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<article xmlns:xlink="http://www.w3.org/1999/xlink" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">jsocmed</journal-id><journal-title-group><journal-title>Journal of Society Medicine</journal-title></journal-title-group><issn pub-type="epub">2964-5565</issn><publisher><publisher-name>CoinReads Media Prima</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.71197/jsocmed.v5i5.303</article-id><article-categories><subj-group subj-group-type="heading"><subject>Original Research</subject></subj-group></article-categories><title-group><article-title>Clinicopathological Profile of Colorectal Cancer Patients at Dr. Zainoel Abidin General Hospital, Banda Aceh, Indonesia: A Single-Centre Retrospective Observational Study</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Subhan</surname><given-names>Nanda</given-names></name><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Razi </surname><given-names>Khalikul</given-names></name><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Meildi</surname><given-names>Maria</given-names></name><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Ilham </surname><given-names>Darul</given-names></name><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name><surname>Novhera </surname><given-names>T. Fenny</given-names></name><xref ref-type="aff" rid="aff5"/></contrib></contrib-group><aff id="aff1"><institution>Department of Surgery, Faculty of Medicine, Universitas Syiah Kuala / Zainoel Abidin General Hospital</institution></aff><aff id="aff2"><institution>Digestive Surgery Division, Department of Surgery, Faculty of Medicine Universitas Syiah Kuala- dr Zainoel Abidin General Hospital, Banda Aceh</institution>, <country>Indonesia</country></aff><aff id="aff3"><institution>Department of Surgery, Faculty of Medicine, Universitas Syiah Kuala / Zainoel Abidin General Hospital</institution></aff><aff id="aff4"><institution>Department of Surgery, Faculty of Medicine, Universitas Syiah Kuala / Zainoel Abidin General Hospital</institution></aff><aff id="aff5"><institution>Department of Surgery, Putri Bidadari Aceh Hospital</institution></aff><pub-date pub-type="epub"><year>2026</year><month>5</month><day>31</day></pub-date><volume>5</volume><issue>5</issue><history><date date-type="received"><day>11</day><month>5</month><year>2026</year></date><date date-type="accepted"><day>25</day><month>5</month><year>2026</year></date></history><permissions><copyright-year>2026</copyright-year><license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0"><license-p>This is an open access article distributed under the Creative Commons Attribution 4.0 International License.</license-p></license></permissions><abstract><p><bold>Introduction:</bold> Colorectal cancer (CRC) is a major global malignancy and a growing issue in Southeast Asia, with limited data from Indonesian hospitals outside Java. This study described demographic, anatomical, pathological, staging, and surgical characteristics of CRC patients at Dr. Zainoel Abidin General Hospital, Banda Aceh, in 2024.</p><p><bold>Methods:</bold> This retrospective study reviewed records of histopathologically confirmed CRC patients treated between January and December 2024. Incomplete records were excluded. Variables included age, sex, tumor location, AJCC stage, histological subtype, and surgical procedure. Continuous variables are mean ± standard deviation; categorical variables are frequencies and percentages with 95% confidence intervals. Statistical comparisons used chi-square goodness-of-fit, one-sample t-test, and proportion tests, with p &lt; 0.05 significant.</p><p><bold>Results:</bold> Fifty-seven patients were included. Mean age was 49.37 ± 12.4 years, significantly younger than the global reference of 60 years (p &lt; 0.001). Most were aged 46–65 years (57.9%), with males slightly predominating (54.4%). The rectum was the most common tumor site (56.1%), and stage III was most frequent (40.4%). Advanced-stage disease (stage III–IV) was observed in 52.6%. Adenocarcinoma accounted for 91.2%. Open laparotomy was the most common surgical approach (70.2%), followed by abdominoperineal resection, low anterior resection, and Hartmann procedure.</p><p><bold>Conclusion:</bold> CRC patients at RSUDZA in 2024 presented younger, with rectal predominance, frequent advanced-stage disease, and a dominance of open surgery, highlighting the need for earlier detection and surgical capacity in Aceh, Indonesia.</p></abstract></article-meta></front><body><sec id="introduction">
