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KRAS-Mutant Non-Small Cell Lung Cancer: An Emerging Promisingly Treatable Subgroup.

作者信息

Xie Mingying, Xu Xiaoling, Fan Yun

机构信息

Department of Medical Oncology, The Second Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou, China.

Department of Medical Oncology, The Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Hangzhou, China.

出版信息

Front Oncol. 2021 May 3;11:672612. doi: 10.3389/fonc.2021.672612. eCollection 2021.


DOI:10.3389/fonc.2021.672612
PMID:34012925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8126715/
Abstract

Lung cancer, the leading cause of cancer-related deaths worldwide, can be classified into small cell lung cancer and non-small cell lung cancer (NSCLC). NSCLC is the most common histological type, accounting for 85% of all lung cancers. Kirsten rat sarcoma viral oncogene (KRAS) mutations, common in NSCLC, are associated with poor prognosis, likely due to poor responses to most systemic therapies and lack of targeted drugs. The latest published clinical trial data on new small-molecule KRAS G12C inhibitors, AMG510 and MRTX849, indicate that these molecules may potentially help treat KRAS-mutant NSCLC. Simultaneously, within the immuno-therapeutic process, immune efficacy has been observed in those patients who have mutations. In this article, the pathogenesis, treatment status, progress of immunotherapy, and targeted therapy of KRAS-mutant NSCLC are reviewed.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a15/8126715/3e28db61840e/fonc-11-672612-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a15/8126715/3e28db61840e/fonc-11-672612-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a15/8126715/3e28db61840e/fonc-11-672612-g001.jpg

相似文献

[1]
KRAS-Mutant Non-Small Cell Lung Cancer: An Emerging Promisingly Treatable Subgroup.

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[2]
[Current status and outlook of medical treatment for -mutated non-small cell lung cancer].

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[3]
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[4]
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[5]
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[6]
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[7]
Clinical outcomes of -mutant non-small cell lung cancer under untargeted therapeutic regimes in the real world: a retrospective observational study.

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[8]
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[9]
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[10]
Inside the cracked kernel: establishing the molecular basis of AMG510 and MRTX849 in destabilising KRASG12C mutant switch I and II in cancer treatment.

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[4]
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[5]
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[6]
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[8]
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本文引用的文献

[1]
Pretreatment neutrophil-to-lymphocyte ratio and mutational burden as biomarkers of tumor response to immune checkpoint inhibitors.

Nat Commun. 2021-2-1

[2]
First-line nivolumab plus ipilimumab combined with two cycles of chemotherapy in patients with non-small-cell lung cancer (CheckMate 9LA): an international, randomised, open-label, phase 3 trial.

Lancet Oncol. 2021-2

[3]
Targeting -Mutant Non-Small-Cell Lung Cancer: One Mutation at a Time, With a Focus on Mutations.

J Clin Oncol. 2020-12-10

[4]
KRAS Inhibition with Sotorasib in Advanced Solid Tumors.

N Engl J Med. 2020-9-20

[5]
KRAS: From undruggable to a druggable Cancer Target.

Cancer Treat Rev. 2020-7-15

[6]
Current therapy of KRAS-mutant lung cancer.

Cancer Metastasis Rev. 2020-12

[7]
RAS-targeted therapies: is the undruggable drugged?

Nat Rev Drug Discov. 2020-6-11

[8]
A Deregulated HOX Gene Axis Confers an Epigenetic Vulnerability in KRAS-Mutant Lung Cancers.

Cancer Cell. 2020-4-2

[9]
KRAS as a druggable target in NSCLC: Rising like a phoenix after decades of development failures.

Cancer Treat Rev. 2020-2-7

[10]
Tumor mutational load, CD8 T cells, expression of PD-L1 and HLA class I to guide immunotherapy decisions in NSCLC patients.

Cancer Immunol Immunother. 2020-2-12

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