Abstract | BACKGROUND: METHODS: Pre- and in-treatment blood samples were collected from 14 patients with lung cancer receiving chemotherapy. Based on next-generation sequencing technology, we constructed a unique molecular identifier (UMI) library and performed targeted deep sequencing of 72 genes (15 000×). We used dVAF to evaluate the change level and trend of variant allele frequency (VAF). RESULTS: We identified MUC16, KMT2D, AMER1, and NTRK1 as the most-frequently mutated genes in ctDNA associated with lung cancer. Furthermore, we showed that the change trend of dVAF in patients with lung cancer undergoing chemotherapy was closely related to the changes in both tumor volume and tumor biomarkers, including CEA, CA125, NSE, and CK ( Cytokeratin). Moreover, the ctDNA analysis revealed disease progression of SCLC patients earlier than did computed tomography. CONCLUSIONS: The dynamic detection of plasma ctDNA VAF has the potential value as a biomarker for evaluating the efficacy of chemotherapy in patients with SCLC and advanced NSCLC, and may predict the progression of lung cancer patients earlier than radiography.
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Authors | Min Zhang, Chao Huang, Huan Zhou, Dan Liu, Runze Chen, Xiuhua Li, Ye Cheng, Bing Gao, Jun Chen |
Journal | Thoracic cancer
(Thorac Cancer)
Vol. 13
Issue 1
Pg. 95-106
(01 2022)
ISSN: 1759-7714 [Electronic] Singapore |
PMID | 34791810
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2021 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. |
Chemical References |
- Biomarkers, Tumor
- Circulating Tumor DNA
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Topics |
- Aged
- Biomarkers, Tumor
(genetics)
- Circulating Tumor DNA
(genetics)
- Disease Progression
- Drug Therapy
(methods)
- Female
- High-Throughput Nucleotide Sequencing
- Humans
- Lung Neoplasms
(drug therapy, genetics, pathology)
- Male
- Middle Aged
- Mutation
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