Published online Jul 7, 2024. doi: 10.3748/wjg.v30.i25.3140
Revised: May 11, 2024
Accepted: June 7, 2024
Published online: July 7, 2024
Processing time: 109 Days and 19.3 Hours
This editorial comments on the article entitled “Stage at diagnosis of colorectal cancer through diagnostic route: Who should be screened?” by Agatsuma et al, who conducted a retrospective study aiming at clarifying the stage at colorectal cancer (CRC) diagnosis based on different diagnostic routes. We share our opinion about CRC screening programs. The current situation suggests the need for a more specific and targeted population for CRC screening.
Core Tip: We comment on a retrospective study by Agatsuma et al on the early-stage detection of colorectal cancer (CRC) in three groups based on different diagnostic routes. We share our opinion about this study and further discuss the current status of CRC screening in different countries and regions. We believe that a more specific and targeted population is necessary for the better implementation of CRC screening.
- Citation: Zhou NY, Lin YX, Chen LX, Ye LS, Hu B. Refining the targeted population and achieving better for colorectal cancer screening. World J Gastroenterol 2024; 30(25): 3140-3142
- URL: https://www.wjgnet.com/1007-9327/full/v30/i25/3140.htm
- DOI: https://dx.doi.org/10.3748/wjg.v30.i25.3140
Colorectal cancer (CRC) is a common malignant tumor worldwide and its screening facilitates early diagnosis and may ultimately improve patient prognosis[1]. Screening should begin at age 50 years in those without a high-risk family history and at age 40 years or age 45 years in those with a family history of CRC[2,3]. Current screening options include guaiac fecal occult blood testing, the fecal immunochemical test (FIT), stool DNA-FIT (sDNA-FIT), colonoscopy, flexible sigmoidoscopy and computed tomography, among which colonoscopy and FIT are the primary screening modalities for CRC screening[3].
We read with great interest an article entitled “Stage at diagnosis of colorectal cancer through diagnostic route: Who should be screened?” by Agatsuma et al[4]. They conducted a retrospective study on the early detection of CRC in three groups based on different diagnostic routes. In this study, a total of 2083 patients diagnosed with CRC between January 2016 and December 2019 were evaluated. The patients were divided into three groups: cancer screening group, follow-up group and symptomatic group. Results showed that the early-stage CRC detection rate of follow-up group was higher than that of symptomatic group (57.3% vs 23.9%, P < 0.001) and was comparable to that of cancer screening group (57.3% vs 59.5%, P = 0.493). Agatsuma et al[4] concluded that CRC screening should be recommended, especially for patients without periodical hospital visits for comorbidities.
Early detection of CRC is absolutely essential for a better prognosis of the patients[5]. Despite the effectiveness of CRC screening, its implementation is barely satisfactory possibly due to factors such as inadequate publicity and limited human and financial resources, although guidelines vary from country to country due to different conditions[6,7]. Current situation suggests a need for a more specific, and targeted population for CRC screening.
Various technologies, such as FITs, colonoscopy, sigmoidoscopy, and computed tomography, can aid in CRC detection[8]. Some of those techniques are applied to follow-up examination for patients with other comorbidities, during which CRCs may be accidentally found. Those follow-up examinations for patients with comorbidities plays a role in cancer screening, suggesting that the need for CRC screening may be more urgent for people without regular follow-up examinations. This might relate to the easy access for publics to advanced medical technologies in some countries and regions. For instance, in China, people have easy access to a wide range of advanced medical technologies. Computed tomography, colonoscopy, and other examinations are often carried out in hospitals at all levels.
Despite the encouraging results shown in this study, we highly agree with Agatsuma et al[4] that further investigations are warranted. In our opinion, the type of comorbidities, specific examination during follow-up and frequency of follow-up examinations necessitate further analysis. In-depth studies may help refine the targeted population for cancer screening programs without excluding eligible individuals.
The work by Agatsuma et al[4] provides us with an enlightening way to identify the population for whom CRC screening should be particularly recommended, positively impacting the implementation of CRC screening programs.
1. | Friedrich K, Grüter L, Gotthardt D, Eisenbach C, Stremmel W, Scholl SG, Rex DK, Sieg A. Survival in patients with colorectal cancer diagnosed by screening colonoscopy. Gastrointest Endosc. 2015;82:133-137. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 1.7] [Reference Citation Analysis (0)] |
2. | Gupta N, Kupfer SS, Davis AM. Colorectal Cancer Screening. JAMA. 2019;321:2022-2023. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 29] [Cited by in F6Publishing: 39] [Article Influence: 7.8] [Reference Citation Analysis (0)] |
3. | Shaukat A, Kahi CJ, Burke CA, Rabeneck L, Sauer BG, Rex DK. ACG Clinical Guidelines: Colorectal Cancer Screening 2021. Am J Gastroenterol. 2021;116:458-479. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 160] [Cited by in F6Publishing: 358] [Article Influence: 119.3] [Reference Citation Analysis (0)] |
4. | Agatsuma N, Utsumi T, Nishikawa Y, Horimatsu T, Seta T, Yamashita Y, Tanaka Y, Inoue T, Nakanishi Y, Shimizu T, Ohno M, Fukushima A, Nakayama T, Seno H. Stage at diagnosis of colorectal cancer through diagnostic route: Who should be screened? World J Gastroenterol. 2024;30:1368-1376. [PubMed] [DOI] [Cited in This Article: ] [Reference Citation Analysis (6)] |
5. | Frazier AL, Colditz GA, Fuchs CS, Kuntz KM. Cost-effectiveness of screening for colorectal cancer in the general population. JAMA. 2000;284:1954-1961. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 428] [Cited by in F6Publishing: 417] [Article Influence: 17.4] [Reference Citation Analysis (0)] |
6. | Li N, Lu B, Luo C, Cai J, Lu M, Zhang Y, Chen H, Dai M. Incidence, mortality, survival, risk factor and screening of colorectal cancer: A comparison among China, Europe, and northern America. Cancer Lett. 2021;522:255-268. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 13] [Cited by in F6Publishing: 170] [Article Influence: 56.7] [Reference Citation Analysis (0)] |
7. | Chen H, Li N, Ren J, Feng X, Lyu Z, Wei L, Li X, Guo L, Zheng Z, Zou S, Zhang Y, Li J, Zhang K, Chen W, Dai M, He J; group of Cancer Screening Program in Urban China (CanSPUC). Participation and yield of a population-based colorectal cancer screening programme in China. Gut. 2019;68:1450-1457. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 106] [Cited by in F6Publishing: 195] [Article Influence: 39.0] [Reference Citation Analysis (0)] |
8. | Burnett-Hartman AN, Lee JK, Demb J, Gupta S. An Update on the Epidemiology, Molecular Characterization, Diagnosis, and Screening Strategies for Early-Onset Colorectal Cancer. Gastroenterology. 2021;160:1041-1049. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 119] [Cited by in F6Publishing: 140] [Article Influence: 46.7] [Reference Citation Analysis (0)] |