Value of combined serum CEA, CA72-4, and CA19-9 marker detection in diagnosis of colorectal cancer.
Carbohydrate antigen 19–9
Carbohydrate antigen 72–4
Carcinoembryonic antigen
Colorectal cancer
Tumor markers
Journal
Techniques in coloproctology
ISSN: 1128-045X
Titre abrégé: Tech Coloproctol
Pays: Italy
ID NLM: 9613614
Informations de publication
Date de publication:
15 Feb 2024
15 Feb 2024
Historique:
received:
10
05
2023
accepted:
18
10
2023
medline:
15
2
2024
pubmed:
15
2
2024
entrez:
15
2
2024
Statut:
epublish
Résumé
The aim of this study was to examine whether the combination of serum tumor markers (carcinoembryonic antigen [CEA], carbohydrate antigen [CA]72-4, CA19-9) improves sensitivity and accuracy in the diagnosis of colorectal cancer and precancerous lesion tubular adenoma. An automatic electrochemiluminescence immunoassay with matched kits (ECLIA) was performed on a Roche Cobas e411 analyzer to determine the levels of serum CEA, CA72-4, and CA19-9 in 35 patients with early colorectal cancer, 87 patients with tubular adenoma, and 58 healthy people undergoing colonoscopy after positive fecal immunochemical test (FIT) in a colorectal cancer screening program 2021 January to April. The values of these three tumor markers in the diagnosis of colorectal cancer and tubular adenoma were analyzed. 180 patients (92 female and 88 male) were included into the study. We compared serum CEA, CA72-4 and CA19-9 markers among 3 groups: healthy people (mean age 64,0 ±8,6), patients with tubular adenoma (mean age 62,7 ± 6,4) and colorectal cancer (mean age 59,2 ±6,2). The levels of serum CEA, CA72-4, and CA19-9 were higher in the colorectal cancer group than in the tubular adenoma group and healthy subjects, and these differences were significant (p < 0.05). The combination of CEA, CA72-4, and CA19-9 had a higher diagnostic value for colorectal cancer compared to single markers, and the positive detection rate was 54.3%. The diagnostic power when using all three markers was the best, and applied for colorectal cancer and tubular adenoma. The combination of CA72-4, CEA, and CA19-9 markers increases the sensitivity and accuracy in the diagnosis of colorectal cancer and can thus be considered an important tool for early colorectal diagnosis.
Sections du résumé
BACKGROUND
BACKGROUND
The aim of this study was to examine whether the combination of serum tumor markers (carcinoembryonic antigen [CEA], carbohydrate antigen [CA]72-4, CA19-9) improves sensitivity and accuracy in the diagnosis of colorectal cancer and precancerous lesion tubular adenoma.
METHODS
METHODS
An automatic electrochemiluminescence immunoassay with matched kits (ECLIA) was performed on a Roche Cobas e411 analyzer to determine the levels of serum CEA, CA72-4, and CA19-9 in 35 patients with early colorectal cancer, 87 patients with tubular adenoma, and 58 healthy people undergoing colonoscopy after positive fecal immunochemical test (FIT) in a colorectal cancer screening program 2021 January to April. The values of these three tumor markers in the diagnosis of colorectal cancer and tubular adenoma were analyzed.
RESULTS
RESULTS
180 patients (92 female and 88 male) were included into the study. We compared serum CEA, CA72-4 and CA19-9 markers among 3 groups: healthy people (mean age 64,0 ±8,6), patients with tubular adenoma (mean age 62,7 ± 6,4) and colorectal cancer (mean age 59,2 ±6,2). The levels of serum CEA, CA72-4, and CA19-9 were higher in the colorectal cancer group than in the tubular adenoma group and healthy subjects, and these differences were significant (p < 0.05). The combination of CEA, CA72-4, and CA19-9 had a higher diagnostic value for colorectal cancer compared to single markers, and the positive detection rate was 54.3%. The diagnostic power when using all three markers was the best, and applied for colorectal cancer and tubular adenoma.
CONCLUSIONS
CONCLUSIONS
The combination of CA72-4, CEA, and CA19-9 markers increases the sensitivity and accuracy in the diagnosis of colorectal cancer and can thus be considered an important tool for early colorectal diagnosis.
