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8号染色体非整倍体和循环肿瘤细胞突变可预测局部晚期直肠癌治疗中的病理完全缓解。

Aneuploidy of chromosome 8 and mutation of circulating tumor cells predict pathologic complete response in the treatment of locally advanced rectal cancer.

作者信息

Wan Jue-Feng, Li Xue-Qin, Zhang Jing, Yang Li-Feng, Zhu Ji, Li Gui-Chao, Liang Li-Ping, Shen Li-Jun, Zhang Hui, Li Jing, Zhang Yi-Tong, Chen Chang-Yue, Zhang Zhen

机构信息

Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, P.R. China.

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, P.R. China.

出版信息

Oncol Lett. 2018 Aug;16(2):1863-1868. doi: 10.3892/ol.2018.8831. Epub 2018 May 30.

Abstract

Identifying patients who may or may not achieve pathologic complete response (pathCR) allows for treatment with alternative approaches in the preoperative setting. The aim of the current study was to investigate whether aneuploidy of chromosome 8 and mutations of circulating tumor cells (CTCs) could predict the response of patients with rectal cancer to preoperative chemoradiotherapy. A total of 33 patients with locally advanced rectal cancer (cT3-T4 and/or cN+) treated with neoadjuvant chemoradiotherapy between September 2014 and March 2015 were recruited. Blood samples were collected from 33 patients with pre-chemoradiotherapy rectal cancer. It was demonstrated that ≥5 copies of chromosome 8 was associated with pathCR (univariate logistic regression, P=0.042). Of the 6 patients whose CTCs had <5 copies of chromosome 8, 3 achieved pathCR (3/6, 50%), and of the 27 patients whose CTCs had ≥5 copies of chromosome 8 obtained 3 pathCR (3/27, 11.1%; Chi-square test, P=0.0255). Of the 33 patients with mutations assessed, 8 significant nonsynonymous mutations in CTCs were identified as associated with pathCR (Chi-square test, P-values range, 0.0004-0.0298; mutations in ARID1A, HDAC1, APC, ERBB3, TP53, AMER1 and AR). These results suggest that ≥5 copies of chromosome 8 and 8 nonsynonymous mutations in ARID1A, HDAC1, APC, ERBB3, TP53, AMER1 AR in CTCs were associated with pathCR. This conclusion should be validated further in larger prospective studies and the long-term follow-up survival data of this study will also be reported in the future.

摘要

识别可能达到或未达到病理完全缓解(pathCR)的患者,有助于在术前阶段采用其他治疗方法。本研究的目的是调查8号染色体非整倍体和循环肿瘤细胞(CTC)突变是否能够预测直肠癌患者对术前放化疗的反应。2014年9月至2015年3月期间,共有33例接受新辅助放化疗的局部晚期直肠癌患者(cT3-T4和/或cN+)入组。采集了33例术前直肠癌患者的血样。结果表明,8号染色体≥5条拷贝与pathCR相关(单因素逻辑回归,P=0.042)。在6例CTC中8号染色体拷贝数<5条的患者中,3例实现了pathCR(3/6,50%);在27例CTC中8号染色体拷贝数≥5条的患者中,有3例实现了pathCR(3/27,11.1%;卡方检验,P=0.0255)。在评估的33例有突变的患者中,发现CTC中的8个显著非同义突变与pathCR相关(卡方检验,P值范围为0.0004-0.0298;ARID1A、HDAC1、APC、ERBB3、TP53、AMER1和AR中的突变)。这些结果表明,CTC中8号染色体≥5条拷贝以及ARID1A、HDAC1、APC、ERBB3、TP53、AMER1和AR中的8个非同义突变与pathCR相关。这一结论应在更大规模的前瞻性研究中进一步验证,本研究的长期随访生存数据也将在未来报告。

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SNES: single nucleus exome sequencing.SNES:单细胞核外显子组测序。
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