Epidemiological insights into colorectal cancer in northwestern Algeria
Salah Eddine El Herrag1,2,a, Soraya Moulessehoul2, Douniazad El Mehadji2,b, Djamila Yekrou3 and Méghit Boumediène Khaled1,2,c
1Laboratoire de Nutrition, Pathologie, Agro-Biotechnologie et Santé (Lab-NuPABS), Faculty of Natural and Life Sciences, Djillali Liabes University, Sidi Bel Abbes 22000, Algeria
2Department of Biology Rectorat Ex ITMA, Faculty of Natural and Life Sciences, Djillali Liabes University, BP 89, Sidi Bel Abbes 22000, Algeria
3Department of Medical Oncology, Anti-Cancer Centre of Sidi Bel Abbes, Sidi Bel Abbes 22000, Algeria
ahttps://orcid.org/0000-0002-6483-4771
bhttps://orcid.org/0000-0002-0214-6383
chttps://orcid.org/0000-0001-5281-2498
Abstract
Objectives: The incidence of colorectal cancer (CRC) has exhibited regional variability in North Africa and the Middle East, with a steady increase in Algeria. Despite this trend, limited data exist on the epidemiology of CRC in northwestern Algeria. Our study aimed to investigate the epidemiological characteristics of CRC in this region.
Methods: We conducted a retrospective study examining 255 confirmed CRC cases through medical records from patients at the Sidi Bel Abbes anti-cancer centre.
Results: The mean age of the study participants was 59 ± 13 years. The results showed a higher incidence in males (57%) than in females, and colon (62%) than rectal cancer. Within this cohort, 47% had a pre-existing medical condition, while 39% had a family history of cancer. Adenocarcinomas were the prevailing histological subtype in 94% of CRC cases. Compared with colon cancer, rectal cancer was less often diagnosed at stage IV of the disease (OR = 0.75; 95% CI = 0.09, 4.86; p = 0.8) and more likely in early-onset patients (OR = 2.27; 95% CI = 1.25, 4.17; p = 0.007). Men were at a higher risk of being diagnosed with metastatic CRC primarily hepatic metastases (OR = 2.03; 95% CI = 1.07, 3.99; p = 0.033) and pulmonary metastases (OR = 2.50; 95% CI = 1.07, 6.59; p = 0.045).
Conclusion: This study may provide a comprehensive glimpse into CRC epidemiology in northwest Algeria. Understanding regional differences is the key to implementing specific preventive and interventional strategies.
Keywords: colorectal neoplasms, epidemiology, incidence, Algeria
Correspondence to: Salah Eddine El Herrag
Email: salaheddine.elherrag@univ-sba.dz
Published: 21/03/2024
Received: 22/12/2023
Publication costs for this article were supported by ecancer (UK Charity number 1176307).
Copyright: © the authors; licensee ecancermedicalscience. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Introduction
Colorectal cancer (CRC) is a major global health concern with varying incidence rates among populations worldwide. In Africa, the age-standardised rate per 100,000, was 8.4 [1], which is generally lower than that in other parts of the world, with notable heterogeneity from regional and country-level perspectives [2]. Data from the Middle East and North Africa show a comparatively rising trend [3]. CRC has emerged as a growing health concern in Algeria owing to the severity of the disease, as its incidence rate continues to rise. The number of new CRC cases has significantly increased in recent years. In 2020, GLOBOCAN reported that the number of new CRC cases identified in Algeria nearly doubled from the previous year, marking a 94% increase in new cases. This alarming trend has allowed CRC to rank second in terms of cancer incidence in Algeria after breast cancer and to have the third highest mortality rate after lung and breast cancer in both sexes and all age categories [1, 4].
CRC is a complex and multifactorial neoplasm that is influenced by a variety of factors, including genetics, environment and lifestyle [5–8]. Previous studies have shown that the incidence, prevalence and clinical characteristics of CRC vary depending on geographic and demographic factors [3, 9–11].
Data on CRC burden in the northwestern region of Algeria remain scarce. On this basis, we have attempted through the present investigation to shed light on some of the demographic, epidemiological, clinical, histological and therapeutic aspects of CRC patients in the region. This study will contribute to expanding knowledge on the epidemiology of CRC globally with data from the Algerian population and, specifically, the province of Sidi Bel Abbes, located in the northwest of the country.
This study aimed to assess CRC’s epidemiological profile in Algeria’s western region, which can provide new insights into the incidence and risk factors for CRC in this population.
Methods
Study design and setting
We performed a retrospective cohort investigation involving patients with histologically confirmed CRC identified from patient records admitted to the anti-cancer centre of the University Hospital of Sidi Bel Abbes, Algeria. The reporting of the study adhered to the guidelines outlined in the strengthening the reporting of observational studies in epidemiology checklist.
