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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">MI</journal-id>
<journal-title-group>
<journal-title>Medicine International</journal-title>
</journal-title-group>
<issn pub-type="ppub">2632-2900</issn>
<issn pub-type="epub">2632-2919</issn>
<publisher>
<publisher-name>D.A. Spandidos</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">MI-1-4-00010</article-id>
<article-id pub-id-type="doi">10.3892/mi.2021.10</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Articles</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Epidemiology of neoplastic colorectal polyps in a Caribbean country</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Cawich</surname><given-names>Shamir O.</given-names></name>
<xref rid="af1-mi-1-4-00010" ref-type="aff">1</xref>
<xref rid="c1-mi-1-4-00010" ref-type="corresp"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Mahabir</surname><given-names>Avidesh</given-names></name>
<xref rid="af1-mi-1-4-00010" ref-type="aff">1</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Arthurs</surname><given-names>Milton</given-names></name>
<xref rid="af2-mi-1-4-00010" ref-type="aff">2</xref>
</contrib>
</contrib-group>
<aff id="af1-mi-1-4-00010"><label>1</label>Department of Clinical Surgical Sciences, University of the West Indies, St. Augustine Campus, St. Augustine, Trinidad and Tobago</aff>
<aff id="af2-mi-1-4-00010"><label>2</label>Department of Medicine, University of The West Indies, Mona Campus, Kingston, Jamaica</aff>
<author-notes>
<corresp id="c1-mi-1-4-00010"><italic>Correspondence to:</italic> Professor Shamir O. Cawich, Department of Clinical Surgical Sciences, University of The West Indies, St. Augustine Campus, St. Augustine, Trinidad and Tobago <email>socawich@hotmail.com</email></corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>09</month>
<year>2021</year></pub-date>
<pub-date pub-type="epub">
<day>29</day>
<month>07</month>
<year>2021</year></pub-date>
<volume>1</volume>
<issue>4</issue>
<elocation-id>10</elocation-id>
<history>
<date date-type="received">
<day>21</day>
<month>05</month>
<year>2021</year>
</date>
<date date-type="accepted">
<day>27</day>
<month>07</month>
<year>2021</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright: &#x00A9; Cawich et al.</copyright-statement>
<copyright-year>2020</copyright-year>
<license license-type="open-access">
<license-p>This is an open access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by-nc-nd/4.0/">Creative Commons Attribution-NonCommercial-NoDerivs License</ext-link>, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.</license-p></license>
</permissions>
<abstract>
<p>Screening is practiced to identify and remove neoplastic colorectal polyps prior to their transformation into colorectal cancer (CRC). The aim of the present study was to document the epidemiology of neoplastic colorectal polyps in order to obtain important data that may then be used to guide screening protocols in Jamaica. For this purpose, an audit was performed to identify all consecutive patients who had neoplastic polyps detected at a screening colonoscopy at a facility in Jamaica from January 1, 2015 to December 30, 2018. The following data were collected: Patient demographics, polyp location, polyp synchronicity and histopathological information. The results revealed that a total of 480 colonoscopies were performed over the study period. With the exclusion of 2 patients with innumerable polyps as a part of polyposis syndrome, there were a total of 92 neoplastic polyps in 68 patients. Polyps were most commonly located in the right colon (55.6&#x0025;), followed by the left colon (38&#x0025;) and rectum (6.5&#x0025;). Upon the histological evaluation, 63 polyps were found to be benign adenomas with mild to moderate dysplastic alterations, 15 were adenomas with severe dysplasia and/or carcinoma <italic>in situ</italic> and 14 had foci of invasive carcinomas. On the whole, the present study demonstrates that &#x007E;15&#x0025; of the patients screened had neoplastic polyps that were recognized as precursor lesions for CRC. The majority of these were in the right colon. These results support the call for policy makers to institute national CRC screening programs, such as the National Comprehensive Cancer Network harmonized guidelines for the Caribbean.</p>
</abstract>
