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携带罕见delE709_T710insD突变的晚期非小细胞肺癌对达可替尼的反应:一例报告

Response to dacomitinib in advanced non-small-cell lung cancer harboring the rare delE709_T710insD mutation: A case report.

作者信息

Xu Fei, Xia Meng-Ling, Pan Hui-Yun, Pan Jiong-Wei, Shen Yi-Hong

机构信息

Department of Respiratory Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310000, Zhejiang Province, China.

Department of Day Care Ward, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310000, Zhejiang Province, China.

出版信息

World J Clin Cases. 2022 Jun 16;10(17):5916-5922. doi: 10.12998/wjcc.v10.i17.5916.

Abstract

BACKGROUND

Tyrosine kinase inhibitors (TKI) have been the standard first-line therapy for advanced non-small cell lung cancer (NSCLC) of epidermal growth factor receptor () sensitive mutations. Uncommon mutations are increasingly reported with the development of next-generation sequencing. However, their sensitivity to TKIs is variable with limited clinical evidence.

CASE SUMMARY

Here, we report a patient with the rare delE709_T710insD mutation, who showed the favorable efficacy of dacomitinib and achieved a partial response with a progression-free survival of 7.0 mo.

CONCLUSION

To our knowledge, this is the first report displaying the clinical efficacy of dacomitinib for patients with delE709_T710insD, which may help to provide alternatives in non-classical variant NSCLC patients. Further studies are warranted to make the optimal choice of -TKI for rare mutations.

摘要

背景

酪氨酸激酶抑制剂(TKI)一直是表皮生长因子受体()敏感突变的晚期非小细胞肺癌(NSCLC)的标准一线治疗方法。随着下一代测序技术的发展,越来越多不常见的突变被报道。然而,它们对TKI的敏感性各不相同,临床证据有限。

病例总结

在此,我们报告一名患有罕见的delE709_T710insD突变的患者,该患者显示出达可替尼的良好疗效,并实现了部分缓解,无进展生存期为7.0个月。

结论

据我们所知,这是第一份展示达可替尼对delE709_T710insD患者临床疗效的报告,这可能有助于为非经典变异NSCLC患者提供替代方案。有必要进行进一步研究,以针对罕见突变做出-TKI的最佳选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a1f/9258371/15e430b1493b/WJCC-10-5916-g001.jpg

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