The anti-cancer centre is a regional health facility designed for the care of patients with cancer in the western and southwestern regions of the country. The study spans 4 years (January 2018 to December 2021).
The study was approved by the Biology Department Committee of the Natural and Life Sciences Faculty of Djillali Liabes University and the Department of Medical Oncology of the Anti-cancer Centre of Sidi Bel Abbes. The ethics committee of University Hospital Centre Abdelkader Hassani of Sidi bel Abbes approved the study (Ref: Decision No 5).
Study participants
Subjects were identified through paper-based medical records of patients admitted to the centre with a confirmed diagnosis of a primary CRC tumour. All patients meeting the eligibility criteria i.e., presenting a histologically confirmed primary CRC, were included in the final analysis without applying any exclusion criteria.
Variables
Demographics
Data on age, sex, anatomic site, socioeconomic status, higher educational status, height and weight were collected directly from the patient’s medical records. Patients were categorised into two groups: those with early-onset CRC (diagnosed before the age of 50 years) and those with late-onset CRC (diagnosed at 50 years of age or older). Body mass index (BMI) was calculated by dividing the patient’s weight (in kg) by the square of their height (in m). Subjects were subsequently categorised based on their BMI into distinct groups: underweight (BMI ≤18.4 kg/m2), normal weight (BMI 18.5–24.9 kg/m2), overweight (BMI 25.0–39.9 kg/m2), and obese (BMI ≥ 40.0 kg/m2), in accordance with the criteria established by the centres for disease control and prevention [12]. Patients were stratified according to anatomical site (colon or rectum C18-C20) [13].
Personal medical, surgical and family history of cancer
We extracted information related to the personal medical, surgical, and cancer family history of all patients included in the study. First-degree relatives included mothers, fathers, daughters, sons, sisters and brothers. On the other hand, individuals categorised as second-degree relatives encompass progenitors and descendants spanning multiple generations as well as collateral relatives such as paternal and maternal aunts, uncles, nieces, nephews, grandparents and grandchildren. Other personal medical history encompasses comorbidities beyond hypertension, diabetes and stroke, while other personal surgical history includes surgical interventions apart from appendicectomy or cholecystectomy.
Histological classification, staging and metastasis
We collected information on the tumour histological classification, staging, and metastasis status. The American Joint Committee on Cancer cancer staging system, specifically the tumour, node and metastasis scoring algorithm, is employed for CRC staging [14].
Treatment and symptoms
The centre provides treatment for CRC patients including chemotherapy, radiotherapy and targeted therapy. Symptoms at diagnosis were retrieved from the medical records.
Lifestyle factors and biomarkers
Data collected included information on biomarkers, including carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9, also denoted as cancer antigen 19-9 or sialyl Lewis A antigen (CA 19-9) levels, as well as the mutational status of Kirsten rat sarcoma virus (KRAS), Neuroblastoma RAS (NRAS) and B-Raf Proto-Oncogene, Serine/Threonine Kinase (BRAF). These biomarkers are acknowledged for their potential to aid in CRC diagnosis, prognosis and management [15, 16]. Additionally, patients’ records also contained data on smoking and alcohol consumption, providing valuable information for assessing potential risk factors and their influence on the disease.
Statistical methods
Numerical variables were summarised using means (measures of central tendency), standard deviations, and ranges (measures of dispersion). Categorical variables, on the other hand, were summarised using frequencies and percentages from the total number of observations, and missing data were not accounted for in percentage calculations. The Wilcoxon rank-sum test was employed to examine the differences between two groups of continuous distribution.
Pearson’s chi-squared test was applied to ascertain the significance of the association between categories. Alternatively, Fisher’s exact test was utilised to ascertain the significance of the association between two categories in the case of a small sample size. The logistic regression model using maximum likelihood estimation was used to predict the probability of a binary outcome and calculate the odds ratios (OR) and their 95% confidence intervals (CI) to assess potential correlations between age (early-onset versus late-onset), sex (male versus female), and anatomic site (colon versus rectum) and patients’ characteristics. The results of all statistical tests were deemed significant at a p-value of <0.05 threshold. All statistical analyses were performed using the R statistical program (version 4.3.1) [17, 18].
Results
Participants
Our study included 255 confirmed CRC patients diagnosed at the level of the anti-cancer centre of Sidi Bel Abbes, located in the northwestern region of Algeria.
