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<article xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" article-type="research-article" xml:lang="en">
<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">SAJO</journal-id>
<journal-title-group>
<journal-title>SA Journal of Oncology</journal-title>
</journal-title-group>
<issn pub-type="ppub">2518-8704</issn>
<publisher>
<publisher-name>AOSIS</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">SAJO-2-37</article-id>
<article-id pub-id-type="doi">10.4102/sajo.v2i0.37</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Original Research</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Epidemiological review of childhood cancers in central Sudan</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0595-5186</contrib-id>
<name>
<surname>Elhassan</surname>
<given-names>Moawia M.A.</given-names>
</name>
<xref ref-type="aff" rid="AF0001">1</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6090-7566</contrib-id>
<name>
<surname>Mohamedani</surname>
<given-names>Ahmed A.</given-names>
</name>
<xref ref-type="aff" rid="AF0002">2</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9769-1837</contrib-id>
<name>
<surname>Yousif</surname>
<given-names>Nada O.</given-names>
</name>
<xref ref-type="aff" rid="AF0001">1</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5382-7728</contrib-id>
<name>
<surname>Elhaj</surname>
<given-names>Nafessa M.</given-names>
</name>
<xref ref-type="aff" rid="AF0001">1</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6645-4895</contrib-id>
<name>
<surname>Qaddoumi</surname>
<given-names>Ibrahim</given-names>
</name>
<xref ref-type="aff" rid="AF0003">3</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7432-1611</contrib-id>
<name>
<surname>Abuidres</surname>
<given-names>Dafalla O.</given-names>
</name>
<xref ref-type="aff" rid="AF0001">1</xref>
</contrib>
<aff id="AF0001"><label>1</label>Department of Clinical Oncology, National Cancer Institute, University of Gezira, Sudan</aff>
<aff id="AF0002"><label>2</label>Department of Pathology, University of Gezira, Sudan</aff>
<aff id="AF0003"><label>3</label>Department of Global Pediatric Medicine, St. Jude Children&#x2019;s Research Hospital, United States</aff>
</contrib-group>
<author-notes>
<corresp id="cor1"><bold>Corresponding author:</bold> Moawia Elhassan, <email xlink:href="moawia2@gmail.com">moawia2@gmail.com</email></corresp>
</author-notes>
<pub-date pub-type="epub"><day>03</day><month>04</month><year>2018</year></pub-date>
<pub-date pub-type="collection"><year>2018</year></pub-date>
<volume>2</volume>
<elocation-id>37</elocation-id>
<history>
<date date-type="received"><day>27</day><month>01</month><year>2018</year></date>
<date date-type="accepted"><day>05</day><month>03</month><year>2018</year></date>
</history>
<permissions>
<copyright-statement>&#x00A9; 2018. The Authors</copyright-statement>
<copyright-year>2018</copyright-year>
<license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/">
<license-p>Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.</license-p>
</license>
</permissions>
<abstract>
<sec id="st1">
<title>Background</title>
<p>Epidemiological studies of paediatric cancer incidence in Sudan are rare.</p>
</sec>
<sec id="st2">
<title>Objectives</title>
<p>The aim of this study was to provide baseline information about the epidemiology of childhood cancers in patients treated at the National Cancer Institute (NCI) in Wad Medani, Sudan.</p>
</sec>
<sec id="st3">
<title>Methods</title>
<p>We performed a retrospective health facility&#x2013;based study of cancer incidence and patient characteristics of children who were treated at the NCI from January 1999 to December 2015. The changing patterns of cancers incidence during the study period were also recorded.</p>
</sec>
<sec id="st4">
<title>Results</title>
<p>Of 15 387 new patients with cancer who were registered at the NCI during the study period, 1159 (7.5&#x0025;) were children (younger than 15 years). The mean age of the paediatric patients was 7 years, with standard deviation of 5. Most of the patients (36&#x0025;) were 10 to 15 years old, 33&#x0025; were 0 to 4 years old and 31&#x0025; were 5 to 10 years old. Among the study population, 60&#x0025; were males and 40&#x0025; were females. Approximately 76&#x0025; of children lived in rural areas in Sudan. Leukaemias (29&#x0025;) and lymphomas (26&#x0025;) comprised 55&#x0025; of all paediatric cancers. Central nervous system (CNS) tumours constituted 6&#x0025; of all paediatric tumours, whereas non-CNS embryonal tumours (i.e. nephroblastoma, neuroblastoma, hepatoblastoma and retinoblastoma) accounted for 20&#x0025;. The average number of cases per year increased from 42 in 1999&#x2013;2005 to 75 in 2006&#x2013;2010 and 106 in 2011&#x2013;2015.</p>
</sec>
<sec id="st5">
<title>Conclusion</title>
<p>The number of patients seeking treatment for childhood cancers has increased every year in central Sudan. Leukaemias and lymphomas constitute more than half of these cancers. A population-based cancer registry is needed to determine the true incidence of childhood cancers in Sudan.</p>
</sec>
</abstract>
</article-meta>
</front>
<body>
<sec id="s0001">
<title>Introduction</title>
