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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">jct</journal-id>
      <journal-title-group>
        <journal-title>Journal of Cancer Therapy</journal-title>
      </journal-title-group>
      <issn pub-type="epub">2151-1942</issn>
      <issn pub-type="ppub">2151-1934</issn>
      <publisher>
        <publisher-name>Scientific Research Publishing</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.4236/jct.2026.178035</article-id>
      <article-id pub-id-type="publisher-id">jct-153161</article-id>
      <article-categories>
        <subj-group>
          <subject>Article</subject>
        </subj-group>
        <subj-group>
          <subject>Medicine</subject>
          <subject>Healthcare</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Volumetric Arc Therapy in the Treatment of Cervical Cancer: Experience of the Radiotherapy Department of Bogodogo University Hospital</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author" corresp="yes">
          <name name-style="western">
            <surname>Dao</surname>
            <given-names>Abou</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Sia</surname>
            <given-names>Nioka Pierre Xavier</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Panandtigri</surname>
            <given-names>Souleymane</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Coulibaly</surname>
            <given-names>Ismael</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Minoungou</surname>
            <given-names>Nicolas Apolos Abel</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Ouattara</surname>
            <given-names>Adama</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
      </contrib-group>
      <aff id="aff1"><label>1</label> Bogodogo University Hospital, University of Joseph Ki-Zerbo, Ouagadougou, Burkina Faso </aff>
      <aff id="aff2"><label>2</label> Radiotherapy Department of Tengandogo University Hospital, University of Joseph Ki-Zerbo, Ouagadougou, Burkina Faso </aff>
      <author-notes>
        <fn fn-type="conflict" id="fn-conflict">
          <p>The authors declare no conflicts of interest regarding the publication of this paper.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub">
        <day>10</day>
        <month>08</month>
        <year>2026</year>
      </pub-date>
      <pub-date pub-type="collection">
        <month>08</month>
        <year>2026</year>
      </pub-date>
      <volume>17</volume>
      <issue>08</issue>
      <fpage>397</fpage>
      <lpage>407</lpage>
      <history>
        <date date-type="received">
          <day>26</day>
          <month>06</month>
          <year>2026</year>
        </date>
        <date date-type="accepted">
          <day>10</day>
          <month>08</month>
          <year>2026</year>
        </date>
        <date date-type="published">
          <day>13</day>
          <month>08</month>
          <year>2026</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>© 2026 by the authors and Scientific Research Publishing Inc.</copyright-statement>
        <copyright-year>2026</copyright-year>
        <license license-type="open-access">
          <license-p> This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link> ). </license-p>
        </license>
      </permissions>
      <self-uri content-type="doi" xlink:href="https://doi.org/10.4236/jct.2026.178035">https://doi.org/10.4236/jct.2026.178035</self-uri>
      <abstract>
        <p><bold>Background:</bold>Cervical cancer remains a major public health problem, particularly in resource-limited countries where locally advanced forms are common. Volumetric modulated arc therapy (VMAT) represents a technological advancement that allows for more conformal irradiation of target volumes while limiting the dose to organs at risk. <bold>Objective:</bold>To describe the clinical, tumor, therapeutic, and outcome characteristics of patients irradiated for cervical cancer at the Bogodogo radiotherapy department. <bold>Methods:</bold>This was a retrospective, single-center cohort study with data collection conducted between March 2023 and October 2025. All patients irradiated for cervical cancer during the study period were included. Data were collected from medical records, department registers, and treatment planning documents, and then analyzed using IBM SPSS Statistics 2025. <bold>Results:</bold>Fifty-two patients were included. Hypertension was observed in 23.1% of cases, diabetes in 7.7%, and HIV in 5.8%. Invasive squamous cell carcinoma accounted for 96.2% of cases, 30.8% of patients had lymph node involvement, and 55.8% were classified as FIGO 2018 ≥ IIIA. All patients received chemoradiotherapy concurrent chemoradiotherapy; 46.2% had received induction chemotherapy and 11.5% had undergone surgery. At the last follow-up date, 88.5% of the patients were alive. <bold>Conclusion:</bold>This single‑institution series suggests that VMAT‑based concurrent chemoradiotherapy for cervical cancer is feasible in our setting and that most patients can complete treatment, with encouraging survival at early follow‑up. Further prospective work with detailed dosimetric, toxicity, and long-term outcome data is needed.</p>