<kwd-group>
<kwd>cancer</kwd>
<kwd>colorectal</kwd>
<kwd>polyps</kwd>
<kwd>Caribbean</kwd>
<kwd>demographic</kwd>
</kwd-group>
<funding-group>
<funding-statement><bold>Funding:</bold> No funding was received.</funding-statement>
</funding-group>
</article-meta>
</front>
<body>
<sec sec-type="intro">
<title>Introduction</title>
<p>There is a well-documented association between neoplastic polyps and colorectal cancer (CRC) in the adenoma-carcinoma sequence (<xref rid="b1-mi-1-4-00010" ref-type="bibr">1</xref>,<xref rid="b2-mi-1-4-00010" ref-type="bibr">2</xref>). Therefore, the majority of authorities recommend screening to identify and remove neoplastic polyps prior to their transformation into invasive CRC (<xref rid="b3-mi-1-4-00010 b4-mi-1-4-00010 b5-mi-1-4-00010 b6-mi-1-4-00010 b7-mi-1-4-00010" ref-type="bibr">3-7</xref>). However, the majority of Caribbean countries still do not have policies in place for universal CRC screening. This is largely due to the lack of prioritization by policy makers, resource limitations in the underfunded healthcare systems and a paucity of regional data to support CRC screening (<xref rid="b8-mi-1-4-00010" ref-type="bibr">8</xref>).</p>
<p>The present study thus aimed to document the epidemiology of neoplastic colorectal polyps and to obtain important data that may be used to guide screening protocols in Jamaica. To the best of our knowledge, there has been no prior report on the distribution or prevalence of neoplastic colorectal polyps in the Jamaican population.</p>
</sec>
<sec sec-type="Patients|methods">
<title>Patients and methods</title>
<sec>
<title/>
<sec>
<title>Patient information</title>
<p>After securing permission from the University of the West Indies Institutional Review Board (SA.1030/06/2021), a retrospective audit of hospital records was performed to identify all consecutive patients who underwent screening colonoscopy at the University Hospital of the West Indies in Kingston, Jamaica between January, 1, 2015 and December 30, 2018. Patient consent was waived by the local institutional review board. Only patients who underwent screening colonoscopies were included in the final study population. Patients who had colonoscopies for gastrointestinal-related symptomatology and those who had received procedures by trainee endoscopists were excluded from the study population. Patients who had polyps identified at colonoscopy were selected for further analysis. Patients with non-neoplastic polyps and those with incomplete clinical records were excluded from the study.</p>
<p>The hospital records of the patients were retrieved and the following data were extracted: Patient demographics, polyp location, polyp synchronicity and histopathological data.</p>
</sec>
</sec>
</sec>
<sec sec-type="Results">
<title>Results</title>
<p>There were 480 colonoscopies performed over the study period using an Olympus 160 series colonoscope (Olympus Corporation). A standardized bowel preparation technique was used that included clear fluids for 12 h, three sachets of PicoPrep<sup>&#x00AE;</sup> (sodium picosulphate) at 6-h intervals and two Dulcolax (Bisacodyl) tablets 6 h prior to the colonoscopy.</p>
<p>These screening colonoscopies were all performed by expert gastroenterologists who were trained in accredited post-graduate fellowship programs. The caecum was intubated in 456 (95&#x0025;) cases and no complications were recorded in these cases.</p>
<p>These patients were deemed average-risk undergoing screening. There was a family history of colorectal carcinoma in a first degree relative in 11 (2.3&#x0025;) patients, a history of inflammatory bowel disease in 2 (0.4&#x0025;) patients and none with a past personal history of malignancies, lynch syndrome or familial adenomatous polyposis coli (0&#x0025;).</p>
<p>Of the total of 480 colonoscopies, 395 patients without polyps and 15 patients with non-neoplastic polyps were excluded from further analysis, leaving a total of 70 patients with neoplastic polyps in the study population. The clinicopathological features of the patients included in the study are presented in <xref rid="tI-mi-1-4-00010" ref-type="table">Table I</xref>. These patients were of Afro-Caribbean (n=67), Caucasian (n=2) and Chinese (n=1) ethnicity. There were 37 males and 33 females with a mean age of 65.9 years (range, 29-88; median, 65; SD, &#x00B1;11.65). A representation of the patient demographics by age is presented in <xref rid="f1-mi-1-4-00010" ref-type="fig">Fig. 1</xref>.</p>