<p>Childhood cancers are entities distinct from those occurring in adults. They are relatively rare, comprising less than 1&#x0025; of malignant diseases.<sup><xref ref-type="bibr" rid="CIT0001">1</xref></sup> Marked differences in the incidence rates of childhood cancers are apparent in developed and developing countries.<sup><xref ref-type="bibr" rid="CIT0002">2</xref>,<xref ref-type="bibr" rid="CIT0003">3</xref></sup> Of the estimated 250 000 children in whom cancer is diagnosed every year, approximately 200 000 live in countries with limited resources.<sup><xref ref-type="bibr" rid="CIT0004">4</xref></sup> In Africa, approximately 50 000 new cases of childhood cancer are diagnosed every year.<sup><xref ref-type="bibr" rid="CIT0005">5</xref></sup></p>
<p>The frequencies at which different types of cancers occur also differ between high-income countries (HICs) and low- and middle-income countries (LMICs). Indeed, income-based variations have been observed even within the same country. The most common malignant neoplasms among children in developed countries are leukaemia and central nervous system (CNS) tumours.<sup><xref ref-type="bibr" rid="CIT0002">2</xref></sup> In Africa, CNS tumours are largely outnumbered by leukaemias and lymphomas.<sup><xref ref-type="bibr" rid="CIT0006">6</xref>,<xref ref-type="bibr" rid="CIT0007">7</xref></sup> Geographic variations in the incidence rates at which different types of childhood cancers occur may suggest that genetic or environmental factors influence disease susceptibility.<sup><xref ref-type="bibr" rid="CIT0008">8</xref></sup> In many LMICs, the low incidence of some childhood tumours (especially brain tumours) is generally the consequence of failing to diagnose.</p>
<p>In HICs, more than 80&#x0025; of children with malignant neoplasms are cured. However, most children with cancer live in LMICs, where the cure rate is much lower.<sup><xref ref-type="bibr" rid="CIT0009">9</xref></sup> Malnutrition and infectious disease, such as malaria, HIV and tuberculosis, remain the most important paediatric health problems in Africa. Consequently, childhood cancers remain a low priority on the health agendas of many African governments. Therefore, a basic epidemiological understanding of malignant diseases in children is urgently needed for optimal channelling of scarce health care resources in limited resource settings. Reports of the incidence of childhood cancers are limited in sub-Saharan Africa, and most of this information relies on hospital-based statistics. The South Africa Children Tumour Registry (SACTR) is the only paediatric cancer registry in Africa.<sup><xref ref-type="bibr" rid="CIT0010">10</xref></sup> The most extensive data on the incidence of childhood cancers in sub-Saharan Africa have been published recently. The data reported were extracted from six population-based cancer registries, which, as members of the African Cancer Registry Network, have been evaluated as achieving a reasonable degree of population coverage.<sup><xref ref-type="bibr" rid="CIT0011">11</xref></sup></p>
<p>In Sudan, where 40&#x0025; of the population is under the age of 15 years, the true incidence of childhood cancers is unknown because of the lack of a national cancer registry. Reports of the occurrence of childhood cancers in Sudan are limited. In the absence of national cancer registries, hospital registries are the only source of information for assessing disease patterns.<sup><xref ref-type="bibr" rid="CIT0012">12</xref>,<xref ref-type="bibr" rid="CIT0013">13</xref></sup> Here, we provide baseline information about the epidemiology of childhood cancers in central Sudan by reviewing hospital records of patients who were treated at the National Cancer Institute (NCI), the only cancer treating institution in central Sudan, from January 1999 to December 2015. Our findings may be generally representative of childhood cancers within the paediatric population of central Sudan.</p>
</sec>
<sec id="s0002">
<title>Methods</title>
<sec id="s20003">
<title>Setting</title>
<p>The NCI, located in the central Sudanese state of Gezira, was established in 1989 in the Gezira capital Wad Medani. The NCI began treating patients with cancer in 1999. Today, the NCI serves approximately 4 million inhabitants of Gezira and additional patients from nearby states, such as Sennar, Gadarif, Blue Nile and Kassala. These states are connected to Wad Medani by a highway that connects these states to Khartoum, the capital of Sudan. The NCI is the only cancer treatment facility in the entire region; thus, the hospital registry functions similarly to a population-based registry. The cancer treatment modalities available at the NCI include radiotherapy, chemotherapy and palliative care. A complete clinical workup (e.g. ultrasound, X-rays, blood tests, bone marrow examination, tumour marker analysis and nuclear imaging) is available at NCI. In the region, there is one Computed tomography (CT) in the government hospital and one magnetic resonance imaging (MRI) scanner available in private hospitals. Histopathologic and cytopathologic studies are provided by the University of Gezira Medical Laboratory. Surgical operations were performed at Gezira National Center for Pediatric Surgery and Gezira Center for Neurosurgery, both of which are located in Wad Medani city.</p>
</sec>
<sec id="s20004">
<title>Study design</title>