    <title>INTRODUCTION</title>
    <p>Colorectal cancer (CRC) is the third most frequently diagnosed
    malignancy and the second leading cause of cancer-related death
    worldwide, accounting for approximately 9.2% of cancer mortality and
    projected to increase substantially in low- and middle-income
    countries by 2035.¹,² CRC arises from the malignant transformation
    of glandular epithelium of the colon or rectum and is driven by an
    accumulation of genetic and epigenetic alterations modulated by age,
    dietary patterns, lifestyle, chronic inflammation, and inherited
    predisposition.³,⁴</p>
    <p>Although high-income settings have demonstrated marked declines
    in CRC mortality through population-based screening and improvements
    in multidisciplinary management, much of Southeast Asia continues to
    report rising incidence rates and a disproportionate burden of
    locally advanced disease at presentation.⁵–⁷ In Indonesia, CRC ranks
    among the four most common malignancies, with a notable proportion
    of patients diagnosed below the age of 50 years – the so-called
    early-onset phenotype.⁴,⁸</p>
    <p>Successful CRC management hinges on early detection, accurate
    staging and stage-appropriate surgical resection, increasingly
    delivered alongside neoadjuvant or adjuvant chemoradiotherapy.⁹–¹¹
    However, the case mix presenting to peripheral tertiary referral
    hospitals in Indonesia is shaped by local awareness, access to
    colonoscopy, and surgical capacity – factors that vary substantially
    across provinces.¹²,¹³ Aceh province in northern Sumatra is served
    by a single tertiary referral centre, Dr. Zainoel Abidin General
    Hospital (RSUDZA), yet contemporary descriptions of its CRC caseload
    are scarce. Robust local epidemiological data are a prerequisite for
    service planning, audit, and the design of region-specific screening
    interventions.</p>
    <p>This study therefore describes the demographic, anatomical,
    pathological and surgical profile of patients with CRC managed at
    RSUDZA in 2024, providing a quantitatively benchmarked baseline
    against published Indonesian and international data.</p>
  </sec>
  <sec id="methods">
    <title>METHODS</title>
    <sec id="study-design-and-setting">
      <title>Study design and setting</title>
      <p>This was a single-centre, retrospective, descriptive
      observational study conducted at the Department of Surgery,
      RSUDZA, Banda Aceh, Aceh, Indonesia. RSUDZA is the provincial
      tertiary referral centre serving a catchment population of
      approximately five million.</p>
    </sec>
    <sec id="population-and-sampling">
      <title>Population and sampling</title>
      <p>The study population comprised all patients with a
      histopathologically confirmed diagnosis of colorectal cancer who
      were managed by the digestive surgery service between 1 January
      and 31 December 2024. A total-sampling (consecutive) approach was
      used. Patients with incomplete medical records – defined as
      missing data on any of the predefined study variables – were
      excluded.</p>
    </sec>
    <sec id="variables-and-operational-definitions">
      <title>Variables and operational definitions</title>
      <p>Demographic variables comprised age (years; analysed
      continuously and categorised as 18–25, 26–45, 46–65, and &gt;65
      years) and sex. Clinico-pathological variables comprised: (i)
      anatomical location (caecum, ascending colon, transverse colon,
