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CORRESPONDENCE
Year : 2014  |  Volume : 139  |  Issue : 2  |  Page : 314-318

High frequency of young age rectal cancer in a tertiary care centre of southern Assam, North East India


1 Molecular Medicine Laboratory Department of Biotechnology Assam University; Cachar Cancer Hospital & Research Centre, Meherpur, Silchar 788 015, India
2 Molecular Medicine Laboratory Department of Biotechnology Assam University, Silchar 788 011, India
3 Cachar Cancer Hospital & Research Centre, Meherpur, Silchar 788 015, India

Date of Web Publication9-Apr-2014

Correspondence Address:
Sankar Kumar Ghosh
Molecular Medicine Laboratory Department of Biotechnology Assam University, Silchar 788 011
India
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Source of Support: None, Conflict of Interest: None


PMID: 24718409

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How to cite this article:
Laskar RS, Talukdar FR, Mondal R, Kannan R, Ghosh SK. High frequency of young age rectal cancer in a tertiary care centre of southern Assam, North East India. Indian J Med Res 2014;139:314-8

How to cite this URL:
Laskar RS, Talukdar FR, Mondal R, Kannan R, Ghosh SK. High frequency of young age rectal cancer in a tertiary care centre of southern Assam, North East India. Indian J Med Res [serial online] 2014 [cited 2019 Nov 21];139:314-8. Available from: http://www.ijmr.org.in/text.asp?2014/139/2/314/130305

Sir,

Colorectal cancer (CRC) is the third most common cancer in men and the second in women worldwide [1],[2] , with significant geographical, racial and ethnic variation in its incidence rate and pattern [3],[4] . Globally, cancer of rectum and anus constitutes more than 40 per cent of the CRC cases, and its incidence peaks between the age of 60 and 70 yr, while its occurrence in patients below 40 years is rare [5] .

The incidence of rectal cancer in India is lower than that in the western countries, and it is the tenth leading cancer in India [6] . Several individual studies on Indian and Bangladeshi patients have consistently documented a relatively high proportion of young age rectal cancer (RC), with a mean age of around 40-45 yr [7],[8],[9],[10] . Interestingly, many of the reports on young age RC or CRC in India came from West Bengal, a State in the eastern region of India [8],[9] . Both Bangladesh and West Bengal are situated in the northeast region of the Indian Subcontinent, and share similar ethnic, linguistic, dietary, cultural and social characteristics.

We examined the frequency and clinicopathological characteristics of RC patients in Southern Assam (consisting of three districts: Cachar, Karimganj and Hailakandi) in a hospital based study. Our objective was to investigate if any discrepancy regarding rectal cancer in young patients occurs in this area and also to identify the associated clinicopathological features.

All patients diagnosed with rectal carcinoma at Cachar Cancer Hospital and Research Centre (CCHRC) from January 2008 to December 2011 were included in the study. This institute is a speciality oncology centre in Cachar district, which happens to be the only oncology centre serving the entire population of Southern Assam. Demographic as well as clinicopathological data of the RC patients were collected in two phases: retrospectively, for 106 cases from the hospital registry records from 2008-2010 and 38 newly diagnosed and histologically confirmed cases were included prospectively from January to December 2011. The study protocol was approved by the ethical committee of the hospital and written consent was taken from all the prospectively enrolled patients. The patients were divided into two groups; a younger group of below 40 years of age and an older group of 40 years and above. Patient data included age, sex, ethnicity, tumour morphology, tumour stage and differentiation, carcinoembryonic antigen (CEA) levels at presentation, etc.

Tumour involvements within 15 cm from the anal verge by rectal examination, colonoscopy or MRI were considered. Tumours 0.1 - 5 cm from the anal verge were classified as low rectal tumours and all resected tumours were staged according to Union for International Cancer Control (UICC) (Tumor, Node, Metastasis) TNM classification [11] . However, no patients had past history of colonic or rectal polyps or any other malignancy and most of the patients either did not have or did not disclose any family history of cancer.

Two tailed χ[2] test or Fisher exact test was used to test the sgnificance of all categorical data and students t test for continuous data.