<p>We performed a retrospective health facility&#x2013;based study to characterise the incidence of children with cancers who were treated at the NCI from January 1999 (i.e. the starting date of cancer treatment at the NCI) to December 2015. We analysed data obtained from patient case folders, pathology records and radiology reports. All records were retrieved from the NCI Records Department. We investigated each case for age at diagnosis, sex, place of residence, tumour sites and morphologic or histopathologic tumour information. Cancers were classified according to the International Classification of Childhood Cancer as set forth by the World Health Organization.<sup><xref ref-type="bibr" rid="CIT0002">2</xref>,<xref ref-type="bibr" rid="CIT0014">14</xref></sup></p>
</sec>
<sec id="s20005">
<title>Statistical analysis</title>
<p>Retrieved data were recorded in precoded protocol forms specifically designed for the study and then entered into a study database. The data were analysed with the Statistical Package for the Social Sciences (SPSS) version 20 statistical package. We present statistical data as frequency and percentage for a categorical variable or as both mean &#x00B1; standard deviation (s.d.) and median (range) for a continuous variable.</p>
</sec>
<sec id="s20006">
<title>Ethical considerations</title>
<p>Ethical approval for this retrospective study was obtained from the NCI&#x2019;s ethical committee. Because of the retrospective nature of the study, the ethical committee waived the requirement of informed consent.</p>
</sec>
</sec>
<sec id="s0007">
<title>Results</title>
<p>Of 15 387 new patients with cancer registered at the NCI from January 1999 to December 2015, 1159 (7.5&#x0025;) were children (younger than 15 years). Nearly all paediatric cancers (1134; 98&#x0025;) were diagnosed according to their histopathology, although 25 were diagnosed (all brainstem tumours) on the basis of clinical evaluation and imaging. The demographic data of the paediatric cancer population revealed that the median age at diagnosis was 6 years (range, 1&#x2013;15 years). Cancers were categorised according to patient age groups as follows: 0 to 4 years, 5 to 9 years and 10 to 15 years. The distribution of children with cancer according to age group indicated that most (36&#x0025;) corresponded with the 10- to 15-year age group, followed by the 0- to 4-year (33&#x0025;) and 5- to 10-year (31&#x0025;) age groups. Of all children, 60&#x0025; were boys and 40&#x0025; were girls, with a male-to-female ratio of 1.5:1.0. Approximately 76&#x0025; of the children lived in rural areas.</p>
<p>Leukaemias were the highest frequency cancer type (29&#x0025;) followed closely by lymphomas (26&#x0025;) (<xref ref-type="table" rid="T0001">Table 1</xref>). Non-CNS embryonal tumours (i.e. nephroblastoma, neuroblastoma, hepatoblastoma and retinoblastoma) occurred in 209 cases (19&#x0025;). Among them, nephroblastoma was more frequent than neuroblastoma, retinoblastoma and hepatoblastoma. CNS tumours were the fifth (6&#x0025;) most commonly found tumours in children who were treated at the NCI during the study period. The nasopharynx region accounted for 52&#x0025; of all carcinomas diagnosis (29/55).</p>
<table-wrap id="T0001">
<label>TABLE 1</label>
<caption><p>Distribution of childhood cancers according to patient age, sex and relative frequency (<italic>n</italic> = 1159).</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th valign="top" align="left" rowspan="2">Cancer type</th>
<th valign="top" align="center" colspan="4">Number of patients<hr/></th>
<th valign="top" align="center" rowspan="2">Male-to-female ratio</th>
<th valign="top" align="center" rowspan="2">Relative frequency (&#x0025;)</th>
</tr>
<tr>
<th valign="top" align="center">0&#x2013;4 years</th>
<th valign="top" align="center">5&#x2013;9 years</th>
<th valign="top" align="center">10&#x2013;15 years</th>
<th valign="top" align="center">Total</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Leukaemias</td>
<td align="center">94</td>
<td align="center">113</td>
<td align="center">133</td>
<td align="center">340</td>
<td align="center">1.6</td>
<td align="center">29.3</td>
</tr>
<tr>
<td align="left">Lymphomas</td>
<td align="center">68</td>
<td align="center">117</td>
<td align="center">116</td>
<td align="center">301</td>
<td align="center">2.4</td>
<td align="center">26.0</td>
</tr>
<tr>
<td align="left">Central nervous system tumours</td>
<td align="center">9</td>
<td align="center">29</td>
<td align="center">33</td>
<td align="center">71</td>
<td align="center">1.6</td>
<td align="center">6.1</td>
</tr>
<tr>
<td align="left">Neuroblastoma</td>
<td align="center">34</td>
<td align="center">12</td>
<td align="center">1</td>
<td align="center">47</td>
<td align="center">1.2</td>
<td align="center">4.1</td>
</tr>
<tr>
<td align="left">Retinoblastoma</td>
<td align="center">46</td>
<td align="center">10</td>
<td align="center">0</td>
<td align="center">56</td>
<td align="center">1.2</td>
<td align="center">4.8</td>
</tr>
<tr>
<td align="left">Nephroblastoma</td>
<td align="center">71</td>
<td align="center">25</td>
<td align="center">10</td>
<td align="center">106</td>
<td align="center">0.9</td>
<td align="center">9.2</td>
</tr>
<tr>
<td align="left">Liver tumours</td>
<td align="center">7</td>
