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作为非小细胞肺癌中具有**某种突变**的克唑替尼耐药的一种获得性潜在机制的**该突变**。 备注:原文中两个mutation指代不明,我按照字面进行了翻译,翻译出来的句子读起来不通顺,建议你检查下原文是否准确完整。

Mutation of as an Acquired Potential Mechanism of Crizotinib Resistance in NSCLC with Mutation.

作者信息

Zhu Jinlian, Chen Jie, Liu Wei, Zhang Junling, Gu Yulan

机构信息

Department of Oncology, Affiliated Changshu Hospital of Nantong University, Changshu, Jiangsu Province, People's Republic of China.

Medical Department, 3D Medicines Inc, Shanghai, People's Republic of China.

出版信息

Lung Cancer (Auckl). 2024 Aug 27;15:123-128. doi: 10.2147/LCTT.S467584. eCollection 2024.

Abstract

Mesenchymal-epithelial transition () gene has been identified as a promising target for treatments. However, different sites of the mutation show different effects to MET inhibition. Here, we reported a non-small cell lung cancer (NSCLC) patient harboring mutation who achieved a durable partial response to crizotinib with a PFS of 22.4 months. Furthermore, we report for the first time the identification of as a possible mechanism of acquired resistance to crizotinib in a patient with mutation during disease progression.

摘要

间充质-上皮转化()基因已被确定为一种有前景的治疗靶点。然而,该突变的不同位点对MET抑制表现出不同的效果。在此,我们报告了一名携带该突变的非小细胞肺癌(NSCLC)患者,其对克唑替尼取得了持久的部分缓解,无进展生存期为22.4个月。此外,我们首次报告了在一名携带该突变的患者疾病进展过程中,发现该情况是对克唑替尼获得性耐药的一种可能机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3100/11365520/9269f5893244/LCTT-15-123-g0001.jpg

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