Among all the 144 patients under study, 70 (48.61%) were below 40 years and 74 (51.39%) were ≥40 yr of age. The mean age at presentation was 43. 4 ± 15.8 yr, the youngest patient was 14 years old. More than 80 per cent of the patients were Bengali, 7-10 per cent were Manipuri and the rest belonged to various other tribal and non-tribal groups. Of the 144 patients, 142 were diagnosed with rectal adenocarcinoma, while two patients in the ≥40 yr age group had squamous cell carcinoma. The major clinical presentations were bleeding per rectum, weight loss and anaemia, altered bowel habits, large gut obstruction and abdominal lump. The tumour characteristics of younger and older patients are summarized in [Table 1]. The younger patients had predominance of low rectal tumours, advanced T-stage, poor differentiation with mucinous and signet ring and an advanced disease stage as compared to the older patients.
Table 1: Clinicopathological features of the patients below and ≥40 yr of age (2008-2011)

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In this study, about 48 per cent of young age (below 40 yr) rectal cancer was observed, with distinct clinical and pathological characteristics. Highest proportion of RC patients was observed in the age group of 30-39 (28.4%), followed by the 50-59 age group (19.4%). As such, along the age groups of 10 yr interval from 0-70+ yr, two distinct peaks in percentage were observed and the proportion of patients decreased in the subsequent age groups [Table 2]. Corresponding figures of rectal cancers, along with mean age and standard deviation from the major hospital based cancer registries (HBCRs) of India (2004-2006) viz. Mumbai, Chennai, Banglore, Dibrugarh and Thiruvanathapuram and also the population base cancer registries (PBCRs) in India (2006-2008) viz, Bangalore Mumbai, Delhi, Chennai, Kolkata and the major PBCRs of North-east India viz, Kamrup, Dibrugarh, Mizoram and Manipur are shown in [Table 2] [6],[12] . The mean age of the patients reporting to our hospital was significantly lower (P<0.001) as compared to the overall mean age of patients reported in all the HBCRs (mean age 50.4 ± 15.1 yr) and PBCRs (mean age 54.65 ± 15.5 yr). The peak observed in the age group of 30-39 in our hospital was also significantly higher (P<0.001) than all the compared registries and was consistent for all the age group between 10-39 yr (P<0.001 for 10-19 yr, P=0.02 for 20-29 yr as compared to HBCRs and P=0.001 for both groups as compared to PBCRs). The overall percentage of patients below 40 yr was significantly higher (P<0.001) in our hospital as compared to the HBCRs and PBCRs including the North-east ones. However, there was no difference in any age group above 40 yr between our hospital, HBCRs and PBCRs, except for a comparatively lesser proportion of patients in above 70 yr group in our hospital.
Table 2: Comparison of the number of patients (n), percentage of patients (%), mean age ± SD, stratified by 10-year age groups between the patients of CCHRC (from 2008 to 2011) various Hospital Based Cancer Registries (HBCRs) from 2004 to 2006 and various Population Based Cancer Registries (PBCRs) of India (from 2006 to 2008)

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Prior studies conducted in various oncology centres and hospitals have documented a relatively higher proportion (42 to ~48%) of young age RC or CRC in West Bengal compared to the rest of India [8],[9] . In one study from a tertiary oncology centre in India, a high occurrence of below 40 yr RC was reported (~35%) and 39% of the study group comprised patients from West Bengal [7] . As West Bengal, Bangladesh and the population of Southern Assam share similar geographic, dietary and ethnic characteristics, comparable genetic susceptibility and disease characteristics are also likely.

Worldwide, studies on colorectal cancer have documented distinct differences in disease

characteristics of younger and older patients in terms of stage, grade, location of tumours and survival. The younger patients present with a more aggressive disease, are advanced in stage with unfavourable histopathological findings (mucinous and signet ring cells) [13],[14],[15],[16],[17] . Our study and also studies from other hospitals in West Bengal have documented similar findings for younger patient [7],[9] . This might be as a result of distinct molecular signatures of the younger and older patients, the younger patients being more likely to have microsatellite instability (MSI) related changes indicating towards familial predisposition like hereditary non-polyposis colorectal cancer (HNPCC) [14] . In many of the reports on young age CRC from the developed countries, a positive family history was observed in 25-35 per cent of the patients [13],[16],[17] . However, in most of the studies on Indian and Bangladeshi patients and also in the patients of our population a positive family history was very rare (<1%), if at all reported [6],[7],[8],[9] . In one study conducted in UK [10] , distinct differences were observed between gene expression profiles of Bangladeshi CRC patients (61% below 40 yr) and their western counterparts. However the MSI status was similar for both the groups (16% vs. 15% MSI positive) [10] . This triggers a suspicion of underlying genetic factors associated with RC at a younger age in this population, which might be different from the already known familial cancer of large bowel like HNPCC or familial adenomatous polyposis (FAP). Further, the role of non-environmental factors is indicated by the fact that incidence of CRC in Indians and Bangladeshis migrated to western countries is much lower than the local population [18] .