      descending colon, sigmoid colon, rectosigmoid, rectum); (ii) AJCC
      clinical stage at diagnosis (I, II, III, IV); (iii) histological
      type (adenocarcinoma versus other); and (iv) primary surgical
      procedure (exploratory laparotomy with tumour resection, low
      anterior resection [LAR], abdominoperineal resection [Miles
      procedure], Hartmann’s procedure).</p>
    </sec>
    <sec id="data-collection">
      <title>Data collection</title>
      <p>Data were extracted from the institutional medical record
      system using a standardised case-record form. Histopathology was
      reported by board-certified anatomical pathologists at RSUDZA, and
      staging was documented by the operating digestive surgeon based on
      intra-operative findings, imaging, and final histopathology, in
      accordance with AJCC 8th-edition criteria.</p>
    </sec>
    <sec id="statistical-analysis">
      <title>Statistical analysis</title>
      <p>Continuous variables are presented as mean ± SD; categorical
      variables as frequencies, percentages, and Wilson 95% CIs. To
      extend the original descriptive analysis, we performed the
      following inferential tests: (i) one-sample chi-square
      goodness-of-fit tests against a uniform distribution for each
      categorical variable; (ii) one-sample z-tests for proportion
      comparing observed proportions for the rectal site, adenocarcinoma
      histology, and male sex with externally reported Indonesian
      benchmarks (50.4%, 85%, and 50%, respectively); and (iii)
      one-sample t-tests comparing the cohort mean age with the global
      CRC reference mean (60 years) and with 50 years. A two-sided
      <italic>p</italic>-value &lt;0.05 was considered statistically
      significant. Analyses were performed in IBM SPSS Statistics
      version 22.0 (Armonk, NY, USA) and confirmed with open-source
      statistical routines.</p>
    </sec>
    <sec id="ethical-considerations">
      <title>Ethical considerations</title>
      <p>The study protocol was approved by the institutional review
      board of the Faculty of Medicine, Universitas Syiah Kuala /
      RSUDZA. As only de-identified secondary data were used, the
      requirement for individual informed consent was waived. The study
      was conducted in accordance with the Declaration of Helsinki.</p>
    </sec>
  </sec>
  <sec id="results">
    <title>RESULTS</title>
    <p>A total of 57 patients with histopathologically confirmed CRC met
    inclusion criteria during the study period.</p>
    <sec id="demographic-profile">
      <title>Demographic profile</title>
      <p>The mean age at diagnosis was 49.37 ± 12.4 years (range: 18–25
      to &gt;65 years). This mean was significantly lower than the
      international CRC mean of 60 years (t = −6.47, df = 56,
      <italic>p</italic> &lt; 0.001) but did not differ statistically
      from a reference of 50 years (t = −0.38, <italic>p</italic> =
      0.703), positioning the cohort precisely on the boundary of the
      early-onset definition. Patients aged 46–65 years comprised the
      largest stratum (33/57; 57.9%, 95% CI 45.0–69.8), followed by
      26–45 years (18/57; 31.6%), &gt;65 years (5/57; 8.8%) and 18–25
      years (1/57; 1.8%). The four-group age distribution departed
      markedly from a uniform expectation (χ² = 43.98, df = 3,
      <italic>p</italic> &lt; 0.001). Notably, 19 of 57 patients (33.3%,
      95% CI 22.4–46.3) were aged ≤45 years – an early-onset proportion
      higher than would be expected from a high-income setting and
      significantly different from the older subgroup distribution (χ² =
      6.33, df = 1, <italic>p</italic> = 0.012).</p>
      <p>Male patients accounted for 31 of 57 cases (54.4%, 95% CI
      41.6–66.6) and females for 26 (45.6%), giving a male-to-female
      ratio of 1.19:1. The sex distribution did not differ significantly
      from parity (χ² = 0.44, df = 1, <italic>p</italic> = 0.508), nor
      from the 50% null benchmark (z = 0.66, <italic>p</italic> = 0.508)
      (Table 1).</p>
