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人表皮生长因子受体2扩增型晚期直肠癌的精准治疗:一例报告

Precision treatment for human epidermal growth factor receptor 2-amplified advanced rectal cancer: A case report.

作者信息

Xiao Xia, Wang Qing-Wen, Zhou Zheng-Yang, Wang Lei-Sheng, Huang Pei

机构信息

Department of Oncology, Wuxi No. 2 People's Hospital, Jiangnan University Medical Center, Wuxi 214002, Jiangsu Province, China.

Wuxi Medical College, Jiangnan University, Wuxi 214122, Jiangsu Province, China.

出版信息

World J Gastrointest Oncol. 2025 Apr 15;17(4):102690. doi: 10.4251/wjgo.v17.i4.102690.

DOI:10.4251/wjgo.v17.i4.102690
PMID:40235909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11995321/
Abstract

BACKGROUND

Although targeted therapy provides survival benefits for patients with metastatic colorectal cancer, some patients develop resistance to these treatments. Human epidermal growth factor receptor 2 (HER2) is overexpressed in a subset of patients with colorectal cancer and has been established as a therapeutic target.

CASE SUMMARY

This case report describes a Chinese patient with HER2-amplified advanced rectal cancer who showed no response to chemotherapy and targeted therapies against epidermal growth factor receptor and vascular endothelial growth factor but achieved a remarkable response following treatment with immune checkpoint inhibitors (ICIs) in combination with pyrotinib. The combination of oxaliplatin and ICIs with pyrotinib demonstrates synergistic effects after late-stage disease progression.

CONCLUSION

ICIs and pyrotinib may be effective in treating HER2-amplified advanced rectal cancer. Chemotherapy following disease progression could enhance efficacy synergistically.

摘要

背景

尽管靶向治疗为转移性结直肠癌患者带来了生存益处,但一些患者会对这些治疗产生耐药性。人表皮生长因子受体2(HER2)在一部分结直肠癌患者中过度表达,并已被确立为治疗靶点。

病例摘要

本病例报告描述了一名HER2扩增的晚期直肠癌中国患者,该患者对化疗以及针对表皮生长因子受体和血管内皮生长因子的靶向治疗均无反应,但在接受免疫检查点抑制剂(ICI)联合吡咯替尼治疗后取得了显著疗效。奥沙利铂与ICI联合吡咯替尼在疾病晚期进展后显示出协同作用。

结论

ICI和吡咯替尼可能对治疗HER2扩增的晚期直肠癌有效。疾病进展后进行化疗可协同增强疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3c/11995321/34bd6ffa1376/102690-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3c/11995321/35ba46868378/102690-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3c/11995321/ee8333a4db2c/102690-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3c/11995321/34bd6ffa1376/102690-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3c/11995321/35ba46868378/102690-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3c/11995321/ee8333a4db2c/102690-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3c/11995321/34bd6ffa1376/102690-g003.jpg

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Pembrolizumab for previously treated, microsatellite instability-high/mismatch repair-deficient advanced colorectal cancer: final analysis of KEYNOTE-164.帕博利珠单抗治疗既往治疗、微卫星不稳定高/错配修复缺陷型晚期结直肠癌:KEYNOTE-164 的最终分析。
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Real-world survival of patients with advanced BRAF V600 mutated melanoma treated with front-line BRAF/MEK inhibitors, anti-PD-1 antibodies, or nivolumab/ipilimumab.一线 BRAF/MEK 抑制剂、抗 PD-1 抗体或纳武利尤单抗/伊匹木单抗治疗晚期 BRAF V600 突变黑色素瘤患者的真实世界生存情况。
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HER2-targeted therapy should be shifted towards an earlier line for patients with anti-EGFR-therapy naïve, -amplified metastatic colorectal cancer.对于未接受过抗表皮生长因子受体(EGFR)治疗、存在EGFR扩增的转移性结直肠癌患者,人表皮生长因子受体2(HER2)靶向治疗应提前至更靠前的治疗线序。
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