<td align="center">2</td>
<td align="center">4</td>
<td align="center">13</td>
<td align="center">1.2</td>
<td align="center">1.1</td>
</tr>
<tr>
<td align="left">Bone tumours</td>
<td align="center">1</td>
<td align="center">5</td>
<td align="center">31</td>
<td align="center">37</td>
<td align="center">0.8</td>
<td align="center">3.2</td>
</tr>
<tr>
<td align="left">Soft tissue sarcomas</td>
<td align="center">22</td>
<td align="center">26</td>
<td align="center">30</td>
<td align="center">78</td>
<td align="center">0.8</td>
<td align="center">6.7</td>
</tr>
<tr>
<td align="left">Germ cell tumours</td>
<td align="center">8</td>
<td align="center">6</td>
<td align="center">14</td>
<td align="center">28</td>
<td align="center">0.3</td>
<td align="center">2.4</td>
</tr>
<tr>
<td align="left">Carcinomas</td>
<td align="center">4</td>
<td align="center">10</td>
<td align="center">41</td>
<td align="center">55</td>
<td align="center">1.6</td>
<td align="center">4.8</td>
</tr>
<tr>
<td align="left">Other tumours</td>
<td align="center">12</td>
<td align="center">9</td>
<td align="center">6</td>
<td align="center">27</td>
<td align="center">2.9</td>
<td align="center">2.3</td>
</tr>
<tr>
<td align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td align="left"><bold>Total</bold></td>
<td align="center"><bold>376</bold></td>
<td align="center"><bold>364</bold></td>
<td align="center"><bold>419</bold></td>
<td align="center"><bold>1,159</bold></td>
<td align="center"><bold>1.5</bold></td>
<td align="center"><bold>100</bold></td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Most of these cancers occurred more commonly in boys than in girls, whereas nephroblastomas, soft tissue sarcomas, germ cell tumours and malignant bone tumours predominately occurred in female children (<xref ref-type="table" rid="T0001">Table 1</xref>).</p>
<p>When we analysed cancer type according to patient age groups, we found that leukaemias were the most frequent cancer type in the 0- to 4-year and 10- to 15-year age groups, whereas lymphomas were the most frequent in the 5- to 9-year age group (<xref ref-type="table" rid="T0001">Table 1</xref>). We observed that lymphomas, leukaemias, CNS tumours and malignant bone tumours most commonly occurred in children older than 5 years, whereas retinoblastoma, nephroblastoma and neuroblastoma occurred most commonly in children younger than 5 years. No cases of retinoblastoma were reported in the 10- to 15-year age group. Approximately 84&#x0025; of malignant bone tumours occurred in the 10- to 15-year age group. The male predominance was found in all age groups (<xref ref-type="table" rid="T0002">Table 2</xref>).</p>
<table-wrap id="T0002">
<label>TABLE 2</label>
<caption><p>Distribution of childhood cancers according to patient age group and sex (<italic>n</italic> = 1159).</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th valign="top" align="left" rowspan="2">Age group</th>
<th valign="top" align="center" colspan="5">Number of patients<hr/></th>
</tr>
<tr>
<th valign="top" align="center">Boys</th>
<th valign="top" align="center">&#x0025;</th>
<th valign="top" align="center">Girls</th>
<th valign="top" align="center">&#x0025;</th>
<th valign="top" align="center">Total</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">0&#x2013;4</td>
<td align="center">208</td>
<td align="center">55</td>
<td align="center">168</td>
<td align="center">45</td>
<td align="center">376</td>
</tr>
<tr>
<td align="left">5&#x2013;9</td>
<td align="center">230</td>
<td align="center">63</td>
<td align="center">134</td>
<td align="center">37</td>
<td align="center">364</td>
</tr>
<tr>
<td align="left">10&#x2013;15</td>
<td align="center">253</td>
<td align="center">60</td>
<td align="center">166</td>
<td align="center">40</td>
<td align="center">419</td>
</tr>
<tr>
<td align="left" colspan="6"><hr/></td>
</tr>
<tr>
<td align="left"><bold>Total</bold></td>
<td align="center"><bold>691</bold></td>
<td align="center"><bold>60</bold></td>
<td align="center"><bold>468</bold></td>
<td align="center"><bold>40</bold></td>
<td align="center"><bold>1159</bold></td>
</tr>
</tbody>
</table>
</table-wrap>
<p>To determine changes in the incidence and relative proportion of childhood cancers at the NCI over time, we categorised the number of childhood cancer cases according to three specific time periods: 1999&#x2013;2005, 2006&#x2013;2010 and 2011&#x2013;2015. The total number of childhood cancer cases increased for each subsequent time period (<xref ref-type="table" rid="T0003">Table 3</xref>). The average number of cases per year increased from 42 in 1999&#x2013;2005 to 75 in 2006&#x2013;2010 and 106 in 2011&#x2013;2015. For the 1999&#x2013;2005 period, lymphomas were the most frequent diagnoses. However, the rate of leukaemias increased and became the most common cancer type for the 2006&#x2013;2010 and 2011&#x2013;2015 periods. We also observed considerable changes in the frequency of CNS tumours and neuroblastomas over time.</p>
<table-wrap id="T0003">
<label>TABLE 3</label>
<caption><p>The number and relative frequencies of childhood cancers by period of diagnosis (<italic>n</italic> = 1159).</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th valign="top" align="left" rowspan="2">Cancer type</th>
<th valign="top" align="center" colspan="3">Period of diagnosis<hr/></th>