      </abstract>
      <kwd-group kwd-group-type="author-generated" xml:lang="en">
        <kwd>Cancer</kwd>
        <kwd>Cervix</kwd>
        <kwd>VMAT</kwd>
        <kwd>CHU Bogodogo</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="sec1">
      <title>1. Introduction</title>
      <p>Cervical cancer remains a major global health problem and continues to disproportionately affect low- and middle-income countries, particularly in sub-Saharan Africa, where high incidence and mortality rates coexist with limited access to specialized cancer care [<xref ref-type="bibr" rid="B1">1</xref>][<xref ref-type="bibr" rid="B2">2</xref>]. This situation is linked to several factors, including diagnostic delays, insufficient screening, incomplete human papillomavirus vaccination coverage, and inequalities in access to surgery, external beam radiotherapy, and brachytherapy [<xref ref-type="bibr" rid="B1">1</xref>][<xref ref-type="bibr" rid="B2">2</xref>].</p>
      <p>Standard treatment for locally advanced cervical cancer relies on platinum-based concurrent chemoradiotherapy followed by brachytherapy, which remains an essential component of curative treatment [<xref ref-type="bibr" rid="B3">3</xref>]-[<xref ref-type="bibr" rid="B7">7</xref>]. Historical randomized trials have shown that combining cisplatin-based chemotherapy with radiotherapy significantly improves overall survival and progression-free survival compared to radiotherapy alone [<xref ref-type="bibr" rid="B3">3</xref>][<xref ref-type="bibr" rid="B8">8</xref>]. These data have subsequently been consolidated by meta-analyses confirming the benefit of concurrent chemoradiotherapy in the treatment of locally advanced cervical cancer [<xref ref-type="bibr" rid="B5">5</xref>]. At the same time, international guidelines emphasize that brachytherapy cannot be omitted or replaced by external beam radiotherapy alone, even when it relies on modern irradiation techniques [<xref ref-type="bibr" rid="B6">6</xref>][<xref ref-type="bibr" rid="B7">7</xref>].</p>
      <p>Technological advances in radiation oncology have led to the development of intensity-modulated radiotherapy and, subsequently, volumetric modulated arc therapy (VMAT), an advanced delivery technique that provides dynamic dose modulation during gantry rotation [<xref ref-type="bibr" rid="B9">9</xref>][<xref ref-type="bibr" rid="B10">10</xref>]. VMAT enables dynamic dose delivery through continuous rotation of the accelerator arm, modulation of the dose rate, and synchronized movement of the multileaf collimator blades [<xref ref-type="bibr" rid="B9">9</xref>][<xref ref-type="bibr" rid="B10">10</xref>]. This technique offers several potential advantages, including improved dose conformation to the target volume, better protection of organs at risk, reduced treatment time, and greater delivery efficiency compared to some conventional approaches or static IMRT plans [<xref ref-type="bibr" rid="B9">9</xref>]-[<xref ref-type="bibr" rid="B11">11</xref>].</p>
      <p>In cervical cancer, VMAT has shown promising dosimetric advantages, including improved target volume coverage and reduced irradiation of organs at risk such as the bladder, rectum, bowel, pelvic bone marrow, and femoral heads [<xref ref-type="bibr" rid="B11">11</xref>]-[<xref ref-type="bibr" rid="B14">14</xref>]. However, the magnitude of its clinical benefit may vary according to local expertise, treatment workflow, and integration with brachytherapy [<xref ref-type="bibr" rid="B9">9</xref>][<xref ref-type="bibr" rid="B11">11</xref>][<xref ref-type="bibr" rid="B14">14</xref>].</p>
      <p>In Africa, implementation of advanced radiotherapy techniques remains challenged by equipment shortages, limited brachytherapy capacity, and human resource constraints [<xref ref-type="bibr" rid="B2">2</xref>][<xref ref-type="bibr" rid="B15">15</xref>]. In Burkina Faso, published data on the use of VMAT for cervical cancer remain scarce. The present study therefore aimed to report the experience of the Radiotherapy Department of Bogodogo University Hospital in the management of cervical cancer with VMAT in a cohort of 52 patients.</p>
