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采用核心针活检标本上清液的肺腺癌液体活检检测。

Liquid biopsy assay for pulmonary adenocarcinoma using supernatants from core-needle biopsy specimens.

机构信息

Department of Minimally Invasive Tumor Therapies Center, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medicine Sciences, Beijing, China.

Graduate School of Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.

出版信息

Thorac Cancer. 2022 Jun;13(12):1822-1826. doi: 10.1111/1759-7714.14461. Epub 2022 May 16.

Abstract

BACKGROUND

Genomic testing is the cornerstone of the treatment of patients with non-small-cell lung cancer. However, comprehensive molecular testing of small specimens may be inadequate due to limited tissue. Liquid biopsy has emerged as a new method of genotyping. In this study, we evaluate the feasibility of using supernatants from core needle biopsy samples of lung adenocarcinoma for genomic testing.

METHODS

Core needle biopsy specimens and their supernatants were collected from patients (n = 48) with lung adenocarcinoma. Genomic testing results of the supernatant samples were compared with results derived from paired tissue samples from the same patient.

RESULT

All 48 supernatant samples yield adequate cell-free DNA, but the concentration of cell-free RNA did not meet the criteria for analysis. The concordance rate between the genomic testing results of supernatants and the corresponding tissue samples was 95.8% (kappa = 0.899). The coincidence rate of detectable mutations at the DNA level in the supernatants was up to 100%.

CONCLUSION

Core needle biopsy supernatants can provide a valuable specimen source for genotyping pulmonary adenocarcinoma. However, the method of preserving and extracting RNA from supernatant specimens needs further improvement.

摘要

背景

基因组检测是治疗非小细胞肺癌患者的基石。然而,由于组织有限,对小标本进行全面的分子检测可能不够。液体活检已成为一种新的基因分型方法。本研究评估了使用肺腺癌的核心针活检样本上清液进行基因组检测的可行性。

方法

收集 48 例肺腺癌患者的核心针活检标本及其上清液。将上清液样本的基因组检测结果与来自同一患者的配对组织样本的检测结果进行比较。

结果

所有 48 个上清液样本均产生足够的游离 DNA,但游离 RNA 的浓度不符合分析标准。上清液与相应组织样本的基因组检测结果之间的一致性率为 95.8%(kappa=0.899)。上清液中 DNA 水平可检测突变的符合率高达 100%。

结论

核心针活检上清液可为肺腺癌的基因分型提供有价值的标本来源。然而,需要进一步改进从上清液标本中保存和提取 RNA 的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2808/9200882/ac9202e47263/TCA-13-1822-g001.jpg

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