<th valign="top" align="center" rowspan="2">Total <italic>N</italic> (&#x0025;)</th>
</tr>
<tr>
<th valign="top" align="center">1999&#x2013;2005 <italic>n</italic> (&#x0025;)</th>
<th valign="top" align="center">2006&#x2013;2010 <italic>n</italic> (&#x0025;)</th>
<th valign="top" align="center">2011&#x2013;2015 <italic>n</italic> (&#x0025;)</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Leukaemias</td>
<td align="center">63 (24.9)</td>
<td align="center">97 (25.9)</td>
<td align="center">180 (33.9)</td>
<td align="center">340 (29.3)</td>
</tr>
<tr>
<td align="left">Lymphomas</td>
<td align="center">95 (37.5)</td>
<td align="center">96 (25.6)</td>
<td align="center">110 (20.7)</td>
<td align="center">301 (26.0)</td>
</tr>
<tr>
<td align="left">Central nervous system tumours</td>
<td align="center">5 (2.0)</td>
<td align="center">30 (8.0)</td>
<td align="center">36 (6.8)</td>
<td align="center">71 (6.1)</td>
</tr>
<tr>
<td align="left">Neuroblastoma</td>
<td align="center">0 (0.0)</td>
<td align="center">23 (6.1)</td>
<td align="center">24 (4.5)</td>
<td align="center">47 (4.1)</td>
</tr>
<tr>
<td align="left">Retinoblastoma</td>
<td align="center">7 (2.8)</td>
<td align="center">19 (5.1)</td>
<td align="center">30 (5.6)</td>
<td align="center">56 (4.8)</td>
</tr>
<tr>
<td align="left">Nephroblastoma</td>
<td align="center">32 (12.6)</td>
<td align="center">37 (9.9)</td>
<td align="center">37 (7.0)</td>
<td align="center">106 (9.2)</td>
</tr>
<tr>
<td align="left">Liver tumours</td>
<td align="center">3 (1.2)</td>
<td align="center">4 (1.1)</td>
<td align="center">6 (1.1)</td>
<td align="center">13 (1.1)</td>
</tr>
<tr>
<td align="left">Bone tumours</td>
<td align="center">11 (4.3)</td>
<td align="center">12 (3.2)</td>
<td align="center">14 (2.6)</td>
<td align="center">37 (3.2)</td>
</tr>
<tr>
<td align="left">Soft tissue sarcomas</td>
<td align="center">16 (6.3)</td>
<td align="center">21 (5.6)</td>
<td align="center">41 (7.7)</td>
<td align="center">78 (6.7)</td>
</tr>
<tr>
<td align="left">Germ cell tumours</td>
<td align="center">7 (2.8)</td>
<td align="center">8 (2.1)</td>
<td align="center">13 (2.4)</td>
<td align="center">28 (2.4)</td>
</tr>
<tr>
<td align="left">Carcinomas</td>
<td align="center">11 (4.3)</td>
<td align="center">20 (5.3)</td>
<td align="center">24 (4.5)</td>
<td align="center">55 (4.8)</td>
</tr>
<tr>
<td align="left">Other tumours</td>
<td align="center">3 (1.2)</td>
<td align="center">8 (2.1)</td>
<td align="center">16 (3.0)</td>
<td align="center">27 (2.3)</td>
</tr>
<tr>
<td align="left" colspan="5"><hr/></td>
</tr>
<tr>
<td align="left"><bold>Total</bold></td>
<td align="center"><bold>253 (100.0)</bold></td>
<td align="center"><bold>375 (100.0)</bold></td>
<td align="center"><bold>531 (100.0)</bold></td>
<td align="center"><bold>1159 (100.0)</bold></td>
</tr>
</tbody>
</table>
</table-wrap>
<p>The median age of children with cancer who lived in rural areas was 6 years and for those who lived in urban areas it was 5 years. Children from rural areas had a male-to-female ratio of 1.5, whereas those from urban areas had a male-to-female ratio of 1.3.</p>
</sec>
<sec id="s0008">
<title>Discussion</title>
<p>Childhood cancer is rare everywhere in the world, with an age-standardised annual incidence generally between 94 and 142 per million children aged 0 to 14 years. Cancer incidence in children is higher in more developed countries (113&#x2013;142 per million) than in less developed countries (85 per million).<sup><xref ref-type="bibr" rid="CIT0015">15</xref></sup> Although the source of variability between populations for some specific childhood cancer types is largely unknown, it is most likely related to exposure to risk factors.<sup><xref ref-type="bibr" rid="CIT0015">15</xref></sup> Furthermore, underreporting may contribute to a low incidence of childhood cancers in limited resource settings.<sup><xref ref-type="bibr" rid="CIT0016">16</xref></sup> In Africa, only 11&#x0025; of the population is included in a cancer-based registry.<sup><xref ref-type="bibr" rid="CIT0017">17</xref></sup></p>
<p>In Sudan, the main sources of data on childhood cancers are found in hospital-based case series.<sup><xref ref-type="bibr" rid="CIT0012">12</xref>,<xref ref-type="bibr" rid="CIT0013">13</xref>,<xref ref-type="bibr" rid="CIT0018">18</xref>,<xref ref-type="bibr" rid="CIT0019">19</xref></sup> Among all patients admitted to the NCI for treatment during the study period, children with cancers constituted 7.5&#x0025;. This finding is similar to those of a previous study in Sudan, in which childhood cancers constituted approximately 7&#x0025; of all cancer cases registered in the state of Khartoum from 2009 to 2010.<sup><xref ref-type="bibr" rid="CIT0020">20</xref></sup> This is also comparable with reports from other sub-Saharan African countries, where the proportion of childhood cancer out of all cancers varies between 1.4&#x0025; and 10&#x0025;.<sup><xref ref-type="bibr" rid="CIT0021">21</xref></sup> But the proportion of childhood cancers in this study seems to be high compared to that of HIC. Possible reasons for this difference could be that our data are from a hospital and so are not a true representation of the cancer burden. Moreover, the higher proportion of children in Sudan, as 40&#x0025; of population is under the age of 15 years (<xref ref-type="fig" rid="F0001">Figure 1</xref>), could be a possible explanation of the high number of childhood cancers.</p>