    </sec>
    <sec id="sec2">
      <title>2. Materials and Methods</title>
      <sec id="sec2dot1">
        <title>2.1. Study Design and Setting</title>
        <p>This was a retrospective, descriptive, single-center cohort study conducted at the Radiotherapy Department of Bogodogo University Hospital, Ouagadougou, Burkina Faso, from March 2023 to October 2025. The study was designed in accordance with the reporting principles for observational studies and focused on all patients treated with VMAT for cervical cancer during the study period.</p>
      </sec>
      <sec id="sec2dot2">
        <title>2.2. Study Period</title>
        <p>The study population consisted of all patients irradiated for cervical cancer during the study period. <bold>Inclusion criteria</bold> were: 1) histologically confirmed cervical cancer; 2) treatment with VMAT in our department between March 2023 and October 2025; and 3) availability of minimum required data on baseline characteristics, treatment, and follow‑up. <bold>Exclusion criteria</bold> were: 1) absence of histologic confirmation; or 2) medical records lacking key baseline or follow‑up information.</p>
        <p>Over the study period, 56 patients initiated VMAT for cervical cancer. Four were excluded (two with incomplete baseline records and two without post‑treatment follow‑up), leaving 52 patients for analysis.</p>
      </sec>
      <sec id="sec2dot3">
        <title>2.3. Data Collection and Staging Procedures</title>
        <p>Data were collected retrospectively using a standardized extraction form from medical charts, departmental records, and radiotherapy planning documents. Variables included medical history and comorbidities, clinicopathological features, treatment characteristics, and outcome status at the time of last news.</p>
        <p>FIGO 2018 staging was assigned using clinical examination (speculum and bimanual/rectovaginal examination) and cross‑sectional imaging. Pelvic MRI was the preferred modality; pelvic CT was used when MRI was not available. Abdominal and thoracic CT were performed when indicated. Nodal status (N0/N1) was determined from MRI and/or CT using radiologic criteria for pathologic lymph nodes (short‑axis diameter and morphology).</p>
      </sec>
      <sec id="sec2dot4">
        <title>2.4. Radiotherapy Treatment Parameters and Target Volumes</title>
        <p>External beam radiotherapy was delivered using VMAT on a linear accelerator. The prescribed dose to the pelvis was 45 - 50.4 Gy in 25 - 28 daily fractions of 1.8 - 2.0 Gy, 5 fractions per week. The clinical target volume (CTV) included the primary tumor (when visible), cervix, uterus, parametria, upper vagina, and pelvic lymph node regions (common, external, internal iliac and obturator chains; para‑aortic nodes in selected cases), in line with guideline‑based contouring recommendations. Planning target volumes were generated by adding 7 - 10 mm margins to the CTV, adjusted according to departmental practice [<xref ref-type="bibr" rid="B6">6</xref>][<xref ref-type="bibr" rid="B7">7</xref>][<xref ref-type="bibr" rid="B16">16</xref>]. Organs at risk included at least the bladder, rectum, small bowel or bowel bag, and femoral heads [<xref ref-type="bibr" rid="B7">7</xref>][<xref ref-type="bibr" rid="B16">16</xref>]. Concurrent chemotherapy consisted of weekly cisplatin 40 mg/m<sup>2</sup>, planned for five to six cycles depending on tolerance.</p>
        <p>Because intracavitary brachytherapy is not yet available in our institution, all patients received an external beam boost of 16 - 20 Gy to the cervix and involved lymph nodes. Nodal disease was treated with a simultaneous integrated boost in line with guidelines [<xref ref-type="bibr" rid="B6">6</xref>].</p>
      </sec>
      <sec id="sec2dot5">
        <title>2.5. Follow-Up</title>
        <p>Patients were assessed weekly during treatment, then at 1 month after treatment completion, and subsequently every 3 months. Outcome assessment in the present study was primarily based on vital status at last follow-up.</p>
      </sec>
      <sec id="sec2dot6">
        <title>2.6. Statistical Analysis</title>