      <p><bold>Table 1.</bold> Demographic distribution of patients with
      colorectal cancer at RSUDZA, 2024 (n = 57)</p>
      <table-wrap>
        <table>
          <colgroup>
            <col width="21%" />
            <col width="21%" />
            <col width="21%" />
            <col width="21%" />
          </colgroup>
          <thead>
            <tr>
              <th>Variable</th>
              <th>n</th>
              <th>%</th>
              <th>95% CI</th>
            </tr>
          </thead>
          <tbody>
            <tr>
              <td><bold>Age group (years)</bold></td>
              <td />
              <td />
              <td />
            </tr>
            <tr>
              <td>18–25</td>
              <td>1</td>
              <td>1.8</td>
              <td>0.3–9.4</td>
            </tr>
            <tr>
              <td>26–45</td>
              <td>18</td>
              <td>31.6</td>
              <td>20.7–44.9</td>
            </tr>
            <tr>
              <td>46–65</td>
              <td>33</td>
              <td>57.9</td>
              <td>45.0–69.8</td>
            </tr>
            <tr>
              <td>&gt;65</td>
              <td>5</td>
              <td>8.8</td>
              <td>3.8–18.9</td>
            </tr>
            <tr>
              <td>Mean ± SD: 49.37 ± 12.4 years</td>
              <td />
              <td />
              <td />
            </tr>
            <tr>
              <td><bold>Sex</bold></td>
              <td />
              <td />
              <td />
            </tr>
            <tr>
              <td>Male</td>
              <td>31</td>
              <td>54.4</td>
              <td>41.6–66.6</td>
            </tr>
            <tr>
              <td>Female</td>
              <td>26</td>
              <td>45.6</td>
              <td>33.4–58.4</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
    </sec>
    <sec id="anatomical-distribution">
      <title>Anatomical distribution</title>
      <p>The rectum was the most frequent primary site (32/57; 56.1%,
      95% CI 43.3–68.2), followed equally by the sigmoid colon and
      descending colon (6 each; 10.5%), ascending colon (5; 8.8%),
      transverse colon and caecum (3 each; 5.3%), and rectosigmoid
      junction (2; 3.4%) (Table 2). The seven-category distribution
      differed strongly from uniform expectation (χ² = 83.37, df = 6,
      <italic>p</italic> &lt; 0.001). When recategorised dichotomously,
      rectal cancers (with the rectosigmoid grouped as rectal: 34/57;
      59.6%) outnumbered colonic cancers (23/57; 40.4%), but the
      difference did not reach statistical significance (χ² = 2.12,
      <italic>p</italic> = 0.145). The observed rectal proportion was
      numerically higher than the 50.4% reported by Hamdi et al.⁴¹ but
      the difference was not statistically significant (z = 0.87,
      <italic>p</italic> = 0.386).</p>
      <p><bold>Table 2.</bold> Anatomical distribution of colorectal
      cancer (n = 57)</p>
      <table-wrap>
        <table>
          <colgroup>
            <col width="21%" />
            <col width="21%" />
            <col width="21%" />
            <col width="21%" />
          </colgroup>
          <thead>
            <tr>
              <th>Site</th>
              <th>n</th>
              <th>%</th>
              <th>95% CI</th>
            </tr>
          </thead>
          <tbody>
            <tr>
              <td>Rectum</td>
              <td>32</td>
              <td>56.1</td>
              <td>43.3–68.2</td>
            </tr>
            <tr>
              <td>Sigmoid colon</td>
              <td>6</td>
              <td>10.5</td>
              <td>4.9–21.1</td>
            </tr>
            <tr>
              <td>Descending colon</td>
              <td>6</td>
              <td>10.5</td>
              <td>4.9–21.1</td>
            </tr>
            <tr>
              <td>Ascending colon</td>
              <td>5</td>
              <td>8.8</td>
              <td>3.8–18.9</td>
            </tr>
            <tr>