<p>In total, 45 patients had a solitary polyp and synchronous polyps were present in 25 patients: 22 patients had 2 polyps, 1 patient had 3 polyps and there were two females in the study with multiple polyps throughout the colon as a part of a polyposis syndrome. The number of polyps in the 2 patients with polyposis syndrome could not be counted accurately; thus, they were excluded from further analysis. This left a total number of 92 neoplastic polyps in 68 patients as the final study population.</p>
<p>The distribution of neoplastic polyps throughout the colon in these patients is illustrated in <xref rid="f2-mi-1-4-00010" ref-type="fig">Fig. 2</xref>. The most common location was the right side (55.6&#x0025;), followed by left-sided lesions (38&#x0025;) and then the rectum (6.5&#x0025;). Upon the histological evaluation, 63 polyps were found to be benign adenomas with mild to moderate dysplastic alterations and 23 of these had a villous morphology. These polyps had a mean size of 1.02&#x00B1;0.85 cm. There were 15 adenomas with high-grade dysplasia, 10 of which had a villous morphology. These 15 adenomas had a mean size of 1.8&#x00B1;1.28 cm. In total, 14 polyps had foci of invasive carcinomas and all 14 had a villous morphology. These polyps were larger in size with a mean diameter of 2.57&#x00B1;0.61 cm. The distribution of neoplastic polyps according to their histological evaluation is presented in <xref rid="tII-mi-1-4-00010" ref-type="table">Table II</xref>.</p>
</sec>
<sec sec-type="Discussion">
<title>Discussion</title>
<p>The majority of authorities recommend CRC screening to detect neoplastic polyps when there is still an opportunity for polypectomy prior to their progression into invasive cancer (<xref rid="b3-mi-1-4-00010 b4-mi-1-4-00010 b5-mi-1-4-00010 b6-mi-1-4-00010 b7-mi-1-4-00010" ref-type="bibr">3-7</xref>). However, there was still only opportunistic screening in Jamaica up to the year 2021, despite an estimated incidence of CRC of 12 per 100,000 individuals in the population (<xref rid="b8-mi-1-4-00010" ref-type="bibr">8</xref>).</p>
<p>Previous studies have documented a &#x2018;right shift&#x2019; in the Jamaican population (<xref rid="b8-mi-1-4-00010 b9-mi-1-4-00010 b10-mi-1-4-00010" ref-type="bibr">8-10</xref>) and in other Caribbean territories (<xref rid="b11-mi-1-4-00010 b12-mi-1-4-00010 b13-mi-1-4-00010" ref-type="bibr">11-13</xref>), where CRC primaries have become more prevalent in the right colon. Therefore, it was predictable that the precursor neoplastic polyps were most prevalent in the right colon in the present study. This is a change in disease distribution compared to studies from the 20th century, where CRC was predominantly left-sided (<xref rid="b14-mi-1-4-00010" ref-type="bibr">14</xref>,<xref rid="b15-mi-1-4-00010" ref-type="bibr">15</xref>). In that era, some experts advocated sigmoidoscopy for screening. However, it is clear that a colonoscopy is required in modern screening programs, since neoplastic polyps and CRC are more common in the right colon.</p>
<p>The &#x2018;right side&#x2019; shift cannot be overemphasized as there are fundamental differences in the clinical behavior of lesions, depending on the geographical origin in the colon (<xref rid="b16-mi-1-4-00010" ref-type="bibr">16</xref>). Right-sided CRCs have a high association with microsatellite instability and tend to present late, with non-specific symptoms (<xref rid="b13-mi-1-4-00010" ref-type="bibr">13</xref>), a higher cancer-related mortality rate (<xref rid="b18-mi-1-4-00010 b19-mi-1-4-00010 b20-mi-1-4-00010" ref-type="bibr">18-20</xref>) and worse overall survival statistics (<xref rid="b17-mi-1-4-00010" ref-type="bibr">17</xref>,<xref rid="b20-mi-1-4-00010" ref-type="bibr">20</xref>).</p>