Descriptive data
57% of patients were male (n = 145), and 43% were female (n = 110). Colon cancer was the most frequent anatomical site, accounting for 62% (n = 158) of all CRC cases. The mean age of the study population was 59 ± 13 years (range, 20–91 years); 93% were 40 years or older, and 78% were diagnosed at 50 years of age or more. Female patients were slightly younger than their male counterparts, with a mean age of 58 ± 13 years (range, 22–89 years) and 60 ± 13 years (range, 20–91 years) (p = 0.300) for males (Table 1). We noticed a significant difference in the mean age at diagnosis according to the CRC anatomical site (mean age = 61 ± 13 for colon cancer versus 57 ± 13 for rectum, p = 0.011). Patients aged 50 years or older demonstrated a higher likelihood of being diagnosed with colon cancer than rectal cancer (OR = 2.27; 95% CI = 1.25, 4.17; p = 0.007).
Table 1. Patients’ demographic characteristics stratified by sex, tumour anatomic site and age category.
Despite the limited available data, significant sex-based disparities were observed where female patients were more likely to have a low socioeconomic level (p = 0.031) and less likely to have a higher educational status (p = 0.014) compared to male patients.
The mean height of the overall population was 1.66 ± 0.10 m, and the average weight was 63 ± 13 kg. Male patients were taller (mean height = 1.71 ± 0.08 versus 1.58 ± 0.07 m; p < 0.001). In addition, men had higher weight compared to female patients (mean weight = 65 ± 13 versus 60 ± 14 kg; p = 0.009).
Personal medical, surgical and family history of cancer
All CRC patients’ personal medical, surgical and family histories were analysed. The results showed that 119 (47%) patients had a pre-existing medical condition in which hypertension was the most prevalent, manifesting in 49 (19%) of the patients, followed by diabetes, which was present in 36 (14%) of the studied population (Table 2 and Figure 1a). Patients with a positive personal medical history had a significantly higher mean age (64 ± 11 years) than those without (55 ± 13 years) (p < 0.001) and the risk increased by 7% for every additional year of age. (OR = 1.07; 95% CI = 1.05, 1.10; p < 0.001). In addition, they had a higher mean BMI (24.1 ± 4.8; p = 0.008), higher frequency of metastasis (39%; p = 0.045), and hepatic metastases (31%; p = 0.002). CRC patients with pre-existing onset of diabetes were older (65 ± 10; p < 0.001), had higher mean BMI (25.0 ± 5.1; p = 0.020), and had higher CA 19-9 levels (reference range ≥ 35 U/mL) compared to those without diabetes (50% versus 25%; p = 0.024). Moreover, CRC patients manifesting antecedent hypertension were older (68 ± 9 years; p < 0.001), experienced more incidents of stroke (6.1%; p = 0.024), had more cholecystectomies (14%; p = 0.001), and had higher CEA levels (≥ 5 ng/mL) (59%; p = 0.050).
Table 2. Age, sex, and anatomical-related differences of personal medical, surgical and family history of cancer.
Our study reported that 102 (40%) of CRC patients had undergone surgery. Of those who underwent surgery, 19 (19%) had an appendectomy and 11 (11%) underwent a cholecystectomy. Personal surgical history was more common in colon cancer patients 71 (45%) than in those with rectal cancer 31 (32%) (Figure 1b). This difference in surgical history between the two groups was statistically significant, with a value of p = 0.040. Patients with a personal surgical history were more likely to have colon than rectal cancer (OR = 1.74; 95% CI = 1.03, 2.97; p = 0.041) (Table 3 and Figure 1b). The same trend was noticed concerning appendectomy (p = 0.041), (OR = 3.47; 95% CI = 1.12, 15.2; p = 0.053). Patients with a positive surgical history had a significantly higher mean age (61 ± 13 years) compared to those without (58 ± 12 years) (p = 0.024), and the tumours were more localised in the colon (70%) than in the rectum (30%) (p = 0.040). The overweight and obesity categories showed a significant difference in CRC frequency based on surgical history (p = 0.023) and a significant difference in metastasis occurrence (40%; p = 0.036) and hepatic metastases (30%; p = 0.015). Patients who underwent appendectomy had more tumours localised in the colon than in the rectum (84% versus 16%; p = 0.041) and had lower CEA levels compared with those who did not undergo this type of surgery (10% versus 45%; p = 0.043).
A family history of cancer was present in 39% of CRC patients (Figure 1a). Of these patients, 24 (27%) reported a family history of CRC in one or more first-degree relatives, whereas 55 (61%) had one or multiple first-degree family members with other types of cancer. We noted a significantly higher prevalence of diabetes in CRC patients with a family history of cancer than in those with no such history (22%; p = 0.011).
