Comprehensive analysis of NGS and ARMS-PCR for detecting EGFR mutations based on 4467 cases of NSCLC patients
Adult
Male
0301 basic medicine
China
Lung Neoplasms
DNA Mutational Analysis
Polymerase Chain Reaction
Cohort Studies
03 medical and health sciences
0302 clinical medicine
Predictive Value of Tests
Carcinoma, Non-Small-Cell Lung
Humans
Genetic Testing
Aged
Aged, 80 and over
High-Throughput Nucleotide Sequencing
Middle Aged
3. Good health
ErbB Receptors
Mutation
Female
Original Article – Cancer Research
DOI:
10.1007/s00432-021-03818-w
Publication Date:
2021-10-24T16:02:50Z
AUTHORS (11)
ABSTRACT
By comparing the detection rate and type of targeted gene mutations in non-small cell lung cancer (NSCLC) between amplification refractory mutation system PCR (ARMS-PCR) next-generation sequencing (NGS), characteristics application advantages are explained, providing a basis for clinicians to effectively select corresponding methods.The cases genes were selected from First Affiliated Hospital Chongqing Medical University January 2016 October 2020. A sample 4467 was selected, they diagnosed with NSCLC by Pathological biopsy. Sample sources include surgical resection, bronchoscope biopsy, metastatic blood, sputum, cytology pleural effusion. Among them, 3665 detected ARMS-PCR technique, 802 NGS technology. The techniques EGFR (including exon 18, 19, 20, 21 so on) different samples compared, respectively.The total 47.6% while 42.4% which indicated that there significant difference two methods detecting (P < 0.001). In exons, is various. 19 evidently higher than detection, exons 20 statistically significantly lower detection. Moreover, multiple 16.3% much 2.7% different.It showed could direct drug use resistant patients. However, some rare loci be but importance directed meaning still unknown number too. Further research on new biomarkers technique needed early diagnosis, directing assessing therapy prognosis.
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