<fig id="F0001">
<label>FIGURE 1</label>
<caption><p>Population pyramid of Sudan, 2015.</p></caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="SAJO-2-37-g001.tif"/>
</fig>
<p>An interesting finding of our study is the increasing number of paediatric patients with cancer who were treated at the NCI during the study period. This is also similar with reports from other countries in Africa.<sup><xref ref-type="bibr" rid="CIT0022">22</xref>,<xref ref-type="bibr" rid="CIT0023">23</xref>,<xref ref-type="bibr" rid="CIT0024">24</xref></sup> This finding most likely reflects increased public awareness, increased awareness by general health care providers of the NCI and improved referral patterns as other centres in the region became aware of our hospital, which all contribute to the overall improved health care&#x2013;seeking behaviour of the community. This suggests that when parents are provided with the opportunity for the care they seek for their children, they will travel long distances to receive treatment from what they perceive as a high-quality cancer hospital.</p>
<p>The preponderance of boys in this study was similar to that observed in general trends in Africa and Asia<sup><xref ref-type="bibr" rid="CIT0011">11</xref>,<xref ref-type="bibr" rid="CIT0023">23</xref>,<xref ref-type="bibr" rid="CIT0025">25</xref>,<xref ref-type="bibr" rid="CIT0026">26</xref>,<xref ref-type="bibr" rid="CIT0027">27</xref>,<xref ref-type="bibr" rid="CIT0028">28</xref>,<xref ref-type="bibr" rid="CIT0029">29</xref></sup> but different from that observed in developed countries, where the male-to-female ratio is 1:1. This sex bias most likely reflects a cultural tradition of placing a higher value on boys than on girls, rather than actual increased incidence of cancer in boys.</p>
<p>The frequencies at which different types of cancers occur differ between HIC and LMICs. Comparative relative frequencies data from other LMIC countries and HIC are shown in <xref ref-type="table" rid="T0004">Table 4</xref>.<sup><xref ref-type="bibr" rid="CIT0030">30</xref>,<xref ref-type="bibr" rid="CIT0031">31</xref></sup></p>
<table-wrap id="T0004">
<label>TABLE 4</label>
<caption><p>Comparative relative frequencies data from other low- and middle-income countries countries<sup><xref ref-type="bibr" rid="CIT0010">10</xref>,<xref ref-type="bibr" rid="CIT0034">34</xref></sup> and high-income countries.<sup><xref ref-type="bibr" rid="CIT0030">30</xref>,<xref ref-type="bibr" rid="CIT0031">31</xref></sup></p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th valign="top" align="left" rowspan="2">Cancer type</th>
<th valign="top" align="center" colspan="5">Relative frequencies (&#x0025;)<hr/></th>
</tr>
<tr>
<th valign="top" align="center">United States of America</th>
<th valign="top" align="center">England</th>
<th valign="top" align="center">South Africa</th>
<th valign="top" align="center">Tanzania</th>
<th valign="top" align="center">Current study</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Leukaemias</td>
<td align="center">30.2</td>
<td align="center">29.9</td>
<td align="center">25.4</td>
<td align="center">15.0</td>
<td align="center">29.3</td>
</tr>
<tr>
<td align="left">Lymphomas</td>
<td align="center">10.9</td>
<td align="center">10.7</td>
<td align="center">13.5</td>
<td align="center">35.0</td>
<td align="center">26.0</td>
</tr>
<tr>
<td align="left">Central nervous system tumours</td>
<td align="center">21.0</td>
<td align="center">24.9</td>
<td align="center">13.4</td>
<td align="center">0.0</td>
<td align="center">6.1</td>
</tr>
<tr>
<td align="left">Neuroblastoma</td>
<td align="center">8.2</td>
<td align="center">5.9</td>
<td align="center">5.4</td>
<td align="center">1.0</td>
<td align="center">4.1</td>
</tr>
<tr>
<td align="left">Retinoblastoma</td>
<td align="center">3.0</td>
<td align="center">2.6</td>
<td align="center">7.1</td>
<td align="center">11.0</td>
<td align="center">4.8</td>
</tr>
<tr>
<td align="left">Nephroblastoma</td>
<td align="center">6.3</td>
<td align="center">5.6</td>
<td align="center">12.3</td>
<td align="center">14.0</td>
<td align="center">9.2</td>
</tr>
<tr>
<td align="left">Hepatic tumours</td>
<td align="center">1.3</td>
<td align="center">1.3</td>
<td align="center">2.1</td>
<td align="center">5.0</td>
<td align="center">1.1</td>
</tr>
<tr>
<td align="left">Malignant bone tumour</td>
<td align="center">4.7</td>
<td align="center">4.3</td>
<td align="center">4.5</td>
<td align="center">3.0</td>
<td align="center">3.2</td>
</tr>
<tr>
<td align="left">Soft tissue sarcomas</td>
<td align="center">7.0</td>
<td align="center">6.6</td>
<td align="center">9.5</td>
<td align="center">9.0</td>
<td align="center">6.7</td>
</tr>
<tr>
<td align="left">Germ cells tumour</td>
<td align="center">3.3</td>
<td align="center">3.6</td>
<td align="center">3.3</td>
<td align="center">2.0</td>
<td align="center">2.4</td>
</tr>
<tr>
<td align="left">Others tumours</td>
<td align="center">4.1</td>
<td align="center">4.6</td>
<td align="center">3.5</td>
<td align="center">5.0</td>
