The diagnostic accuracy of circulating free DNA for the detection of KRAS mutation status in colorectal cancer: A meta-analysis

被引:11
作者
Xie, Wenli [1 ]
Xie, Li [2 ]
Song, Xianrang [1 ,2 ]
机构
[1] Shandong Univ, Shandong Canc Hosp, Jinan, Shandong, Peoples R China
[2] Shandong Univ, Shandong Acad Med Sci, Shandong Canc Hosp, Jinan, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
cfDNA; colorectal cancer; diagnostic; KRAS mutation; meta-analysis; CELL-FREE DNA; K-RAS MUTATIONS; PRIMARY TUMORS; SYSTEMATIC REVIEWS; PROGNOSTIC VALUE; BRAF MUTATIONS; DIGITAL-PCR; MUTANT-DNA; PLASMA DNA; TISSUE;
D O I
10.1002/cam4.1989
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
KRAS mutations have been reported as a reliable biomarker for epidermal growth factor receptor (EGFR) targeted therapy and are also associated with poor prognosis in colorectal cancer (CRC) patients. However, limitations of detecting KRAS mutations in tissues are obvious. KRAS mutations in the peripheral blood can be detected as an alternative to tissue analysis. The objective of this meta-analysis was to evaluate the diagnostic value of cfDNA (circulating free DNA) compared with tissues and to investigate the prognostic potential of cfDNA KRAS mutations in CRC patients. Searches were performed in PubMed, Embase, and Cochrane Library for published studies. We extracted true-positive (TP), false-positive (FP), false-negative (FN), true-negative (TN) values, survival rate of CRC patients with mutant and wild-type KRAS and calculated pooled sensitivity and specificity, positive/negative likelihood ratios [PLRs/NLRs], diagnostic odds ratios [DORs], and corresponding 95% confidence intervals [95% CIs]. We also generated a summary receiver operating characteristic (SROC) curve to evaluate the overall diagnostic potential. Totally, 31 relevant studies were recruited and used for the meta-analysis on the efficacy of cfDNA testing in detecting KRAS mutations. The pooled sensitivity, specificity, PLR, NLR, and DOR were 0.637 (95% CI: 0.607-0.666), 0.943 (95% CI: 0.930-0.954), 10.024 (95% CI: 6.912-14.535), 0.347 (95% CI: 0.269-0.447), and 37.882 (95% CI: 22.473-63.857), respectively. The area under the SROC curve was 0.9392. Together, the results suggest that detecting KRAS mutations in cfDNA has adequate diagnostic efficacy in terms of specificity. There is a promising role for cfDNA in the detection of KRAS mutations in CRC patients. However, prospective studies with larger patient cohorts are still required before definitive conclusions of the prognostic potential of cfDNA KRAS mutations in CRC patients were drawn.
引用
收藏
页码:1218 / 1231
页数:14
相关论文
共 64 条
[1]   Extended RAS Gene Mutation Testing in Metastatic Colorectal Carcinoma to Predict Response to Anti-Epidermal Growth Factor Receptor Monoclonal Antibody Therapy: American Society of Clinical Oncology Provisional Clinical Opinion Update 2015 [J].
Allegra, Carmen J. ;
Rumble, R. Bryan ;
Hamilton, Stanley R. ;
Mangu, Pamela B. ;
Roach, Nancy ;
Hantel, Alexander ;
Schilsky, Richard L. .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (02) :179-+
[2]   Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer [J].
Amado, Rafael G. ;
Wolf, Michael ;
Peeters, Marc ;
Van Cutsem, Eric ;
Siena, Salvatore ;
Freeman, Daniel J. ;
Juan, Todd ;
Sikorski, Robert ;
Suggs, Sid ;
Radinsky, Robert ;
Patterson, Scott D. ;
Chang, David D. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (10) :1626-1634
[3]  
[Anonymous], REV CURRENT STATUS K
[4]  
[Anonymous], MIDAS COMP GRAPH ROU
[5]  
Beranek Martin, 2016, Acta Medica (Hradec Kralove), V59, P54, DOI 10.14712/18059694.2016.54
[6]   Treatment monitoring in metastatic colorectal cancer patients by quantification and KRAS genotyping of circulating cell-free DNA [J].
Berger, Andreas W. ;
Schwerdel, Daniel ;
Welz, Hanna ;
Marienfeld, Ralf ;
Schmidt, Stefan A. ;
Kleger, Alexander ;
Ettrich, Thomas J. ;
Seufferlein, Thomas .
PLOS ONE, 2017, 12 (03)
[7]   Detection of Circulating Tumor DNA in Early- and Late-Stage Human Malignancies [J].
Bettegowda, Chetan ;
Sausen, Mark ;
Leary, Rebecca J. ;
Kinde, Isaac ;
Wang, Yuxuan ;
Agrawal, Nishant ;
Bartlett, Bjarne R. ;
Wang, Hao ;
Luber, Brandon ;
Alani, Rhoda M. ;
Antonarakis, Emmanuel S. ;
Azad, Nilofer S. ;
Bardelli, Alberto ;
Brem, Henry ;
Cameron, John L. ;
Lee, Clarence C. ;
Fecher, Leslie A. ;
Gallia, Gary L. ;
Gibbs, Peter ;
Le, Dung ;
Giuntoli, Robert L. ;
Goggins, Michael ;
Hogarty, Michael D. ;
Holdhoff, Matthias ;
Hong, Seung-Mo ;
Jiao, Yuchen ;
Juhl, Hartmut H. ;
Kim, Jenny J. ;
Siravegna, Giulia ;
Laheru, Daniel A. ;
Lauricella, Calogero ;
Lim, Michael ;
Lipson, Evan J. ;
Marie, Suely Kazue Nagahashi ;
Netto, George J. ;
Oliner, Kelly S. ;
Olivi, Alessandro ;
Olsson, Louise ;
Riggins, Gregory J. ;
Sartore-Bianchi, Andrea ;
Schmidt, Kerstin ;
Shih, Ie-Ming ;
Oba-Shinjo, Sueli Mieko ;
Siena, Salvatore ;
Theodorescu, Dan ;
Tie, Jeanne ;
Harkins, Timothy T. ;
Veronese, Silvio ;
Wang, Tian-Li ;
Weingart, Jon D. .
SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (224)
[8]   Detection of PIK3CA mutations in circulating free DNA in patients with breast cancer [J].
Board, Ruth E. ;
Wardley, Andrew M. ;
Dixon, J. Michael ;
Armstrong, Anne C. ;
Howell, Sacha ;
Renshaw, Lorna ;
Donald, Emma ;
Greystoke, Alastair ;
Ranson, Malcolm ;
Hughes, Andrew ;
Dive, Caroline .
BREAST CANCER RESEARCH AND TREATMENT, 2010, 120 (02) :461-467
[9]   KRAS genotyping in rectal adenocarcinoma specimens with low tumor cellularity after neoadjuvant treatment [J].
Boissiere-Michot, Florence ;
Lopez-Crapez, Evelyne ;
Frugier, Helene ;
Berthe, Marie-Laurence ;
Ho-Pun-Cheung, Alexandre ;
Assenat, Eric ;
Maudelonde, Thierry ;
Lamy, Pierre-Jean ;
Bibeau, Frederic .
MODERN PATHOLOGY, 2012, 25 (05) :731-739
[10]   Liquid biopsy: monitoring cancer-genetics in the blood [J].
Crowley, Emily ;
Di Nicolantonio, Federica ;
Loupakis, Fotios ;
Bardelli, Alberto .
NATURE REVIEWS CLINICAL ONCOLOGY, 2013, 10 (08) :472-484