Identifiants
pubmed: 38358422
doi: 10.1007/s10151-023-02873-4
pii: 10.1007/s10151-023-02873-4
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
33Informations de copyright
© 2024. Springer Nature Switzerland AG.
Références
Sung H, Ferlay J, Siegel RL et al (2021) Global Cancer Statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 71(3):209–249. https://doi.org/10.3322/caac.21660 .
doi: 10.3322/caac.21660
pubmed: 33538338
Calon A, Lonardo E, Berenguer-Llergo A et al (2015) Stromal gene expression defines poor-prognosis subtypes in colorectal cancer. Nat Genet 47(4):320–329. https://doi.org/10.1038/ng.3225
doi: 10.1038/ng.3225
pubmed: 25706628
Dulskas A, Gaizauskas V, Kildusiene I, Samalavicius NE, Smailyte G (2020) Improvement of survival over time for colorectal cancer patients: a population-based study. J Clin Med 9(12):4038. https://doi.org/10.3390/jcm9124038
doi: 10.3390/jcm9124038
pubmed: 33327538
pmcid: 7765021
ASGE Standards of Practice Committee, Fisher DA, Shergill AK et al (2013) Role of endoscopy in the staging and management of colorectal cancer. Gastrointest Endosc 78:8–12. https://doi.org/10.1016/j.gie.2013.04.163
doi: 10.1016/j.gie.2013.04.163
Kahi CJ, Boland CR, Dominitz JA et al (2016) Colonoscopy surveillance after colorectal cancer resection: recommendations of the US multi-society task force on colorectal cancer. Gastroenterology 150:758–768.e711. https://doi.org/10.1053/j.gastro.2016.01.001 .
Loeve F, Brown ML, Boer R, van Ballegooijen M, van Oortmarssen GJ, Habbema JD (2000) Endoscopic colorectal cancer screening: a cost-saving analysis. J Natl Cancer Inst 92:557–563
doi: 10.1093/jnci/92.7.557
pubmed: 10749911
Garborg K, Holme Ø, Løberg M, Kalager M, Adami HO, Bretthauer M (2013) Current status of screening for colorectal cancer. Ann Oncol 24:1963–1972. https://doi.org/10.1093/annonc/mdt157
doi: 10.1093/annonc/mdt157
pubmed: 23619033
Anderson JC, Fortinsky RH, Kleppinger A, Merz-Beyus AB, Huntington CG 3rd, Lagarde S (2011) Predictors of compliance with free endoscopic colorectal cancer screening in uninsured adults. J Gen Intern Med 26:875–880. https://doi.org/10.1007/s11606-011-1716-7
doi: 10.1007/s11606-011-1716-7
pubmed: 21499823
pmcid: 3138985
Niv Y, Sperber AD (1995) Sensitivity, specificity, and predictive value of fecal occult blood testing (Hemoccult II) for colorectal neoplasia in symptomatic patients: a prospective study with total colonoscopy. Am J Gastroenterol 90:1974–1977
pubmed: 7485003
Allison JE, Tekawa IS, Ransom LJ, Adrain AL (1996) Improving the fecal occult-blood test. N Engl J Med 334:1607–1608. https://doi.org/10.1056/NEJM199606133342414
doi: 10.1056/NEJM199606133342414
pubmed: 8628349
Allison JE, Tekawa IS, Ransom LJ, Adrain AL (1996) A comparison of fecal occult-blood tests for colorectal-cancer screening. N Engl J Med 334:155–159. https://doi.org/10.1056/NEJM199601183340304
doi: 10.1056/NEJM199601183340304
pubmed: 8531970
Lieberman DA, Weiss DG, Bond JH et al (2000) Use of colonoscopy to screen asymptomatic adults for colorectal cancer. N Engl J Med 343(3):162–168. https://doi.org/10.1056/NEJM2000072034303018
doi: 10.1056/NEJM2000072034303018
pubmed: 10900274
Calderwood AH, Lasser KE, Roy HK (2016) Colon adenoma features and their impact on risk of future advanced adenomas and colorectal cancer. World J Gastrointest Oncol 8(12):826–834. https://doi.org/10.4251/wjgo.v8.i12.826
doi: 10.4251/wjgo.v8.i12.826
pubmed: 28035253
pmcid: 5156849