        <p>Data were analyzed using IBM SPSS Statistics 2025. Categorical variables were summarized as frequencies and percentages. Mean survival time was reported when available in the source manuscript. Overall survival was estimated using the Kaplan-Meier method. Patients who were alive at last contact were censored on that date. Median follow‑up was calculated using the reverse Kaplan-Meier method.</p>
      </sec>
      <sec id="sec2dot7">
        <title>2.7. Primary and Secondary Endpoints</title>
        <p>The primary endpoint was overall survival (OS), defined as the time from histologic diagnosis to death from any cause or last contact. Patients alive at last contact were censored on that date. Secondary endpoints were descriptive and included baseline clinico‑pathological characteristics, treatment characteristics, and vital status at last follow‑up.</p>
      </sec>
      <sec id="sec2dot8">
        <title>2.8. Ethical Considerations</title>
        <p>The study was approved by the Ethics Committee of Bogodogo University Hospital and was conducted in accordance with data confidentiality and anonymity requirements.</p>
      </sec>
    </sec>
    <sec id="sec3">
      <title>3. Results</title>
      <p>A total of 52 patients irradiated for cervical cancer at the radiotherapy department of the Bogodogo University Hospital between March 2023 and October 2025 were included in the analysis. The mean age was 56.12 years, with a range of 30 to 83 years, and the median age was 55 years.</p>
      <sec id="sec3dot1">
        <title>3.1. Medical History and Comorbidities</title>
        <p>In terms of medical history, hypertension was reported in more than 20% of the cohort, while diabetes was present in a few patients. Asthma and HIV (Human Immunodeficiency Virus) were reported in some patients. Menopause at the time of diagnosis was noted in more than 70% of patients.</p>
        <p>Regarding lifestyle habits, no patient reported smoking or alcohol consumption. Surgical history was absent in most patients, while a hysterectomy was reported in approximately 10%. A family history of cancer was absent in 90% of cases; two patients reported breast cancer in a sister and one patient reported a family history of cervical cancer in her mother. <bold>Table 1</bold> summarizes the medical, surgical, and family history of patients treated with volumetric arc therapy for cervical cancer.</p>
        <p><bold>Table 1.</bold> Medical, surgical and family history of patients treated with volumetric arc therapy for cervical cancer (n = 52).</p>
        <table-wrap id="tbl1">
          <label>Table 1</label>
          <table>
            <tbody>
              <tr>
                <td>
                  <bold>Variable</bold>
                </td>
                <td>
                  <bold>Category</bold>
                </td>
                <td>
                  <bold>n</bold>
                </td>
                <td>
                  <bold>%</bold>
                </td>
              </tr>
              <tr>
                <td>High blood pressure</td>
                <td>Yes</td>
                <td>12</td>
                <td>23.1</td>
              </tr>
              <tr>
                <td>Diabetes</td>
                <td>Yes</td>
                <td>4</td>
                <td>7.7</td>
              </tr>
              <tr>
                <td>Asthma</td>
                <td>Yes</td>
                <td>1</td>
                <td>1.9</td>
              </tr>
              <tr>
                <td>Alcohol consumption</td>
                <td>No</td>
                <td>52</td>
                <td>100.0</td>
              </tr>
              <tr>
                <td>Smoking</td>
                <td>No</td>
                <td>52</td>
                <td>100.0</td>
              </tr>
              <tr>
                <td>Menopause at diagnosis</td>
                <td>Yes</td>
                <td>38</td>
                <td>73.1</td>
              </tr>
              <tr>
                <td>Surgical history</td>
                <td>Nothing</td>
                <td>47</td>
                <td>90.4</td>
              </tr>
              <tr>
                <td>Family history of cancer</td>
                <td>Nothing</td>
                <td>49</td>
                <td>94.2</td>
              </tr>
              <tr>
                <td>HIV</td>
                <td>Positive</td>
                <td>3</td>
                <td>5.8</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </sec>
      <sec id="sec3dot2">
        <title>3.2. Clinicopathological Characteristics</title>