Histological classification, staging and metastasis
Adenocarcinomas accounted for 94% of all CRC cases, of these, 54% were well differentiated. The proportion of stageable adenocarcinomas was 66%. Out of the cases that could be classified, 34% were stage III (Table 4). Patients with colon cancer had a higher probability of being diagnosed at stage IV than those with rectal cancer (75% versus 25%; p < 0.001). Stage IV CRC patients had higher CEA levels (≥ 5 ng/mL) (80%) compared with patients in other stages of the disease (p = 0.002).
Approximately one-third of the CRC patients in our study presented tumours with distant metastases. Hepatic and pulmonary metastases were the most frequent, accounting for 22% and 12% of all CRC cases in our study, respectively (Figure 2a). The difference between males and females regarding the presence of metastasis was significant (23% of females versus 39% of male patients; p = 0.010).
The occurrence of metastatic tumours was higher amongst male patients in comparison to females. The same trend was observed for liver and lung metastases (p = 0.031 and 0.040, respectively). Men developed hepatic and pulmonary metastases more often than women (OR = 2.03; 95% CI = 1.07, 3.99; p = 0.033) and (OR = 2.50; 95% CI = 1.07, 6.59; p = 0.045) respectively. CRC patients with metastasis presented higher CEA levels and lower CA 19-9 levels (74%; p < 0.001) and (46%; p < 0.001) respectively.
Figure 1. Personal medical, surgical and family history of cancer. (a): Proportions of CRC patients with pre-existing comorbidities, prior surgical history, and family history of cancer. (b): Proportions of CRC patients with personal, surgical, and family history of cancer stratified by CRC anatomic site, age group and sex.
Table 3. Association of clinical characteristics with the risk of CRC according to CRC anatomic site and sex.
Table 4. Histological classification, staging, and metastasis status according to sex, age and anatomic site.
Figure 2. Staging, metastasis and symptoms (a): Distribution of CRC patients according to tumour stage at diagnosis with a proportional breakdown of metastatic status. (b): Heatmap illustrating the distribution of symptoms in CRC patients according to sex, age group and tumour anatomic site. Each tile represents the percentage of patients with a specific symptom.
Symptoms and treatment
The symptoms leading to CRC diagnosis were nonspecific. The most frequently observed signs at the time of diagnosis were asthenia (50%), weight loss (42%), pain (42%), and colonic transit disorders including diarrhoea and constipation (40%). Late-onset CRC patients experienced weight loss more frequently (n = 83, 48%) than early-onset patients (n = 12, 24%) (p = 0.002), while diarrhoea was more frequent in rectal cancer patients (n = 23, 25 %) than in colon cancer patients (n = 14, 9.7%) (p = 0.001) (Figure 2b).
Over 70% of diagnosed CRC cases received at least one type of treatment or a combination at the facility level. Of these patients, 85% received chemotherapy, 34% were treated with targeted therapy, 20% with radiotherapy, and 18% with radiochemotherapy. No discernible statistically significant differences in treatment accessibility were noted between the males and females. 83% of CRC patients who received chemotherapy had late-onset disease, 35% received it in combination with targeted therapy, and 22% with radiotherapy.
Lifestyle behaviours and biomarkers
In the present study, information regarding KRAS mutation status was available for a cohort of 92 patients diagnosed with CRC (Table 5). Among these patients, 54 (59%) exhibited mutations in the KRAS gene, while the remaining 38 (41%) displayed a wild-type KRAS genotype. Similarly, data for 60 CRC patients regarding NRAS and BRAF mutation status were available showing that only 10% and 5% of these tumours presented mutations respectively.
Table 5. Biomarkers and lifestyle behaviours stratified by sex, tumour anatomic site, and age category.
Discussion
In summary, 255 CRC patients were included in our study. Of these patients, approximately 57% were males, indicating a slight male predominance in our sample. This finding is consistent with the global incidence data of CRC, which indicates that 55% of cases are male [1].
Moreover, the proportion of colon cancers among all CRC cases in our study generally agreed with those recorded worldwide. Nearly two-thirds (62%) of patients had tumours localised in the colon, revealing a prevailing trend of colon localisation. In a study conducted in the Algerian East, 68.9% of CRC cases were found in the colon [19]. Similarly, 65% of CRC cases were localised in the colon in the USA, which records 8.4% of the global CRC incidence [20], and a national retrospective cohort study in England identified 63.5% of colon cancer [21], while in China, which contributes to 30% of the global CRC incidence, 55.1% of all CRC cases were colon cancers [1].