Hisabe T, Hirai F, Matsui T (2014) Development and progression of colorectal cancer based on follow-up analysis. Dig Endosc 26:73–77. https://doi.org/10.1111/den.1227610
doi: 10.1111/den.1227610
pubmed: 24750153
Edwards BK, Ward E, Kohler BA et al (2010) Annual report to the nation on the status of cancer, 1975–2006, featuring colorectal cancer trends and impact of interventions (risk factors, screening, and treatment) to reduce future rates. Cancer 116(3):544–573. https://doi.org/10.1002/cncr.2476011
doi: 10.1002/cncr.2476011
pubmed: 19998273
Dulskas A, Poskus T, Kildusiene I et al (2021) National colorectal cancer screening program in Lithuania: description of the 5-year performance on population level. Cancers (Basel) 13(5):1129. https://doi.org/10.3390/cancers13051129.PMID:33800772;PMCID:PMC7961359
doi: 10.3390/cancers13051129.PMID:33800772;PMCID:PMC7961359
pubmed: 33800772
Meklin J, SyrjÄnen K, Eskelinen M (2020) Fecal occult blood tests in colorectal cancer screening: systematic review and meta-analysis of traditional and new-generation fecal immunochemical tests. Anticancer Res 40(7):3591–3604. https://doi.org/10.21873/anticanres.14349
doi: 10.21873/anticanres.14349
pubmed: 32620599
Park HJ, Ahn JY, Jung HY et al (2014) Clinical characteristics and outcomes for gastric cancer patients aged 18–30 years. Gastric Cancer 17:649–660
Nam DH, Lee YK, Park JC et al (2013) Prognostic value of early postoperative tumor marker response in gastric cancer. Ann Surg Oncol 20:3905–3911
Parchur AK, Sharma G, Jagtap JM et al (2018) Vascular in⁃terventional radiology⁃guided photothermal therapy of colorectal cancer liver metastasis with theranostic gold nanorods. ACS Nano 12(7):6597–6611
Türk G, Eldem G, Kılıçkap S et al (2019) Outcomes of radioembolization in patients with chemorefractory colorectal cancer liver metastasis: a single-center experience. J Gastrointest Cancer 50(2):236–243. https://doi.org/10.1007/s12029-018-0053-z
doi: 10.1007/s12029-018-0053-z
pubmed: 29354877
Baidoun F, Elshiwy K, Elkeraie Y et al (2021) Colorectal cancer epidemiology: recent trends and impact on outcomes. Curr Drug Targets 22:998–1009
Adam R, de Gramont A, Figueras J et al (2015) Managing synchronous liver metastases from colorectal cancer: a multidisciplinary international consensus. Cancer Treat Rev 41(9):729–41. https://doi.org/10.1016/j.ctrv.2015.06.006
Zhang S-Y, Lin M, Zhang H-B (2015) Diagnostic value of carcinoembryonic antigen and carcinoma antigen 19–9 for colorectal carcinoma. Int J Clin Exp Pathol 8:9404–9409
pubmed: 26464695
pmcid: 4583927
Filella X, Molina R, Grau JJ et al (1992) Prognostic value of CA 19.9 levels in colorectal cancer. Ann Surg 216:55–59
Zhang L-N, OuYang P-Y, Xiao W-W et al (2015) Elevated CA19-9 as the most significant prognostic factor in locally advanced rectal cancer following neoadjuvant chemoradiotherapy. Medicine 94:e1793
doi: 10.1097/MD.0000000000001793
pubmed: 26559251
pmcid: 4912245
Keller G, Vogelsang H, Becker I et al (2004) Germline mutations of the E-cadherin(CDH1) and TP53 genes, rather than of RUNX3 and HPP1, contribute to genetic predisposition in German gastric cancer patients. J Med Genet 41(6):e89. https://doi.org/10.1136/jmg.2003.015594
doi: 10.1136/jmg.2003.015594
pubmed: 15173255
pmcid: 1735803
Sun Z, Zhang N (2014) Clinical evaluation of CEA, CA19-9, CA72-4 and CA125 in gastric cancer patients with neoadjuvant chemotherapy. World J Surg Onc 12:397. https://doi.org/10.1186/1477-7819-12-397
doi: 10.1186/1477-7819-12-397