<p>It was not surprising that the present study found a male predominance for neoplastic polyps (1.1:1) as previous studies have reported a predominance for invasive CRC among males (<xref rid="b11-mi-1-4-00010" ref-type="bibr">11</xref>,<xref rid="b13-mi-1-4-00010" ref-type="bibr">13</xref>,<xref rid="b21-mi-1-4-00010" ref-type="bibr">21</xref>). The demographic distribution was also predictable with a peak in the 6th to 8th decades of life. This matches the age distribution for invasive CRC in the Caribbean literature (<xref rid="b8-mi-1-4-00010 b9-mi-1-4-00010 b10-mi-1-4-00010 b11-mi-1-4-00010 b12-mi-1-4-00010 b13-mi-1-4-00010" ref-type="bibr">8-13</xref>). However, it is notable that 7&#x0025; of patients with neoplastic polyps were &#x003C;49 years of age. In the possibility that the traditional recommendations for screening had commenced at the age of 50 years (<xref rid="b4-mi-1-4-00010" ref-type="bibr">4</xref>) had been followed, these polyps would have been missed (two of which had already undergone malignant alterations), as these polyps had evidently been formed at an earlier age. This was slightly lower than similar data reported from Barbados, where 10.3&#x0025; of CRC diagnoses were made in individuals &#x003C;49 years of age (<xref rid="b13-mi-1-4-00010" ref-type="bibr">13</xref>). These data lend support to the updated recommendations for CRC screening to begin at the age of 45 years in the Caribbean population (<xref rid="b5-mi-1-4-00010" ref-type="bibr">5</xref>). These are important data as there is an established association between a young age at diagnosis and aggressive disease, a higher CRC stage (<xref rid="b22-mi-1-4-00010" ref-type="bibr">22</xref>) and lower survival rates (<xref rid="b17-mi-1-4-00010" ref-type="bibr">17</xref>,<xref rid="b22-mi-1-4-00010" ref-type="bibr">22</xref>). Although it is only a small proportion of the overall study group, it is still an important public health message that 7&#x0025; of Jamaicans with precursor neoplastic polyps will be &#x003C;49 years of age.</p>
<p>It should be noted that 96&#x0025; of the patients in the present study were of Afro-Caribbean ethnicity. This was expected, since the matriline of the Jamaican population is almost entirely of West African descent (<xref rid="b23-mi-1-4-00010" ref-type="bibr">23</xref>). It is well-established that when individuals from the African diaspora develop CRC, they have a more aggressive tumor biology (<xref rid="b17-mi-1-4-00010" ref-type="bibr">17</xref>,<xref rid="b22-mi-1-4-00010" ref-type="bibr">22</xref>,<xref rid="b24-mi-1-4-00010" ref-type="bibr">24</xref>,<xref rid="b25-mi-1-4-00010" ref-type="bibr">25</xref>), a greater association with KRAS mutations (<xref rid="b17-mi-1-4-00010" ref-type="bibr">17</xref>,<xref rid="b26-mi-1-4-00010" ref-type="bibr">26</xref>) and an increased cancer-related mortality (<xref rid="b22-mi-1-4-00010" ref-type="bibr">22</xref>,<xref rid="b24-mi-1-4-00010" ref-type="bibr">24</xref>). There is still an ongoing debate on whether these differences are due to a lack of screening, oncology care access inequities, socioeconomic factors or genuine differences in tumor biology; however, the fact that this is a predominantly Afro-Caribbean population must be recognized.</p>
<p>The present study documented the epidemiology of neoplastic colorectal polyps and demonstrated that these precursor lesions for CRC were identified in 15&#x0025; of individuals who underwent colonoscopies. It is considered that these results will lend support to the call for policy makers to implement national screening protocols (<xref rid="b3-mi-1-4-00010" ref-type="bibr">3</xref>,<xref rid="b5-mi-1-4-00010" ref-type="bibr">5</xref>). In the year 2018, the Caribbean Association of Hematology Oncology facilitated a consensus meeting of Caribbean experts to create guidelines for CRC tailored to the Caribbean environment. These guidelines were endorsed by the National Comprehensive Cancer Network (NCCN) in the NCCN Harmonized Guidelines for the Caribbean (<xref rid="b5-mi-1-4-00010" ref-type="bibr">5</xref>). Thus, perhaps the time has come for Jamaican policy makers to implement these protocols.</p>
<p>In conclusion, the present study demonstrated that &#x007E;15&#x0025; of individuals who underwent colonoscopies had neoplastic polyps that were as recognized precursor lesions for CRC. There is also a predominance in right-sided polyps, with 56&#x0025; of neoplastic colorectal polyps being found in the right colon. These results support the call for policy makers to institute national CRC screening programs, such as the NCCN harmonized guidelines for the Caribbean.</p>
</sec>
</body>
<back>
<ack>
<title>Acknowledgements</title>
<p>Not applicable.</p>
</ack>
<sec sec-type="data-availability">
<title>Availability of data and materials</title>
<p>The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.</p>