In our study, 78% of diagnosed CRC patients were aged 50 years or older. This indicates that CRC incidence remains more frequent in older patients in the study population, which corroborates the trend observed globally [20, 22]. The proportion of early-onset CRC patients was similar to that found in eastern Algeria (26.7%) [19] and Saudi Arabia (25%) [23], but higher than the results reported in the US (10%) [20]. This suggests that the incidence of CRC in younger adults may be increasing in our population and that there may be other factors contributing to CRC incidence, such as environmental or genetic factors. We noticed that early-onset patients (who were below the age of 50 years) were more likely to have primary rectal cancer than colon tumours when compared to late-onset patients (aged 50 years or older) which matches the findings reported in several countries like the USA and Japan [20, 24].
Over the last decade, the incidence of rectal cancer in the United States has gradually increased among those under the age of 50, with an annual increase of around 2% [25]. Similarly, findings from a European study [26] spanning from 1990 to 2016 show varying rates of increase in rectal cancer incidence across different age groups: a 3.5% annual rise among individuals aged 20–29 years, a 1.6% increase among those aged 30–39 years, and no significant change in trend among those aged 40–49 years. In contrast, China had a modest drop in rectal cancer incidence between 2005 and 2015, regardless of age at diagnosis, but was prominently expressed within the 35–49 age group seeing a 1.6% fall [27].
Algeria has experienced a significant shift in its disease burden, transitioning from a predominance of infectious diseases to the dominance of chronic non-communicable diseases (NCDs) as the leading cause of mortality. The country has made significant progress in improving living conditions and developing a free public health security system supported by the government [28]. While Algeria has an extensive and relatively comprehensive social security system, which includes several programs that target a wide range of vulnerable groups, there is room for all programs to improve in terms of coverage and adequacy of benefits [29]. The epidemiological transition has led to a high prevalence of NCDs, including diabetes, obesity, cardiovascular diseases and hypertension. According to the International Diabetes Federation [30], the relative prevalence of diabetes in Algeria was 7.1% in the age group of 20–79 years in 2021. Furthermore, according to Algeria’s STEPS survey from 2016 to 2017 [31], the rate of obesity ranges between 14.1% in men and 30.1% in women (21.8% for both sexes), and the proportion of high blood pressure was 31.6% [32].
Furthermore, in our study, the most frequent associated factors with CRC were hypertension, diabetes, appendectomy and family history of cancer. Compared to individuals with normotension, Zhang et al [8] found in a meta-analysis that individuals with hypertension had an increased CRC risk. The same trend was observed in a large study conducted by Kaneko et al [33], which revealed that elevated systolic and diastolic blood pressure levels were linked to a higher risk of incident CRC highlighting therefore the importance of supervising blood pressure to identify individuals at higher risk of developing CRC. Although the specific mechanisms underlying the link between hypertension and CRC remain unknown, these findings indicate a correlation that merits further investigation. Diabetes prevalence was associated with an increased risk of all CRC types [5, 8]. One reason that can explain this relationship is the shared risk factors between both conditions such as dietary and genetic factors. Another explanation could be that both conditions share molecular and cellular pathways, for instance, epithelial cell injury, inflammatory responses` activation and Wnt/β-catenin pathways [34].
The following studies attempted to investigate the correlation between a family history of all cancers and CRC risk yielding conflicting results. In a meta-analysis performed by Far et al [35], a positive first-degree family history of CRC showed an 87% statistically significant increase in CRC risk (RR = 1.87; 95% CI = 1.68, 2.09). As shown in a case-control study conducted by Negrichi and Taleb [36] in eastern Algeria, a family history of cancer in one of the first-degree relatives showed a significant relationship with the risk of developing CRC (OR = 2.46; 95% CI = 1.50, 4.05; p < 0.001), however, a more recent investigation by Lewandowska et al [6] did not find a significant association, which may indicate that other factors, such as genetic polymorphisms, lifestyle, and dietary habits, could also play a role in CRC predisposition. These contrasting findings suggest that the association between family history, which is already an established risk factor for CRC and included in several screening guidelines and risk prediction models, and the risk of CRC may be complex and requires further examination.
Several studies have investigated the relationship between appendectomy and CRC risk, with some showing an increased risk of CRC after appendectomy, while others have either found no association or a potential protective effect. In a meta-analysis, individuals who had experienced an appendectomy had an elevated risk of CRC, implying a possible link with CRC development [7]. Conversely, a 14 years of follow-up large retrospective cohort study found that appendectomy patients had a 1.14 times higher risk of developing CRC than the general population [37]. However, the increased risk was observed in another study, and it was primarily noticed in the first year after the appendectomy which may represent a potential bias. No statistically significant correlation was identified between appendectomy and the risk of CRC after adjusting for an appropriate delay period after surgery [38]. Recently, a study by Rothwell et al [39] reported an inverse relationship between undergoing appendectomy and the risk of colon cancer. Although there was a 9% reduction in CRC risk associated with appendectomy, it did not result in a lower overall CRC risk (HR = 0.91; 95% CI = 0.79, 1.02). The complex interplay between appendectomy, gut microbiota changes, inflammation, and CRC risk warrants further investigation to clarify the precise nature of this relationship and potential clinical implications.