              <td>Transverse colon</td>
              <td>3</td>
              <td>5.3</td>
              <td>1.8–14.4</td>
            </tr>
            <tr>
              <td>Caecum</td>
              <td>3</td>
              <td>5.3</td>
              <td>1.8–14.4</td>
            </tr>
            <tr>
              <td>Rectosigmoid</td>
              <td>2</td>
              <td>3.5</td>
              <td>1.0–11.9</td>
            </tr>
            <tr>
              <td>Goodness-of-fit: χ² = 83.37, df = 6,
              <italic>p</italic> &lt; 0.001</td>
              <td />
              <td />
              <td />
            </tr>
          </tbody>
        </table>
      </table-wrap>
    </sec>
    <sec id="stage-at-diagnosis">
      <title>Stage at diagnosis</title>
      <p>Stage III was the most frequent presentation (23/57; 40.4%, 95%
      CI 28.6–53.3), followed by stage II (17; 29.8%), stage I (10;
      17.5%) and stage IV (7; 12.3%) (Table 3). The four-stage
      distribution differed from uniform (χ² = 10.86, df = 3,
      <italic>p</italic> = 0.013). Aggregating into early (I–II) versus
      advanced (III–IV) disease yielded 27 (47.4%) versus 30 (52.6%)
      patients respectively – a near-even split (χ² = 0.16,
      <italic>p</italic> = 0.691) – indicating that more than half of
      all patients presented with locally advanced or metastatic disease
      at first surgical contact.</p>
      <p><bold>Table 3.</bold> Stage at diagnosis (n = 57)</p>
      <table-wrap>
        <table>
          <colgroup>
            <col width="21%" />
            <col width="21%" />
            <col width="21%" />
            <col width="21%" />
          </colgroup>
          <thead>
            <tr>
              <th>Stage</th>
              <th>n</th>
              <th>%</th>
              <th>95% CI</th>
            </tr>
          </thead>
          <tbody>
            <tr>
              <td>I</td>
              <td>10</td>
              <td>17.5</td>
              <td>9.8–29.4</td>
            </tr>
            <tr>
              <td>II</td>
              <td>17</td>
              <td>29.8</td>
              <td>19.1–43.2</td>
            </tr>
            <tr>
              <td>III</td>
              <td>23</td>
              <td>40.4</td>
              <td>28.6–53.3</td>
            </tr>
            <tr>
              <td>IV</td>
              <td>7</td>
              <td>12.3</td>
              <td>6.1–23.3</td>
            </tr>
            <tr>
              <td>Goodness-of-fit: χ² = 10.86, df = 3,
              <italic>p</italic> = 0.013; Advanced (III–IV) vs early
              (I–II): <italic>p</italic> = 0.691</td>
              <td />
              <td />
              <td />
            </tr>
          </tbody>
        </table>
      </table-wrap>
    </sec>
    <sec id="histopathology">
      <title>Histopathology</title>
      <p>Adenocarcinoma was the dominant histological type, identified
      in 52 of 57 specimens (91.2%, 95% CI 81.1–96.2). The remaining 5
      cases (8.8%) were classified as histopathologically confirmed CRC
      with documented metastatic disease at presentation, in line with
      the institutional reporting convention. The dominance of
      adenocarcinoma was highly significant relative to a 50% null (χ² =
      38.75, <italic>p</italic> &lt; 0.001), and was numerically higher
      than – though not significantly different from – the 85% benchmark
      commonly cited for CRC (z = 1.32, <italic>p</italic> = 0.188).</p>
    </sec>
    <sec id="surgical-management">
      <title>Surgical management</title>
      <p>Open exploratory laparotomy with tumour resection was performed
      in 40 patients (70.2%, 95% CI 57.3–80.5), the Miles
      abdominoperineal resection in 7 (12.3%), low anterior resection in
      6 (10.5%) and Hartmann’s procedure in 4 (7.0%) (Table 4). The
      procedural distribution was highly non-uniform (χ² = 62.37, df =
      3, <italic>p</italic> &lt; 0.001). Sphincter-preserving resections
      (LAR) accounted for 6 of 32 rectal cancers in this descriptive