In conclusion, the current study has documented a high proportion of young age rectal cancer in a hospital based study from Southern Assam and identified distinct clinicopathological differences with the older patients. As there are no routine screening programmes available for RC in this area, clinicians should give more emphasis on rectal examination by sigmodoscopy or colonoscopy in younger patients with rectal symptoms. Detailed epidemiological and molecular studies need to be done to identify the aetiology of young age rectal cancer in this region.

 
   References Top

1.GLOBOCAN 2008. Cancer Incidence and Mortality Worldwide. Lyon, France: International Agency for Research on Cancer. 2010. Available from: http://globocan.iarc.fr, accessed on October 14, 2011.  Back to cited text no. 1
    
2.Curado MP, Edwards B, Shin HR, Storm H, Ferlay J, Heanue M, et al. Cancer incidence in five continents, vol. IX. IARC Scientific Publication No.160. Lyon, France: International Agency for Research on Cancer; 2007.   Back to cited text no. 2
    
3.Center MM, Jemal A, Smith RA, Ward E. Worldwide variations in colorectal cancer. CA Cancer J Clin 2009; 59 : 366-78.  Back to cited text no. 3
    
4.Center MM, Jemal A, Ward E. International trends in colorectal cancer incidence rates. Cancer Epidemiol Biomarkers Prev 2009; 18 : 1688-94.  Back to cited text no. 4
    
5.Virk R, Gill S, Yoshida E, Radley S, Salh B. Racial differences in the incidence of colorectal cancer. Can J Gastroenterol 2010; 2 : 47-51.   Back to cited text no. 5
    
6.Three-years report of Population Based Cancer Registries 2006-2008 (Detailed Tabulations of Individual Registries Data). National Cancer Registry Programme (Indian Council of Medical Research), Bangalore November 2010. Available from: http://www.PBCR_2006_2008.aspx, accessed on December 27, 2012.  Back to cited text no. 6
    
7.Nath J, Wigley C, Keighley MR, Perakath B. Rectal cancer in young adults: a series of 102 patients at a tertiary care centre in India. Colorectal Dis 2009; 11 : 475-9.  Back to cited text no. 7
    
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9.Gupta S, Bhattacharya D, Acharya AN, Majumdar S, Ranjan P, Das S. Colorectal carcinoma in young adults: a retrospective study on Indian patients: 2000-2008. Colorectal Dis 2010; 12 : e182-9.  Back to cited text no. 9
    
10.Ahmed S, Banerjea A, Hands RE, Bustin S, Dorudi S. Microarray profiling of colorectal cancer in Bangladeshi patients. Colorectal Dis 2005; 7 : 571-5.  Back to cited text no. 10
    
11.Sobin LH, Fleming ID. TNM classification of malignant tumors, fifth edition (1997). Cancer 1997; 80 : 1803-4.   Back to cited text no. 11
    
12.Consolidated Report of Hospital Based Cancer Registries 2004-2006 (Detailed Tabulations of Individual Registries Data). National Cancer Registry Programme (Indian Council of Medical Research), Bangalore;. 2009. Available from: http://ncrpindia.org/HBLR_2004_2006/Preliminary_Pages_HBCR_Report_2004_06.pdf, accessed on December 27, 2012.  Back to cited text no. 12
    
13.Turkiewicz D, Miller B, Schache D, Cohen J, Theile D. Young patients with colorectal cancer: how do they fare? ANZ J Surg 2001; 71 : 707-10.  Back to cited text no. 13
    
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15.McMillan DC, McArdle CS. The impact of young age on cancer-specific and non-cancer-related survival after surgery for colorectal cancer: 10-year follow-up. Br J Cancer 2009; 101 : 557-60.  Back to cited text no. 15
    
16.Makela JT, Kiviniemi H. Clinicopathological features of colorectal cancer in patients under 40 years of age. Int J Colorectal Dis 2010; 25 : 823-8.  Back to cited text no. 16
    
17.Al-Barrak J, Gill S. Presentation and outcomes of patients aged 30 years and younger with colorectal cancer: a 20-year retrospective review. Med Oncol 2011; 28 : 1058-61.  Back to cited text no. 17
    
18.Winter H, Cheng KK, Cummins C, Maric R, Silcocks P, Varghese C. Cancer incidence in the south Asian population of England (1990-92). Br J Cancer 1999; 79 : 645-54.  Back to cited text no. 18
    



 
 
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