Suppr超能文献

一线克唑替尼治疗在一例 IV 期肺腺癌患者中的新型 SEC31A-间变性淋巴瘤激酶融合:病例报告及文献复习。

First-line crizotinib therapy is effective for a novel SEC31A-anaplastic lymphoma kinase fusion in a patient with stage IV lung adenocarcinoma: a case report and literature reviews.

机构信息

Department of Radiology, The First People's Hospital of Yunnan Province/Affiliated Hospital of Kunming University of Science and Technology and Departments of.

Respiratory and Critical Care Medicine.

出版信息

Anticancer Drugs. 2023 Feb 1;34(2):294-301. doi: 10.1097/CAD.0000000000001408. Epub 2022 Nov 16.

Abstract

Anaplastic lymphoma kinase (ALK) fusion was found in 3-7% of all patients with nonsmall cell lung cancer. The efficacy of ALK-tyrosine kinase inhibitor (ALK-TKI) in EML4-ALK has been extensively studied, whereas little evidence is available on its efficacy in rare ALK fusions. Here, we report the performance of crizotinib in a 50-year-old male lung adenocarcinoma patient with a novel rare SEC31A-ALK fusion. Computed tomography (CT) scan revealed multiple patchy high-density shadows in both lungs. The larger ones are located near the spine in the right lung lower lobe (55 × 34 mm) and the left hilar region (45 × 26 mm), with multiple enlarged mediastinal and axillary lymph nodes. Biopsy by bronchoscopy revealed invasive adenocarcinoma. The pathological stage of T4N3M1b (clinical stage: IVA) was confirmed. Next-generation sequencing revealed SEC31A: exon20ALK: exon20 fusion, ABCB1 amplification, FGF19 amplification, DAXX p.S213L, MUTYH p.R19*(germline mutation and pathogenic) with tumor mutational burden at 3.2 mutations/Mb, microsatellite stable, proficient mismatch repair and PD-L1 positive [immunohistochemistry, tumor proportion score(TPS) 1-49% (TPS = 25%)]. Based on these findings, crizotinib was recommended for the first-line treatment at 250 mg twice daily. The first CT assessment after 2-month therapy showed partial response (PR) for the two larger lesions, multiple shadows and nodules in both lungs and the mediastinal and axillary lymph nodes. Crizotinib at 250 mg twice a day was applied in the following 9 months. Assessment at every 3 months (up to 1-year after diagnosis) showed further absorption for all lesions (continuous PR). We reported a novel rare ALK fusion SEC31A: EXON20ALK: exon20 and showed the effectiveness of crizotinib against the fusion. This study provided strong evidence for the efficacy of ALK-TKI for rare ALK fusion.

摘要

间变性淋巴瘤激酶(ALK)融合在所有非小细胞肺癌患者中占 3-7%。EML4-ALK 中的 ALK 酪氨酸激酶抑制剂(ALK-TKI)的疗效已得到广泛研究,而关于其在罕见 ALK 融合中的疗效的证据很少。在这里,我们报告了克唑替尼在一位 50 岁男性肺腺癌患者中的表现,该患者存在新型罕见 SEC31A-ALK 融合。计算机断层扫描(CT)显示双肺多处斑片状高密度影。较大的病变位于右肺下叶靠近脊柱处(55×34mm)和左肺门区(45×26mm),伴多个纵隔和腋窝淋巴结肿大。支气管镜活检显示浸润性腺癌。病理分期为 T4N3M1b(临床分期:IVA 期)。下一代测序显示 SEC31A:exon20ALK:exon20 融合、ABCB1 扩增、FGF19 扩增、DAXX p.S213L、MUTYH p.R19*(种系突变和致病性),肿瘤突变负荷为 3.2 个突变/Mb,微卫星稳定,错配修复功能完整,PD-L1 阳性[免疫组化,肿瘤比例评分(TPS)1-49%(TPS=25%)]。基于这些发现,建议推荐克唑替尼作为一线治疗药物,剂量为 250mg,每日两次。治疗 2 个月后的首次 CT 评估显示两个较大病变、双肺内多个阴影和结节以及纵隔和腋窝淋巴结有部分缓解(PR)。接下来的 9 个月内,每日两次应用克唑替尼(剂量为 250mg)。每 3 个月(诊断后 1 年)进行一次评估,结果显示所有病变进一步吸收(持续 PR)。我们报道了一种新型罕见的 ALK 融合 SEC31A:exon20ALK:exon20,并显示了克唑替尼对该融合的有效性。本研究为罕见 ALK 融合的 ALK-TKI 疗效提供了有力证据。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验