Lifestyle changes, particularly in urban areas, have resulted in an unhealthy diet consisting of processed and high-fat foods. A Westernized diet, which is rich in red and processed meats, refined sugars, and saturated fats has replaced the traditional Algerian diet, rich in fruits, vegetables, and lean meats. This shift, combined with sedentary lifestyles and lack of physical activity, has been linked to an increased risk of CRC [36].
Furthermore, the Algerian National Cancer Screening Committee introduced CRC screening into the national cancer plan after the 2015–2019 program overlooked it. This decision followed the publication of results from the National Cancer Registry Network in January 2017, highlighting the significant incidence of CRC. Pilot studies using immunological tests were launched in three regions: Bejaia, Annaba and Batna. These tests aim to detect blood in the stool. Despite a modest overall participation rate of 26%, the rate rose to 98% among those with positive test results. A lack of awareness and screening programs has contributed to the late detection of CRC cases in Algeria. Unlike some Western countries, where routine screenings and awareness campaigns are common, Algeria lacks a comprehensive nationwide screening program. As a result, many cases are diagnosed at advanced stages, reducing the chances of successful treatment and survival [40, 41].
The current study results could significantly contribute to the development of a comprehensive approach to CRC prevention, diagnosis and treatment in Algeria. It offers insights into age-specific patterns, sex-based differences, and anatomic sites, which could enhance our understanding of CRC in this specific region. Public health interventions aimed at increasing awareness of CRC, supporting healthy dietary practices, and mitigating exposure to risk factors may benefit the population.
Certain limitations may affect the study’s results, including potential biases associated with retrospective data collection, the single-centre nature of the study, the small population number, and missing information in medical records for some variables which could potentially affect the generalisability of these findings.
Conclusion
CRC incidence rates are increasing in Algeria. This retrospective study demonstrates the current state of CRC incidence in the northwest region of the country. Moreover, the study findings provide valuable data for healthcare planning and resource allocation which include ensuring access to screening services, diagnostic tools, treatment facilities, and supportive care for CRC patients to address the needs of the population.
List of abbreviations
BMI, Body mass index; BRAF, B-Raf Proto-Oncogene, Serine/Threonine Kinase; CA 19-9, Carbohydrate antigen 19-9; CEA, carcinoembryonic antigen; CI, Confidence interval; CRC, colorectal cancer; GLOBOCAN, Global cancer observatory; HR, Hazard ratio; NCD, non-communicable disease; NRAS, Neuroblastoma; RAS; OR, odds ratio; RR, Relative risk.
Acknowledgments
We extend our appreciation to the personnel of the anti-cancer centre of Sidi Bel Abbes for their assistance and support during the study.
Conflicts of interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Funding
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Author contributions
SE conceptualisation, data curation, formal analysis, investigation, methodology, visualisation, writing – original draft, writing – review & editing. SM supervision, validation. DE conceptualisation, data curation, investigation, methodology. DY conceptualisation, methodology, project administration, resources, supervision, validation. MBK supervision, validation, writing – review & editing.