        <p>Histopathological examination showed a clear predominance of invasive squamous cell carcinoma, while adenocarcinoma accounted for only 2 cases. The histological grade was moderately differentiated in 2/3 of the patients.</p>
        <p>Regarding disease extent, lymph node involvement was found in one-third of the patients. No patient had distant metastases at diagnosis, with the entire cohort classified as M0. Overall, the patients’ general condition was preserved, with a WHO performance status of 0 in almost half of the cases. According to the 2018 FIGO classification, the majority of patients had tumors at stage IIIA or higher. <bold>Table 2</bold> summarizes the clinico-tumor characteristics of patients treated with volumetric arc therapy for cervical cancer. <xref ref-type="fig" rid="fig1">Figure 1</xref> shows the distribution of patients according to their 2018 FIGO stage.</p>
      </sec>
      <sec id="sec3dot3">
        <title>3.3. Treatment Characteristics</title>
        <p>Induction chemotherapy had been administered to slightly less than half of the patients. Surgery for cervical cancer had been performed on a few patients.</p>
        <p>All patients received external beam radiotherapy and concurrent chemoradiotherapy. <bold>Tab</bold><bold>le 3</bold> presents the treatment characteristics and vital status at the last follow-up.</p>
        <p><bold>Table 2.</bold> Clinicopathological characteristics of patients treated with volumetric arc therapy for cervical cancer (n = 52 for each variable).</p>
        <table-wrap id="tbl2">
          <label>Table 2</label>
          <table>
            <tbody>
              <tr>
                <td>
                  <bold>Variable</bold>
                </td>
                <td>
                  <bold>Category</bold>
                </td>
                <td>
                  <bold>n</bold>
                </td>
                <td>
                  <bold>%</bold>
                </td>
              </tr>
              <tr>
                <td>Histological type</td>
                <td>Infiltrating squamous cell carcinoma</td>
                <td>50</td>
                <td>96.2</td>
              </tr>
              <tr>
                <td>Histological type</td>
                <td>Adenocarcinoma</td>
                <td>2</td>
                <td>3.8</td>
              </tr>
              <tr>
                <td>Histological grade</td>
                <td>Clearly differentiated</td>
                <td>11</td>
                <td>21.2</td>
              </tr>
              <tr>
                <td>Histological grade</td>
                <td>Moderately differentiated</td>
                <td>33</td>
                <td>63.5</td>
              </tr>
              <tr>
                <td>Histological grade</td>
                <td>Undifferentiated</td>
                <td>8</td>
                <td>15.4</td>
              </tr>
              <tr>
                <td>Lymph node stage</td>
                <td>N0</td>
                <td>36</td>
                <td>69.2</td>
              </tr>
              <tr>
                <td>Lymph node stage</td>
                <td>N1</td>
                <td>16</td>
                <td>30.8</td>
              </tr>
              <tr>
                <td>Metastatic stage</td>
                <td>M0</td>
                <td>52</td>
                <td>100.0</td>
              </tr>
              <tr>
                <td>PS WHO</td>
                <td>0</td>
                <td>25</td>
                <td>48.1</td>
              </tr>
              <tr>
                <td>PS WHO</td>
                <td>1</td>
                <td>25</td>
                <td>48.1</td>
              </tr>
              <tr>
                <td>PS WHO</td>
                <td>2</td>
                <td>2</td>
                <td>3.8</td>
              </tr>
              <tr>
                <td>FIGO Staging 2018</td>
                <td>≤IIb</td>
                <td>23</td>
                <td>44.2</td>
              </tr>
              <tr>
                <td>FIGO Staging 2018</td>
                <td>≥IIIA</td>
                <td>29</td>
                <td>55.8</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p>PS WHO: Performance status of World Health Organization; FIGO: International Federation of Gynaecologic and Obstetric.</p>
        <fig id="fig1">
          <label>Figure 1</label>
          <graphic xlink:href="https://html.scirp.org/file/8903720-rId15.jpeg?20260813030429" />
        </fig>
        <p><bold>Figure 1.</bold> Patient distribution according to FIGO 2018 tumor staging.</p>