<td align="center">7.1</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>We found leukaemias to be the most frequent paediatric cancer, followed by lymphoma and Wilms tumour. This finding is similar to that reported in a previous study conducted in Khartoum.<sup><xref ref-type="bibr" rid="CIT0020">20</xref></sup> Similar findings have also been reported for countries in northern Africa, South Africa and Namibia.<sup><xref ref-type="bibr" rid="CIT0010">10</xref>,<xref ref-type="bibr" rid="CIT0028">28</xref>,<xref ref-type="bibr" rid="CIT0032">32</xref>,<xref ref-type="bibr" rid="CIT0033">33</xref></sup> This is in contrast to many LMICs, where leukaemias are much less frequent than lymphomas.<sup><xref ref-type="bibr" rid="CIT0008">8</xref>,<xref ref-type="bibr" rid="CIT0021">21</xref>,<xref ref-type="bibr" rid="CIT0022">22</xref>,<xref ref-type="bibr" rid="CIT0034">34</xref></sup> We found that most children with leukaemias were boys, which is also similar to that reported in other studies.<sup><xref ref-type="bibr" rid="CIT0023">23</xref>,<xref ref-type="bibr" rid="CIT0035">35</xref></sup> Most of the children in our analysis resided in rural regions of Sudan, where tertiary medical care is lacking. It is plausible that some children with leukaemia may have died before registration or diagnosis. Interestingly, during the first period (1999&#x2013;2005), lymphomas were the most frequently occurring cancers. In contrast, leukaemias were the most common cancer types in later periods (2006&#x2013;2010 and 2011&#x2013;2015). This could represent either a true increase in the incidence of leukaemias or an improvement in clinical and laboratory diagnoses or better registrations in the Cancer Registries.</p>
<p>In HICs, lymphomas are the third most common childhood cancer, following leukaemias and CNS tumours. We found that lymphomas were the second most frequent cancer type in children treated at the NCI. Similar findings have been reported for northern African countries, South Africa and India.<sup><xref ref-type="bibr" rid="CIT0024">24</xref>,<xref ref-type="bibr" rid="CIT0028">28</xref>,<xref ref-type="bibr" rid="CIT0036">36</xref></sup> This is in contrast to previous studies from other African countries that reported lymphomas as the most common tumours affecting the paediatric population.<sup><xref ref-type="bibr" rid="CIT0011">11</xref>,<xref ref-type="bibr" rid="CIT0022">22</xref>,<xref ref-type="bibr" rid="CIT0034">34</xref></sup> We found that the majority of children with lymphomas were older than 5 years, which is similar to the findings of a recent report from Yemen.<sup><xref ref-type="bibr" rid="CIT0029">29</xref></sup></p>
<p>In HICs, CNS tumours are the second most diagnosed cancers and represent 20&#x0025; to 27&#x0025; of all paediatric cancers.<sup><xref ref-type="bibr" rid="CIT0037">37</xref></sup> The incidence of CNS tumours in our study was lower than that reported in HICs. The incidence of CNS tumours is reduced in LMICs, which may reflect ethnic variation or limited neurosurgical resources or attenuated availability of advanced imaging equipment, such as CT and MRI scanners.<sup><xref ref-type="bibr" rid="CIT0008">8</xref>,<xref ref-type="bibr" rid="CIT0019">19</xref></sup> In the current study, the steep increase in the relative frequency of CNS tumours reported in the second and third periods (2006&#x2013;2010 and 2011&#x2013;2015) compared to the first period (1999&#x2013;2005) is likely because of the introduction of CT scan, MRI and neurosurgical services in central Sudan.</p>
<p>We found that nephroblastoma was the third most frequent cancer affecting children at the NCI. This finding is slightly higher than the findings observed by Jabeen et al., in which nephroblastoma accounted for 6.8&#x0025; of childhood cancers.<sup><xref ref-type="bibr" rid="CIT0038">38</xref></sup> According to the SACTR, nephroblastomas are the fourth most frequent childhood cancer in South Africa.<sup><xref ref-type="bibr" rid="CIT0010">10</xref></sup> The frequency and demographics of nephroblastoma in central Sudan are in accordance with those reported worldwide, in which nephroblastomas occur primarily in children less than 5 years and with equal frequency in boys and girls.</p>
<p>Retinoblastoma is the most common intraocular cancer in children. In most HICs, retinoblastoma represents 2.4&#x0025; to 4&#x0025; of all paediatric cancers.<sup><xref ref-type="bibr" rid="CIT0039">39</xref>,<xref ref-type="bibr" rid="CIT0040">40</xref></sup> This is similar to our findings but low when compared with the frequency of retinoblastoma reported in some LMICs.<sup><xref ref-type="bibr" rid="CIT0034">34</xref>,<xref ref-type="bibr" rid="CIT0041">41</xref></sup> The data from Africa suggest that, in many of the populations of sub-Saharan Africa, rates are rather higher than in HICs.<sup><xref ref-type="bibr" rid="CIT0011">11</xref></sup> We found that most retinoblastomas occurred in children younger than 5 years, which is similar to findings reported in other studies.<sup><xref ref-type="bibr" rid="CIT0011">11</xref>,<xref ref-type="bibr" rid="CIT0042">42</xref>,<xref ref-type="bibr" rid="CIT0043">43</xref></sup> Although retinoblastoma is highly curable if diagnosed early, most children with retinoblastoma who are referred to the NCI are at an advanced stage.<sup><xref ref-type="bibr" rid="CIT0044">44</xref></sup></p>