      denominator (18.8%), while abdominoperineal resection accounted
      for 7 (21.9%); no laparoscopic colorectal resections were recorded
      during the study period.</p>
      <p><bold>Table 4.</bold> Distribution of surgical procedures (n =
      57)</p>
      <table-wrap>
        <table>
          <colgroup>
            <col width="21%" />
            <col width="21%" />
            <col width="21%" />
            <col width="21%" />
          </colgroup>
          <thead>
            <tr>
              <th>Procedure</th>
              <th>n</th>
              <th>%</th>
              <th>95% CI</th>
            </tr>
          </thead>
          <tbody>
            <tr>
              <td>Exploratory laparotomy with tumour resection</td>
              <td>40</td>
              <td>70.2</td>
              <td>57.3–80.5</td>
            </tr>
            <tr>
              <td>Miles abdominoperineal resection</td>
              <td>7</td>
              <td>12.3</td>
              <td>6.1–23.3</td>
            </tr>
            <tr>
              <td>Low anterior resection (LAR)</td>
              <td>6</td>
              <td>10.5</td>
              <td>4.9–21.1</td>
            </tr>
            <tr>
              <td>Hartmann’s procedure</td>
              <td>4</td>
              <td>7.0</td>
              <td>2.8–16.7</td>
            </tr>
            <tr>
              <td>Goodness-of-fit: χ² = 62.37, df = 3,
              <italic>p</italic> &lt; 0.001</td>
              <td />
              <td />
              <td />
            </tr>
          </tbody>
        </table>
      </table-wrap>
    </sec>
  </sec>
  <sec id="discussion">
    <title>DISCUSSION</title>
    <p>This single-centre audit of 57 consecutive CRC patients managed
    at RSUDZA in 2024 provides four observations of programmatic
    relevance. First, the mean age at presentation (49.37 ± 12.4 years)
    was significantly younger than the 60-year benchmark commonly
    reported in high-income registries (<italic>p</italic> &lt; 0.001),
    and one-third of the cohort was aged 45 years or less. This finding
    is concordant with reports from other Indonesian centres, including
    Widya et al.,³³ Asmaul Husnah et al.,³⁴ and Pratama et al.,³⁵ who
    similarly identified a downward shift in CRC age distribution. The
    early-onset phenotype is increasingly recognised as a global
    epidemiological trend driven by dietary westernisation, rising
    obesity prevalence, sedentary lifestyles, and possibly
    gut-microbiome alterations.²,⁴ Its statistical prominence in the
    present cohort underscores the limitations of using age 50 years as
    the sole threshold for CRC screening eligibility in the Indonesian
    context.</p>
    <p>Second, male predominance was modest and did not differ
    statistically from parity (54.4% vs 50%, <italic>p</italic> =
    0.508), consistent with Aritrina et al.³⁶ (58.6% male) and Yasri et
    al.³⁷ (59.4% male). The biological basis for the small but
    consistent excess in men is multifactorial and includes differences
    in visceral adiposity distribution, lifestyle exposures, and the
    putative protective effect of endogenous oestrogen on colonic
    epithelium.³⁶–³⁸</p>
    <p>Third, the rectum dominated the anatomical distribution (56.1%),
    a pattern that mirrors several Indonesian and Chinese reports³⁹–⁴²
    yet is the opposite of patterns described in many Western registries
    where colonic and right-sided tumours have become relatively more
    frequent. The non-uniformity of the seven-site distribution was
    unequivocal (<italic>p</italic> &lt; 0.001), although the
    dichotomous rectal-versus-colonic comparison did not reach
    significance, reflecting the moderate sample size. The rectal
    preponderance carries operational implications: rectal cancers
    demand multidisciplinary input, magnetic-resonance staging,
    neoadjuvant chemoradiotherapy in selected patients, and total
    mesorectal excision performed by appropriately trained surgeons.