        <p><bold>Table 3.</bold> Therapeutic characteristics and vital status at last follow-up (n = 52).</p>
        <table-wrap id="tbl3">
          <label>Table 3</label>
          <table>
            <tbody>
              <tr>
                <td>
                  <bold>Variable</bold>
                </td>
                <td>
                  <bold>Category</bold>
                </td>
                <td>
                  <bold>n</bold>
                </td>
                <td>
                  <bold>%</bold>
                </td>
              </tr>
              <tr>
                <td>Induction chemotherapy</td>
                <td>Yes</td>
                <td>24</td>
                <td>46.2</td>
              </tr>
              <tr>
                <td>Induction chemotherapy</td>
                <td>No</td>
                <td>28</td>
                <td>53.8</td>
              </tr>
              <tr>
                <td>Surgery</td>
                <td>Yes</td>
                <td>6</td>
                <td>11.5</td>
              </tr>
              <tr>
                <td>Surgery</td>
                <td>No</td>
                <td>46</td>
                <td>88.5</td>
              </tr>
              <tr>
                <td>Radiotherapy</td>
                <td>Yes</td>
                <td>52</td>
                <td>100.0</td>
              </tr>
              <tr>
                <td>Concurrent chemoradiation</td>
                <td>Yes</td>
                <td>52</td>
                <td>100.0</td>
              </tr>
              <tr>
                <td>State according to the latest news</td>
                <td>Alive</td>
                <td>46</td>
                <td>88.5</td>
              </tr>
              <tr>
                <td>State according to the latest news</td>
                <td>Deceased</td>
                <td>6</td>
                <td>11.5</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </sec>
      <sec id="sec3dot4">
        <title>3.4. Outcome at Last Follow-Up</title>
        <p>Overall survival, defined as the primary endpoint of this study, was 88.5% (46 patients were alive and 6 (11.5%) had died). The mean survival time was 1405 days (approximately 3.8 years; 95% CI 1289 - 1521 days) for the entire cohort. The median follow‑up was 793.50 days (240 to 1564 days). <xref ref-type="fig" rid="fig2">Figure 2</xref> shows the survival curve.</p>
        <fig id="fig2">
          <label>Figure 2</label>
          <graphic xlink:href="https://html.scirp.org/file/8903720-rId16.jpeg?20260813030429" />
        </fig>
        <p><bold>Figure 2.</bold>Overall survival curve for the study cohort.</p>
      </sec>
    </sec>
    <sec id="sec4">
      <title>4. Discussion</title>
      <p>This study presents the initial experience of the Bogodogo Radiotherapy Department with VMAT in the treatment of cervical cancer and shows that most patients were managed for locally advanced disease. More than half of the cohort had FIGO 2018 stage IIIA or higher disease, and nearly one-third had nodal involvement. This pattern is consistent with reports from sub-Saharan Africa, where limited screening coverage, delayed diagnosis, and barriers to referral contribute to the predominance of advanced-stage presentation [<xref ref-type="bibr" rid="B2">2</xref>][<xref ref-type="bibr" rid="B17">17</xref>][<xref ref-type="bibr" rid="B18">18</xref>].</p>
      <p>In sub-Saharan Africa, cervical cancer remains one of the leading reasons for gynecological radiotherapy, but its management is still heavily dependent on the availability of equipment, specialized personnel, and brachytherapy [<xref ref-type="bibr" rid="B2">2</xref>][<xref ref-type="bibr" rid="B19">19</xref>]. A recent systematic review showed that access to radiotherapy in sub-Saharan Africa remains limited by financial, geographic, logistical, and human constraints, with a direct impact on the quality and completeness of treatments [<xref ref-type="bibr" rid="B2">2</xref>]. In this context, the implementation of an advanced technique such as VMAT in a West African center represents a significant organizational and technological advancement [<xref ref-type="bibr" rid="B19">19</xref>].</p>
      <p>The marked predominance of invasive squamous cell carcinoma in the present series is also consistent with regional and international data [<xref ref-type="bibr" rid="B19">19</xref>][<xref ref-type="bibr" rid="B20">20</xref>]. In addition, most patients had preserved performance status, which likely contributed to the feasibility of concurrent chemoradiotherapy in this cohort. All patients received radiotherapy and concurrent chemoradiotherapy, suggesting relative consistency of treatment delivery at the institutional level.</p>