References
1. Ferlay J, Ervik M, and Lam F, et al (2020) Global Cancer Observatory: Cancer Today [Internet] [https://gco.iarc.fr/today] Lyon, France International Agency for Research on Cancer Date accessed: 19/07/23
2. Arhin N, Ssentongo P, and Taylor M, et al (2022) Age-standardised incidence rate and epidemiology of colorectal cancer in Africa: a systematic review and meta-analysis BMJ Open 12(1) e052376 https://doi.org/10.1136/bmjopen-2021-052376 PMID: 35039287 PMCID: 8765019
3. AlZaabi A (2022) Colorectal cancer in the Arab world Cancer in the Arab world eds HO Al-Shamsi, IH Abu-Gheida, F Iqbal, and A Al-Awadhi (Singapore: Springer) pp 363–379 https://doi.org/10.1007/978-981-16-7945-2_23
4. Awedew AF, Asefa Z, and Belay WB (2022) Burden and trend of colorectal cancer in 54 countries of Africa 2010–2019: a systematic examination for global burden of disease BMC Gastroenterol 22(1) https://doi.org/10.1186/s12876-022-02275-0 PMID: 35468750 PMCID: 9036749
5. Demb J, Earles A, and Martínez ME, et al (2019) Risk factors for colorectal cancer significantly vary by anatomic site BMJ Open Gastroenterol 6(1) e000313 https://doi.org/10.1136/bmjgast-2019-000313 PMID: 31523441 PMCID: 6711437
6. Lewandowska A, Rudzki G, and Lewandowski T, et al (2022) Risk factors for the diagnosis of colorectal cancer Cancer Control 29 10732748211056692 https://doi.org/10.1177/10732748211056692 PMID: 35000418 PMCID: 8753079
7. Liu Z, Ma X, and Zhu C, et al (2023) Risk of colorectal cancer after appendectomy: a systematic review and meta-analysis J Gastroenterol Hepatol 38(3) 350–358 https://doi.org/10.1111/jgh.16108 PMID: 36637673
8. Zhang C, Cheng Y, and Luo D, et al (2021) Association between cardiovascular risk factors and colorectal cancer: a systematic review and meta-analysis of prospective cohort studies eClinicalMedicine 34 https://doi.org/10.1016/j.eclinm.2021.100794 PMID: 33997727 PMCID: 8102710
9. Cardoso R, Guo F, and Heisser T, et al (2021) Colorectal cancer incidence, mortality, and stage distribution in European countries in the colorectal cancer screening era: an international population-based study Lancet Oncol 22(7)1002–1013 https://doi.org/10.1016/S1470-2045(21)00199-6 PMID: 34048685
10. Siegel RL, Miller KD, and Fuchs HE, et al (2022) Cancer statistics, 2022 CA Cancer J Clin 72(1) 7–33 https://doi.org/10.3322/caac.21708 PMID: 35020204
11. Sung H, Ferlay J, and 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 PMID: 33538338
12. Centers for Disease Control and Prevention (2022) All About Adult BMI [Internet] (Atlanta: CDC) [https://www.cdc.gov/healthyweight/assessing/bmi/adult_bmi/index.html] Date accessed: 20/07/23
13. World Health Organization (2016) International Statistical Classification of Diseases and Related Health Problems 10th edn (Geneva: World Health Organization)
14. Amin MB, Edge SB, and Greene FL, et al (2017) AJCC Cancer Staging Manual 8th edn (Cham: Springer)
15. Li ZN, Zhao L, and Yu LF, et al (2020) BRAF and KRAS mutations in metastatic colorectal cancer: future perspectives for personalized therapy Gastroenterol Rep 8(3) 192–205 https://doi.org/10.1093/gastro/goaa022
16. Thomsen M, Skovlund E, and Sorbye H, et al (2018) Prognostic role of carcinoembryonic antigen and carbohydrate antigen 19-9 in metastatic colorectal cancer: a BRAF-mutant subset with high CA 19-9 level and poor outcome Br J Cancer 118 1609–1616 https://doi.org/10.1038/s41416-018-0115-9 PMID: 29872151 PMCID: 6008450
17. R Core Team (2023) R: A Language and Environment for Statistical Computing (Vienna: R Foundation for Statistical Computing) [https://www.R-project.org]
18. Sjoberg DD, Whiting K, and Curry M, et al (2021) Reproducible summary tables with the gtsummary package R J 13(1) 570–580 https://doi.org/10.32614/RJ-2021-053
19. Negrichi S and Taleb S (2020) Evaluation of nutritional status of colorectal cancer patients from Algerian East using anthropometric measurements and laboratory assessment Iran J Public Health 49(7) 1242–1251 PMID: 33083290 PMCID: 7548495
20. Chang SH, Patel N, and Du M, et al (2022) Trends in early-onset vs late-onset colorectal cancer incidence by race/ethnicity in the United States cancer statistics database Clin Gastroenterol Hepatol 20(6) e1365–e1377 https://doi.org/10.1016/j.cgh.2021.07.035
21. Arhi CS, Burns EM, and Bottle A, et al (2020) Delays in referral from primary care worsen survival for patients with colorectal cancer: a retrospective cohort study Br J Gen Pract 70(696) e463–e471 https://doi.org/10.3399/bjgp20X710441 PMID: 32540874 PMCID: 7299547