</sec>
<sec>
<title>Authors&#x0027; contributions</title>
<p>SOC, MA and AM conceptualized and designed the study. AM and MA collected the data and carried out the literature search. SOC, AM and MA analyzed the data. SOC prepared the manuscript. MA, AM and SOC edited the manuscript and approved the academic/intellectual content within the final version. All authors have read and approved the final manuscript. SOC, MA and AM confirm the authenticity of the data.</p>
</sec>
<sec>
<title>Ethics approval and consent to participate</title>
<p>In the present retrospective study, patient data were obtained after securing permission from the University of the West Indies Review Board (SA.1030/06/2021).</p>
</sec>
<sec>
<title>Patient consent for publication</title>
<p>Not applicable.</p>
</sec>
<sec sec-type="COI-statement">
<title>Competing interests</title>
<p>The authors declare that they have no competing interests.</p>
</sec>
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</back>
<floats-group>
<fig id="f1-mi-1-4-00010" position="float">
<label>Figure 1</label>
<caption><p>Distribution of patients with neoplastic polyps by patient age.</p></caption>
<graphic xlink:href="mi-01-04-00010-g00.tif" />
</fig>
<fig id="f2-mi-1-4-00010" position="float">
<label>Figure 2</label>
<caption><p>Distribution of neoplastic polyps throughout the colon and rectum. Red circles indicate the number of polyps in the right colon, yellow circles indicate the number of polyps in the left colon and the green circles indicates the number of polyps in the rectum.</p></caption>
<graphic xlink:href="mi-01-04-00010-g01.tif" />
</fig>
<table-wrap id="tI-mi-1-4-00010" position="float">
<label>Table I</label>
<caption><p>Clinicopathological characteristics of the patients in the present study (n=70).</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="middle">Characteristic</th>
<th align="center" valign="middle">No. of patients</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Male</td>
<td align="center" valign="middle">37</td>
</tr>
<tr>
<td align="left" valign="middle">Female</td>
<td align="center" valign="middle">33</td>
</tr>
<tr>
<td align="left" valign="middle">Age, mean &#x00B1; SD (years)</td>
<td align="center" valign="middle">65.9&#x00B1;11.65</td>
</tr>
<tr>
<td align="left" valign="middle">1 Polyp</td>
<td align="center" valign="middle">45</td>
</tr>
<tr>
<td align="left" valign="middle">2 Polyps</td>
<td align="center" valign="middle">22</td>
</tr>
<tr>
<td align="left" valign="middle">3 Polyps</td>
<td align="center" valign="middle">1</td>
</tr>
<tr>
<td align="left" valign="middle">Numerous polyps (polyposis syndrome)</td>
<td align="center" valign="middle">2 (excluded from the final analysis)</td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="tII-mi-1-4-00010" position="float">
<label>Table II</label>
<caption><p>Histological evaluation of neoplastic polyps.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="middle">Location of polyp</th>
<th align="center" valign="middle">All patients (n=92), n (&#x0025;)</th>
<th align="center" valign="middle">No. of patients with adenomas with low/intermediate grade dysplasia</th>
<th align="center" valign="middle">No. of patients with carcinoma <italic>in situ</italic></th>
<th align="center" valign="middle">No. of patients with invasive carcinoma</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Right colon</td>
<td align="center" valign="middle">51(56)</td>
<td align="center" valign="middle">33</td>
<td align="center" valign="middle">8</td>
<td align="center" valign="middle">10</td>
</tr>
<tr>
<td align="left" valign="middle">Left colon</td>
<td align="center" valign="middle">36(39)</td>
<td align="center" valign="middle">26</td>
<td align="center" valign="middle">7</td>
<td align="center" valign="middle">3</td>
</tr>
<tr>
<td align="left" valign="middle">Rectum</td>
<td align="center" valign="middle">5(5)</td>
<td align="center" valign="middle">4</td>
<td align="center" valign="middle">0</td>
<td align="center" valign="middle">1</td>
</tr>
<tr>
<td align="left" valign="middle">Total</td>
<td align="center" valign="middle">&#x00A0;</td>
<td align="center" valign="middle">63</td>
<td align="center" valign="middle">15</td>
<td align="center" valign="middle">14</td>
</tr>
</tbody>
</table>
</table-wrap>
</floats-group>
</article>
