挥着预测作用。

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