22. Gutlic I, Schyman T, and Lydrup ML, et al (2019) Increasing colorectal cancer incidence in individuals aged < 50 years – a population-based study Int J Colorectal Dis 34(7) 1221–1226 https://doi.org/10.1007/s00384-019-03312-3 PMID: 31102007
23. Alyabsi M, Algarni M, and Alshammari K (2021) Trends in colorectal cancer incidence rates in Saudi Arabia (2001–2016) using Saudi national registry: early- versus late-onset disease Front Oncol 11 730689 https://doi.org/10.3389/fonc.2021.730689
24. Nagai Y, Hata K, and Kawai K, et al (2016) Clinicopathological features of colorectal cancer patients under the age of 50: recent experience and case-control study of prognosis in a Japanese cohort Gastroenterologia 93(4) 272–279 https://doi.org/10.1159/000446344
25. Siegel RL, Wagle NS, and Cercek A, et al (2023) Colorectal cancer statistics, 2023 CA Cancer J Clin 73(3) 233–254 https://doi.org/10.3322/caac.21772 PMID: 36856579
26. Vuik FE, Nieuwenburg SA, and Bardou M, et al (2019) Increasing incidence of colorectal cancer in young adults in Europe over the last 25 years Gut 68(10) 1820–1826 https://doi.org/10.1136/gutjnl-2018-317592 PMID: 31097539 PMCID: 6839794
27. Wang J, Liu L, and Cai Y, et al (2021) Trends in the age-related incidence of colon and rectal cancers in China, 2005–2015 Dig Liver Dis 53(7) 908–914 https://doi.org/10.1016/j.dld.2021.01.009 PMID: 33551354
28. Mammeri A and Tebaibia A (2020) Cardiometabolic risk in Algeria: past and present Intern Emerg Med 15(4) 531–535 https://doi.org/10.1007/s11739-019-02207-z
29. Merouani, W, Messekher, H, Hamaizia, A, & Ait Belkacem, M (2023) Reforming Algeria’s social protection system. Royal Institute of International Affairs https://doi.org/10.55317/9781784135751
30. International Diabetes Federation (2021) IDF Diabetes Atlas 10th edn (Brussels: International Diabetes Federation) [https://www.diabetesatlas.org]
31. World Health Organization (Surveillance, Monitoring and Reporting (SMR)) (2017) 2016-2017 STEPS Fact Sheet Algeria (Geneva: World Health Organization) [https://www.who.int/publications/m/item/2016-2017-steps-fact-sheet-algeria]
32. Moussouni A, Sidi-yakhlef A, and Hamdaoui H, et al (2022) Prevalence and risk factors of prehypertension and hypertension in Algeria BMC Public Health 22(1) 1571 https://doi.org/10.1186/s12889-022-13942-y PMID: 35982441 PMCID: 9386961
33. Kaneko H, Yano Y, and Itoh H, et al (2021) Untreated hypertension and subsequent incidence of colorectal cancer: analysis of a nationwide epidemiological database J Am Heart Assoc 10(22) e022479 https://doi.org/10.1161/JAHA.121.022479 PMID: 34724797 PMCID: 8751953
34. González N, Prieto I, and del Puerto-Nevado L, et al (2017) 2017 update on the relationship between diabetes and colorectal cancer: epidemiology, potential molecular mechanisms and therapeutic implications Oncotarget 8 18456–18485 https://doi.org/10.18632/oncotarget.14472 PMID: 28060743 PMCID: 5392343
35. Far PM, Alshahrani A, and Yaghoobi M (2019) Quantitative risk of positive family history in developing colorectal cancer: a meta-analysis World J Gastroenterol 25(30) 4278–4291 https://doi.org/10.3748/wjg.v25.i30.4278
36. Negrichi S and Taleb S (2021) Hereditary, environmental, and dietary risk factors of colorectal cancer: a case-control study in the Algerian East Environ Sci Pollut Res 28(10) 12372–12381 https://doi.org/10.1007/s11356-020-10378-y
37. Wu SC, Chen WTL, and Muo CH, et al (2015) Association between appendectomy and subsequent colorectal cancer development: an Asian population study PLos One 10(2) e0118411 https://doi.org/10.1371/journal.pone.0118411 PMID: 25710790 PMCID: 4339380
38. Lee J, Choe S, and Park JW, et al (2018) The risk of colorectal cancer after cholecystectomy or appendectomy: a population-based cohort study in Korea J Prev Med Pub Health 51(6) 281–288 https://doi.org/10.3961/jpmph.18.105
39. Rothwell JA, Mori N, and Artaud F, et al (2022) Colorectal cancer risk following appendectomy: a pooled analysis of three large prospective cohort studies Cancer Commun 42(5) 486–489 https://doi.org/10.1002/cac2.12265
40. Bounedjar A, Melzi MA, and Idir H, et al (2022) General oncology care in Algeria Cancer in the Arab world eds HO Al-Shamsi, IH Abu-Gheida, F Iqbal, and A Al-Awadhi (Singapore: Springer) pp 15–30 https://doi.org/10.1007/978-981-16-7945-2_2
41. Kamel B and Chahira M (2018) Organized screening for colorectal cancer in Algeria: first pilot study in North Africa J Clin Oncol 36(15_suppl) e15697–e15697 https://doi.org/10.1200/JCO.2018.36.15_suppl.e15697
