舒伐他尼治疗肺腺癌 HER2 20 外显子插入的首个病例报告。

IF 1.8 4区 医学 Q3 ONCOLOGY Anti-Cancer Drugs Pub Date : 2024-09-01 Epub Date: 2024-06-26 DOI:10.1097/CAD.0000000000001628
Tao Luan, Xinqing Lin, Xiaohong Xie, Gang Yang, Shuaiying Wang, Jianqing Hao, Chengzhi Zhou
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引用次数: 0

摘要

人表皮生长因子受体 2(HER2)是一种跨膜糖蛋白受体,具有细胞内酪氨酸激酶活性。它通常被认为是预后不良的标志物。小分子酪氨酸激酶抑制剂(TKIs)等靶向疗法对HER2突变的晚期非小细胞肺癌(NSCLC)疗效有限。在 2023 年美国国家综合癌症网络(NSCLC National Comprehensive Cancer Network)指南中,推荐使用抗体药物共轭物曲妥珠单抗(trastuzumab emtansine)治疗 HER2 突变肺癌。因此,有必要为HER2突变型NSCLC患者探索其他治疗方案。在我们对一名曾接受多种表皮生长因子受体(EGFR)-TKI治疗失败的HER2外显子20插入肺腺癌患者的研究中,我们发现舒伐他尼可以稳定患者的病情,实现87天的无进展生存期。这是一项新发现,可为TKI治疗失败的HER2外显子20插入患者提供新的治疗方案。
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First case report of sunvozertinib for the treatment of HER2 exon 20 insertion in lung adenocarcinoma.

Human epidermal growth factor receptor 2 (HER2) is a transmembrane glycoprotein receptor with intracellular tyrosine kinase activity. It is generally considered as a poor prognostic marker. Targeted therapies, such as small molecule tyrosine kinase inhibitors (TKIs), showed limited efficacy in HER2-mutant advanced nonsmall cell lung cancer (NSCLC). In the 2023 National Comprehensive Cancer Network guidelines for NSCLC, antibody-drug conjugate trastuzumab emtansine is recommended for the treatment of HER2-mutant lung cancer. However, this medication is currently not approved in certain regions. So it is necessary to explore alternative treatment options for HER2-mutant NSCLC patients. In our study of a patient with HER2 exon 20 insertion lung adenocarcinoma who had previously failed multiple epidermal growth factor receptor (EGFR)-TKI treatments, we discovered that sunvozertinib could stabilize the patient's condition, achieving a progression-free survival of 87 days. This is a novel finding that may provide new treatment options for HER2 exon 20 insertion patients who have failed TKI therapy.

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来源期刊
Anti-Cancer Drugs
Anti-Cancer Drugs 医学-药学
CiteScore
3.80
自引率
0.00%
发文量
244
审稿时长
3 months
期刊介绍: Anti-Cancer Drugs reports both clinical and experimental results related to anti-cancer drugs, and welcomes contributions on anti-cancer drug design, drug delivery, pharmacology, hormonal and biological modalities and chemotherapy evaluation. An internationally refereed journal devoted to the fast publication of innovative investigations on therapeutic agents against cancer, Anti-Cancer Drugs aims to stimulate and report research on both toxic and non-toxic anti-cancer agents. Consequently, the scope on the journal will cover both conventional cytotoxic chemotherapy and hormonal or biological response modalities such as interleukins and immunotherapy. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool.
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