• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

中国晚期肺腺癌伴间变性淋巴瘤激酶重排患者的临床病理特征和治疗反应。

Clinicopathological Features and Therapeutic Responses of Chinese Patients with Advanced Lung Adenocarcinoma Harboring an Anaplastic Lymphoma Kinase Rearrangement.

出版信息

Oncol Res Treat. 2017;40(1-2):27-33. doi: 10.1159/000454715. Epub 2017 Jan 16.

DOI:10.1159/000454715
PMID:28118634
Abstract

BACKGROUND

Presence of anaplastic lymphoma kinase (ALK) rearrangement is an indication for crizotinib in the treatment of patients with advanced or metastatic lung adenocarcinoma. Here, we sought to elucidate the association between clinicopathological features and ALK rearrangement status in Chinese patients with advanced lung adenocarcinoma harboring an ALK rearrangement.

PATIENTS AND METHODS

ALK rearrangement status was determined using immunohistochemistry (IHC) in tumor tissues from 120 patients with advanced lung adenocarcinoma, and further assessed by fluorescence in situ hybridization (FISH) assay. The associations between ALK rearrangement status and clinicopathological features were analyzed.

RESULTS

According to IHC testing, the ALK-positive rate among the advanced lung adenocarcinoma patients was 6.67% (8/120). FISH validation found 5 patients with ALK rearrangement among the 8 IHC-positive cases. No significant difference was observed regarding age, sex, or smoking status between FISH-positive and -negative patients (p > 0.05). None of the 5 FISH-positive patients benefited from first-line chemotherapy.

CONCLUSION

IHC can be used as a reliable method for ALK rearrangement screening in patients with lung adenocarcinoma, but further FISH validation is imperative. Presence of ALK rearrangement predicts a more aggressive biological behavior of the tumor and might be indicative of poor response to chemotherapy.

摘要

背景

存在间变性淋巴瘤激酶(ALK)重排是克唑替尼治疗晚期或转移性肺腺癌患者的指征。在这里,我们试图阐明在中国晚期肺腺癌患者中,ALK 重排与临床病理特征之间的关联,这些患者携带 ALK 重排。

患者和方法

使用免疫组织化学(IHC)检测 120 例晚期肺腺癌患者肿瘤组织中的 ALK 重排状态,并通过荧光原位杂交(FISH)检测进一步评估。分析 ALK 重排状态与临床病理特征之间的关联。

结果

根据 IHC 检测,晚期肺腺癌患者中 ALK 阳性率为 6.67%(8/120)。FISH 验证发现 8 例 IHC 阳性病例中有 5 例存在 ALK 重排。FISH 阳性和阴性患者在年龄、性别或吸烟状况方面无显著差异(p>0.05)。5 例 FISH 阳性患者均未从一线化疗中获益。

结论

IHC 可作为肺腺癌患者 ALK 重排筛查的可靠方法,但仍需进一步的 FISH 验证。ALK 重排的存在预示着肿瘤具有更具侵袭性的生物学行为,可能提示对化疗反应不佳。

相似文献

1
Clinicopathological Features and Therapeutic Responses of Chinese Patients with Advanced Lung Adenocarcinoma Harboring an Anaplastic Lymphoma Kinase Rearrangement.中国晚期肺腺癌伴间变性淋巴瘤激酶重排患者的临床病理特征和治疗反应。
Oncol Res Treat. 2017;40(1-2):27-33. doi: 10.1159/000454715. Epub 2017 Jan 16.
2
Responses to crizotinib in patients with ALK-positive lung adenocarcinoma who tested immunohistochemistry (IHC)-positive and fluorescence in situ hybridization (FISH)-negative.对免疫组织化学(IHC)呈阳性且荧光原位杂交(FISH)呈阴性的ALK阳性肺腺癌患者使用克唑替尼的反应。
Oncotarget. 2016 Sep 27;7(39):64410-64420. doi: 10.18632/oncotarget.10560.
3
Effectiveness of crizotinib in a patient with ALK IHC-positive/FISH-negative metastatic lung adenocarcinoma.克唑替尼在一名ALK免疫组化阳性/荧光原位杂交阴性转移性肺腺癌患者中的疗效。
Lung Cancer. 2016 Aug;98:118-121. doi: 10.1016/j.lungcan.2016.06.001. Epub 2016 Jun 3.
4
An Anaplastic Lymphoma Kinase Immunohistochemistry-Negative but Fluorescence In Situ Hybridization-Positive Lung Adenocarcinoma Is Resistant to Crizotinib.间变性淋巴瘤激酶免疫组化阴性但荧光原位杂交阳性的肺腺癌对克唑替尼耐药。
J Thorac Oncol. 2016 Dec;11(12):2248-2252. doi: 10.1016/j.jtho.2016.08.139. Epub 2016 Sep 6.
5
ALK FISH patterns and the detection of ALK fusions by next generation sequencing in lung adenocarcinoma.肺腺癌中ALK荧光原位杂交(FISH)模式及通过下一代测序检测ALK融合
Oncotarget. 2016 Dec 13;7(50):82943-82952. doi: 10.18632/oncotarget.12705.
6
French multicentric validation of ALK rearrangement diagnostic in 547 lung adenocarcinomas.547 例肺腺癌中 ALK 重排诊断的法国多中心验证。
Eur Respir J. 2015 Jul;46(1):207-18. doi: 10.1183/09031936.00119914. Epub 2015 Apr 30.
7
ALK-rearranged pulmonary adenocarcinoma in Thai Patients: From diagnosis to treatment efficacy.泰国患者的ALK重排肺腺癌:从诊断到治疗效果
World J Surg Oncol. 2016 May 3;14:139. doi: 10.1186/s12957-016-0893-6.
8
Discrepancies between FISH and immunohistochemistry for assessment of the ALK status are associated with ALK 'borderline'-positive rearrangements or a high copy number: a potential major issue for anti-ALK therapeutic strategies.荧光原位杂交(Fish)和免疫组织化学(IHC)在评估 ALK 状态方面的差异与 ALK“临界阳性”重排或高拷贝数有关:这可能是针对 ALK 的治疗策略的一个主要问题。
Ann Oncol. 2015 Jan;26(1):238-244. doi: 10.1093/annonc/mdu484. Epub 2014 Oct 24.
9
Combinational Analysis of FISH and Immunohistochemistry Reveals Rare Genomic Events in ALK Fusion Patterns in NSCLC that Responds to Crizotinib Treatment.荧光原位杂交(FISH)和免疫组织化学组合分析揭示了 NSCLC 中 ALK 融合模式的罕见基因组事件,这些事件对克唑替尼治疗有反应。
J Thorac Oncol. 2017 Jan;12(1):94-101. doi: 10.1016/j.jtho.2016.08.145. Epub 2016 Sep 8.
10
Is there a progression-free survival benefit of first-line crizotinib versus standard chemotherapy and second-line crizotinib in ALK-positive advanced lung adenocarcinoma? A retrospective study of Chinese patients.在ALK阳性的晚期肺腺癌患者中,一线克唑替尼相对于标准化疗以及二线克唑替尼在无进展生存期方面是否具有获益?一项针对中国患者的回顾性研究。
Cancer Med. 2016 Jun;5(6):1013-21. doi: 10.1002/cam4.659. Epub 2016 Feb 16.