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转移性结肠癌中与新辅助化疗敏感性相关的基因突变:一例报告及文献综述

Genetic mutations associated with sensitivity to neoadjuvant chemotherapy in metastatic colon cancer: A case report and review of literature.

作者信息

Zhao Long, Wang Quan, Zhao Shi-Dong, Zhou Jing, Jiang Ke-Wei, Ye Ying-Jiang, Wang Shan, Shen Zhan-Long

机构信息

Department of Gastroenterological Surgery, Laboratory of Surgical Oncology, Beijing Key Laboratory of Colorectal Cancer Diagnosis and Treatment Research, Peking University People's Hospital, Beijing 100044, China.

出版信息

World J Clin Cases. 2021 Aug 26;9(24):7099-7109. doi: 10.12998/wjcc.v9.i24.7099.

Abstract

BACKGROUND

Colorectal liver metastases (CLM) occur in 15%-30% of patients with colorectal cancer (CRC). Advancements in next generation sequencing (NGS) can provide more precise prognoses for cancer patients and help guide clinical treatment. However, the genetic variants that predict high sensitivity to neoadjuvant chemotherapy remain unclear, especially in patients with CLM. The aim of this study was to identify the relevant genetic variants in a single CLM patient and to summarize the current evidence on mutations and single nucleotide polymorphisms (SNPs) that objectively predict sensitivity to neoadjuvant chemotherapy.

CASE SUMMARY

A 76-year-old male patient, who was diagnosed as stage IV colon cancer with liver metastases, was found to have mutations. He showed a good therapeutic response to 12 courses of oxaliplatin regimens combined with Bevacizumab. Genetic analysis of the patient identified 5 genes with 7 detected SNPs that may be related to a better response to chemotherapy drugs. In addition, a critical literature review was performed based on a standardized appraisal form after selecting the articles. Ultimately, 21 eligible studies were appraised to assess the association between gene mutations and good prognosis. Mutations in and were identified as being associated with a poor response to chemotherapy drugs, whereas mutations of and were associated with longer overall survival.

CONCLUSION

NGS can identify precise predictors of response to neoadjuvant chemotherapy, leading to improved outcomes for CRC patients.

摘要

背景

结直肠癌肝转移(CLM)发生于15%-30%的结直肠癌(CRC)患者中。下一代测序(NGS)技术的进步可为癌症患者提供更精确的预后评估,并有助于指导临床治疗。然而,预测对新辅助化疗高敏感性的基因变异仍不明确,尤其是在CLM患者中。本研究的目的是在一名CLM患者中鉴定相关基因变异,并总结目前关于客观预测新辅助化疗敏感性的突变和单核苷酸多态性(SNP)的证据。

病例摘要

一名76岁男性患者,被诊断为伴有肝转移的IV期结肠癌,发现存在 突变。他对12个疗程的奥沙利铂方案联合贝伐单抗显示出良好的治疗反应。对该患者的基因分析确定了5个基因,检测到7个可能与化疗药物更好反应相关的SNP。此外,在选择文章后,根据标准化评估表进行了关键文献综述。最终,对21项符合条件的研究进行评估,以评估基因突变与良好预后之间的关联。 和 中的突变被确定与化疗药物反应不佳有关,而 和 的突变与更长的总生存期有关。

结论

NGS可以识别新辅助化疗反应的精确预测指标,从而改善CRC患者的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ea/8409210/69dc41a8d22c/WJCC-9-7099-g001.jpg

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