<p>Malignant bone tumours comprise approximately 5&#x0025; of childhood neoplasms.<sup><xref ref-type="bibr" rid="CIT0045">45</xref></sup> We observed that the rate of bone cancers was lower than expected. The causes of reduced incidence of childhood bone cancers at the NCI are unknown. The incidence of bone cancer is similar across the sexes and rises steeply with age.<sup><xref ref-type="bibr" rid="CIT0045">45</xref></sup> Concordantly, we found that more than two-thirds of the bone cancer cases reported at the NCI occurred in children aged 10 to 14 years, but most cases occurred in girls.</p>
<p>In most developed countries, neuroblastoma accounts for 6&#x0025; to 10&#x0025; of all childhood cancers. However, the frequency of neuroblastoma was reduced in children treated at the NCI during the study period. Low frequencies of neuroblastoma have also been reported in other sub-Saharan African countries, the percentage was between 3&#x0025; and 5&#x0025; of all childhood cancers seen (except Madagascar, where the frequency was 7.5&#x0025;).<sup><xref ref-type="bibr" rid="CIT0011">11</xref></sup> As expected, we found that most neuroblastoma cases occurred in children younger than 9 years, with the majority occurring in children younger than 5 years. We found that neuroblastoma predominantly affected female children. This is in contrast with other studies, which have identified the male sex as a risk factor for neuroblastoma.<sup><xref ref-type="bibr" rid="CIT0046">46</xref>,<xref ref-type="bibr" rid="CIT0047">47</xref></sup></p>
<p>Childhood carcinomas are rare. Consequently, they occurred infrequently in children with cancer who were treated at the NCI. Most of these cases occurred in children older than 9 years and in boys, which is similar to findings reported from Yemen.<sup><xref ref-type="bibr" rid="CIT0029">29</xref></sup> Nasopharyngeal carcinoma, which is very rare worldwide,<sup><xref ref-type="bibr" rid="CIT0048">48</xref></sup> was the most incident carcinoma in children at the NCI.</p>
<p>Primary neoplasms of the liver constitute 0.5&#x0025; to 2&#x0025; of cases in children younger than 15 years.<sup><xref ref-type="bibr" rid="CIT0049">49</xref></sup> At the NCI, we observed a similar frequency of liver cancers in children. Hepatitis B infection is considered as the most important factor associated with hepatocellular carcinoma in children.<sup><xref ref-type="bibr" rid="CIT0050">50</xref></sup> In Taiwan, Chiang et al. reported that the national hepatitis B vaccination programme that began in 1984 has been associated with over 70&#x0025; reduction in the liver cancer rates among children and adolescents.<sup><xref ref-type="bibr" rid="CIT0051">51</xref></sup> In our study, hepatitis B probably does not play a major role as the majority of liver tumours were in those under 4 years of age where they are almost certainly going to be hepatoblastomas.</p>
<p>Because our study was limited to a single institution, we cannot make conclusions on the general status of childhood cancers for all of Sudan. However, the NCI is the only cancer referral oncology institute in central Sudan; therefore, data from the NCI are the best indicator of the disease burden within this region. Nevertheless, this study provides insight into the characteristics of childhood cancers in a limited resource setting and lays the foundation for improvements in cancer care in Sudan. The findings of this study also have the potential to trigger further research into the area of childhood cancers in Sudan.</p>
</sec>
<sec id="s0009">
<title>Conclusion</title>
<p>This study provides baseline information about the epidemiology of childhood cancers in central Sudan by reviewing hospital records of patients who were treated at NCI. There was apparently rising incidence of childhood cancers associated with the growing influence of the specialised cancer centre in the region. Leukaemias and lymphomas constituted more than half of our study population. There was a low incidence of CNS tumours, which is a common finding in under-resourced settings. A population-based cancer registry is needed to determine the true incidence of childhood cancers in Sudan.</p>
</sec>
</body>
<back>
<ack>
<title>Acknowledgements</title>
<p>We thank Dr Nisha Badders from the Department of Scientific Editing at St. Jude Children&#x2019;s Research Hospital for editing the manuscript.</p>
<sec id="s20010" sec-type="COI-statement">
<title>Competing interests</title>
<p>The authors declare that they have no financial or personal relationships that may have inappropriately influenced them in writing this article.</p>
</sec>
<sec id="s20011">
<title>Authors contributions</title>
<p>M.M.A.E. was the project leader. M.M.A.E., A.A.M., N.O.Y., N.M.E., I.Q. and D.O.A. contributed to the design and implementation of the research, analysis of the results and writing of the manuscript.</p>
</sec>
</ack>
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<fn><p><bold>How to cite this article:</bold> Elhassan MMA, Mohamedani AA, Yousif NO, Elhaj NM, Qaddoumi I, Abuidres DO. Epidemiological review of childhood cancers in central Sudan. S. Afr. j. oncol. 2018;2(0), a37. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.4102/sajo.v2i0.37">https://doi.org/10.4102/sajo.v2i0.37</ext-link></p></fn>
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