scholarly journals The diagnostic accuracy of digital PCR, ARMS and NGS for detecting KRAS mutation in cell-free DNA of patients with colorectal cancer: A systematic review and meta-analysis

PLoS ONE ◽  
2021 ◽  
Vol 16 (3) ◽  
pp. e0248775
Author(s):  
Peng Ye ◽  
Peiling Cai ◽  
Jing Xie ◽  
Yuanyuan Wei

Introduction Before anti-EGFR therapy is given to patients with colorectal cancer, it is required to determine KRAS mutation status in tumor. When tumor tissue is not available, cell-free DNA (liquid biopsy) is commonly used as an alternative. Due to the low abundance of tumor-derived DNA in cell-free DNA samples, methods with high sensitivity were preferred, including digital polymerase chain reaction, amplification refractory mutation system and next-generation sequencing. The aim of this systemic review and meta-analysis was to investigate the accuracy of those methods in detecting KRAS mutation in cell-free DNA sample from patients with colorectal cancer. Methods Literature search was performed in Pubmed, Embase, and Cochrane Library. After removing duplicates from the 170 publications found by literature search, eligible studies were identified using pre-defined criteria. Quality of the publications and relevant data were assessed and extracted thereafter. Meta-DiSc and STATA softwares were used to pool the accuracy parameters from the extracted data. Results A total of 33 eligible studies were identified for this systemic review and meta-analysis. After pooling, the overall sensitivity, specificity, and diagnostic odds ratio were 0.77 (95%CI: 0.74–0.79), 0.87 (95%CI: 0.85–0.89), and 23.96 (95%CI: 13.72–41.84), respectively. The overall positive and negative likelihood ratios were 5.55 (95%CI: 3.76–8.19) and 0.29 (95%CI: 0.21–0.38), respectively. Area under curve of the summarized ROC curve was 0.8992. Conclusion Digital polymerase chain reaction, amplification refractory mutation system, and next-generation sequencing had overall high accuracy in detecting KRAS mutation in cell-free DNA sample. Large prospective randomized clinical trials are needed to further convince the accuracy and usefulness of KRAS mutation detection using cfDNA/liquid biopsy samples in clinical practice. Trial registration PROSPERO CRD42020176682; https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=176682.

2017 ◽  
Vol 22 (9) ◽  
pp. 1049-1055 ◽  
Author(s):  
Karen‐Lise G. Spindler ◽  
Anders K. Boysen ◽  
Niels Pallisgård ◽  
Julia S. Johansen ◽  
Josep Tabernero ◽  
...  

Oncotarget ◽  
2018 ◽  
Vol 9 (36) ◽  
pp. 24514-24524 ◽  
Author(s):  
Xin Wang ◽  
Xia-Qing Shi ◽  
Peng-Wei Zeng ◽  
Fong-Ming Mo ◽  
Zi-Hua Chen

Gene ◽  
2018 ◽  
Vol 679 ◽  
pp. 328-334 ◽  
Author(s):  
Linyan Chen ◽  
Yi Zhang ◽  
Yuan Cheng ◽  
Dan Zhang ◽  
Sha Zhu ◽  
...  

2016 ◽  
Vol 7 (9) ◽  
pp. 1105-1113 ◽  
Author(s):  
Shiva Basnet ◽  
Zhen-yu Zhang ◽  
Wen-qiang Liao ◽  
Shu-heng Li ◽  
Ping-shu Li ◽  
...  

2014 ◽  
Vol 17 (2) ◽  
pp. 67-71 ◽  
Author(s):  
D. T. Korkmaz ◽  
P. G. Atak ◽  
Ç. Çelik

Abstract Familial Mediterranean fever (FMF) is an autosomal recessive disorder characterized by fever and serosal inflammation. The reasons for the disorder are mutations in the Mediterranean fever (MEFV) gene; the most common of which are M694V, M680I, M694I and V726A. In this study, we aimed to screen these common mutations of the MEFV gene and then determine the prevalence of FMF according to these mutations in Adıyaman, Southeast Anatolia, Turkey. Seven hundred and sixty-seven healthy individuals from the region of Adıyaman participated in the study. Polymerase chain reaction-amplification refractory mutation system (PCR-ARMS) methods were used to determine the common mutations of the MEFV gene. Twenty-six (3.9%) individuals had only one mutation in the MEFV gene, 25 individuals were heterozygous and one person was homozygous for the V726A mutation (0.15%). In the present study, the V726A mutation (50.0%) was the most frequent, followed by M694V (38.5%), M680I (7.7%) and M694I (3.8%). It was seen that the carrier rate was very low and the prevalence of FMF was 0.15%, according to the common mutations of the MEFV gene in Adıyaman, Southeast Anatolia, Turkey.


Sign in / Sign up

Export Citation Format

Share Document