      <p>The treatment modalities observed in this study are consistent with contemporary standards. All patients received concurrent radiotherapy and chemoradiotherapy, while induction chemotherapy was used in only a portion of the cohort, and surgery remained a minority procedure [<xref ref-type="bibr" rid="B7">7</xref>][<xref ref-type="bibr" rid="B21">21</xref>]. This distribution is logical in a population dominated by locally advanced forms of the disease, for which chemoradiotherapy followed by brachytherapy is the standard treatment [<xref ref-type="bibr" rid="B6">6</xref>][<xref ref-type="bibr" rid="B7">7</xref>][<xref ref-type="bibr" rid="B21">21</xref>]. However, several African studies show that, beyond the recommendations, the actual implementation of this therapeutic standard remains inconsistent, particularly due to access delays, treatment interruptions, and the variable availability of brachytherapy [<xref ref-type="bibr" rid="B2">2</xref>][<xref ref-type="bibr" rid="B18">18</xref>][<xref ref-type="bibr" rid="B22">22</xref>].</p>
      <p>The growing use of VMAT in radiation oncology is mainly supported by dosimetric and logistical advantages, including improved dose conformity, sparing of pelvic organs at risk, and shorter treatment times in selected settings [<xref ref-type="bibr" rid="B9">9</xref>][<xref ref-type="bibr" rid="B10">10</xref>][<xref ref-type="bibr" rid="B12">12</xref>][<xref ref-type="bibr" rid="B13">13</xref>]. The literature also suggests that VMAT can help reduce certain treatment times and improve logistical feasibility in high-volume departments [<xref ref-type="bibr" rid="B9">9</xref>][<xref ref-type="bibr" rid="B14">14</xref>]. However, the current study does not yet provide detailed dosimetric data, toxicity outcomes, brachytherapy information, or full time-to-event analyses, which limits the ability to draw strong conclusions regarding long-term oncologic benefit [<xref ref-type="bibr" rid="B7">7</xref>][<xref ref-type="bibr" rid="B23">23</xref>].</p>
      <p>In this retrospective cohort, overall survival was prespecified as the primary endpoint, and our analysis remains essentially descriptive and hypothesisgenerating rather than designed to demonstrate definitive treatment benefit. The proportion of patients alive at last follow-up appears encouraging. Nevertheless, this result should be interpreted cautiously because the study did not provide a complete actuarial survival analysis, median follow-up duration, or detailed progression-related outcomes. For comparison, the experience of the National Radiotherapy Center in Accra, Ghana, involving 250 patients treated with external beam radiotherapy and brachytherapy, reported a 3-year overall survival rate of 86% with a median follow-up of 2.4 years [<xref ref-type="bibr" rid="B24">24</xref>]. This comparison suggests that the Bogodogo results are promising, but it also highlights the need for methodological refinement of the manuscript by adding data on survival, toxicities, brachytherapy, overall treatment time, and dosimetric parameters in order to more accurately assess the oncological and technical performance of this institutional experience [<xref ref-type="bibr" rid="B2">2</xref>][<xref ref-type="bibr" rid="B7">7</xref>][<xref ref-type="bibr" rid="B24">24</xref>].</p>
      <p>Limits of the study: First, the retrospective design and our inclusion of only 52 of the 56 patients who initiated VMAT may have introduced selection bias, because four patients with incomplete baseline data or missing followup were excluded from the analysis. This restriction to patients with more complete records and documented followup may overestimate treatment completion and survival, and our results should therefore be interpreted as exploratory institutional observations rather than populationlevel estimates.</p>
    </sec>
    <sec id="sec5">
      <title>5. Conclusion</title>
      <p>VMAT-based management of cervical cancer at the Bogodogo Radiotherapy Department mainly involved patients with locally advanced disease and relied primarily on concurrent chemoradiotherapy. The study supports the feasibility of implementing VMAT in a low‑resource African setting, but additional studies are required to better define toxicity, local control, and survival.</p>
    </sec>
  </body>
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