    Late presentation with bulky low rectal tumours typically narrows
    the technical window for sphincter preservation.</p>
    <p>Fourth, the stage distribution was non-uniform
    (<italic>p</italic> = 0.013), with stage III as the modal category,
    and 52.6% of patients presenting with locally advanced (III) or
    metastatic (IV) disease. This profile is consistent with that of
    Widya et al.³³ (stage III: 41.0%), Indarti et al.⁴⁴ (stage III:
    38.2%) and Birch et al.⁴⁵ (stage III: 29.2%), and reflects a
    well-documented diagnostic delay in low- and middle-income settings
    driven by limited symptom literacy, reluctance to undergo per-rectal
    examination or colonoscopy, and constrained access to specialist
    diagnostic services.³³,⁴⁴,⁴⁵ Adenocarcinoma overwhelmingly dominated
    the histological mix (91.2%; <italic>p</italic> &lt; 0.001 vs equal
    split), in agreement with global figures of approximately
    85–90%.³⁹,⁴⁰,⁴⁶ The histogenetic basis lies in the abundance of
    mucin-secreting goblet cells in the colorectal mucosa and their
    susceptibility to malignant transformation under sustained
    carcinogen exposure.⁴¹,⁴⁷</p>
    <p>The procedural pattern – with 70.2% of cases managed by open
    laparotomy with tumour resection and no laparoscopic colorectal
    resections recorded – mirrors the experience of Salmiah et al.⁴⁸ at
    a comparable Sumatran centre and Breekveldt et al.⁴⁹ in the
    pre-screening Dutch period. The procedural distribution was highly
    non-uniform (<italic>p</italic> &lt; 0.001), reflecting the
    dominance of one pathway. The relative under-utilisation of LAR
    among rectal cancers in this descriptive denominator (18.8%) is
    consistent with the high proportion of low rectal tumours presenting
    at advanced stage, in whom abdominoperineal resection or palliative
    diversion remains the most defensible option. Expanding minimally
    invasive capability and embedding structured neoadjuvant pathways –
    with downstaging assessment and pelvic MRI – would be the most
    plausible single intervention to shift this procedural mix towards
    sphincter-preserving and laparoscopic options over the next planning
    cycle.⁴⁸–⁵⁰</p>
    <sec id="strengths-and-limitations">
      <title>Strengths and limitations</title>
      <p>Strengths include the use of consecutive total sampling over a
      defined calendar year, histopathological confirmation in all
      cases, and transparent quantitative benchmarking against external
      reference proportions. Limitations are intrinsic to the design:
      the single-centre, retrospective scope precludes inferences about
      provincial incidence; the modest sample size limits statistical
      power for between-variable association testing (e.g. sex × stage,
      location × procedure); and the absence of follow-up data prevents
      survival analysis. Cross-tabulated analyses of the relationship
      between, for example, age strata and stage, or location and
      procedure, would meaningfully extend the present descriptive
      baseline and are a recommended next step.</p>
    </sec>
  </sec>
  <sec id="conclusion">
    <title>CONCLUSION</title>
    <p>Among 57 patients with colorectal cancer managed at RSUDZA in
    2024, presentation was dominated by middle-aged adults (mean 49.4
    years), with rectal cancer (56.1%), stage III disease (40.4%), and
    adenocarcinoma histology (91.2%) as the modal categories, and open
    laparotomy as the principal surgical approach (70.2%). All
    categorical distributions departed significantly from a uniform null
    (<italic>p</italic> ≤ 0.013 throughout), and over half of the cohort
    presented with locally advanced or metastatic disease. These data
    justify (i) lowering the operational age threshold for opportunistic
    CRC screening in Aceh, (ii) strengthening symptom-based public
    health messaging targeting rectal red-flag symptoms, and (iii)
    investing in laparoscopic and sphincter-preserving capacity within
    the regional referral network. Multicentre, prospective registries
    with linked outcome data are required to consolidate these findings
    and to evaluate the impact of future service-level
    interventions.</p>
  </sec>
  <sec id="acknowledgements">
    <title>ACKNOWLEDGEMENTS</title>
    <p>The authors thank the staff of the Department of Surgery and the
    Medical Records Installation of Dr. Zainoel Abidin General Hospital
    for their assistance with data retrieval.</p>
  </sec>
  <sec id="conflict-of-interest">
    <title>CONFLICT OF INTEREST</title>
    <p>The authors declare no conflict of interest.</p>
  </sec>
  <sec id="funding">
    <title>FUNDING</title>
    <p>This research received no specific grant from any funding agency
    in the public, commercial, or not-for-profit sectors.</p>
  </sec>
  <sec id="ethical-approval">
    <title>ETHICAL APPROVAL</title>
    <p>Approved by the Research Ethics Committee, Faculty of Medicine,
    Universitas Syiah Kuala / RSUDZA. Individual informed consent was
    waived for the use of de-identified secondary data.</p>
  </sec>
  <sec id="author-contributions">
    <title>AUTHOR CONTRIBUTIONS</title>
    <p>SSW conceived the study, collected and analysed the data, and
    drafted the manuscript. KR supervised the work, contributed to
    interpretation, and revised the manuscript critically. Both authors
    approved the final version.</p>
  </sec>
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