Abstract

Introductionthe most reliable screening tool for colorectal cancer, colonoscopy, is not readily accessible in resource-deprived settings of KwaZulu-Natal. The aim of this study was to determine whether serum carcinoembryonic antigen (CEA) levels in patients symptomatic for lower gastrointestinal (GI) pathology correlates with the histological presence and severity of primary colorectal cancer in a large referral centre. Perhaps CEA may have a larger role as a marker for colorectal cancer (CRC) development in these resource deprived communities.Methodsthis study was a retrospective analysis of prospectively collected clinical data of 380 pretreatment patients with colorectal cancer attending a tertiary referral centre in KwaZulu-Natal. Data were analyzed using descriptive statistics and findings were compared with those from the existing literature.Resultsthe mean CEA level of the study population was 170.0 ± 623.3 μg/l. The number of participants with a CEA level <5 μg/l was 151 (39.74%) whilst the majority 229 (60.26%) had a CEA level ≥ 5 μg/l. There was no significant correlation between CEA levels and gender (p=0.8) or age (p=0.6). CEA levels were highest in the black African race group. Pairwise comparison demonstrated a statistically significant difference between the black and Indian population groups (p=0.02). The current study demonstrates an upregulation of CEA as the stage of CRC progresses (p<0.0001).Conclusionthere was no significant difference in CEA levels across age and gender. A positive correlation was noted between CEA level and stage of CRC. Carcinoembryonic antigen levels were highest in the black race group. Low sensitivity of CEA as a screening test for CRC was confirmed.

Highlights

  • Colorectal cancer (CRC) is the third most common malignancy in the world [1]

  • This study reports no significant difference in carcinoembryonic antigen (CEA) levels across age or gender

  • The CEA levels were found to be highest in the black African race group and the present series confirms a low sensitivity of CEA as a diagnostic test for CRC

Read more

Summary

Introduction

Colorectal cancer (CRC) is the third most common malignancy in the world [1]. The global incidence of CRC is projected to rise up to 60% by 2030 [2,3]. More than one million new cases are diagnosed per annum and 530,000 deaths are reported per year. Colorectal cancer evolves across four distinct carcinogenic conduits: the chromosomal instability pathway [4], the microsatellite instability pathway [4], the cytosine-phosphate-guanine (CpG) methylator pathway-1 [5] and pathway-2 [6]. The slow growth of CRC warrants early screening to reduce both the incidence of and mortality from the disease. The aim of screening should be to detect CRC at a relatively early stage (stage 1 and 2). Currently the most reliable diagnostic tool, namely colonoscopy is not accessible in resource-deprived settings

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call