<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article
PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN"
       "https://jats.nlm.nih.gov/publishing/1.3/JATS-journalpublishing1-3.dtd">
<article xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" dtd-version="1.3" article-type="research-article" xml:lang="en">
 <front>
  <journal-meta>
   <journal-id journal-id-type="nlm-ta">Ulutas Med J</journal-id>
   <journal-title-group>
    <journal-title>The Ulutas Medical Journal</journal-title>
    <abbrev-journal-title>Ulutas Med J</abbrev-journal-title>
   </journal-title-group>
   <issn pub-type="ppub">2149-0430</issn>
   <issn pub-type="epub">2149-388X</issn>
   <publisher>
    <publisher-name>Hayriye Zehra Ulutaş</publisher-name>
   </publisher>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="doi">10.5455/umj.20230822070551</article-id>
   <article-id pub-id-type="publisher-id">166473</article-id>
   <article-categories>
    <subj-group subj-group-type="heading">
     <subject>Original Article</subject>
    </subj-group>
    <subj-group subj-group-type="subject">
     <subject>Gynaecology and Obstetrics</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title>The Impact of Body Mass Index on Clinical Characteristics and Treatment Outcomes in Endometrial Cancer Patients: A Comprehensive Analysis</article-title>
   </title-group>
   <contrib-group>
    <contrib contrib-type="author" corresp="yes">
     <contrib-id contrib-id-type="orcid" authenticated="false">https://orcid.org/0000-0002-3797-8227</contrib-id>
     <name name-style="western">
      <surname>Can</surname>
      <given-names>Behzat</given-names>
     </name>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Conceptualization" vocab-term-identifier="https://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Data curation" vocab-term-identifier="https://credit.niso.org/contributor-roles/data-curation/">Data curation</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Formal analysis" vocab-term-identifier="https://credit.niso.org/contributor-roles/formal-analysis/">Formal analysis</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Funding acquisition" vocab-term-identifier="https://credit.niso.org/contributor-roles/funding-acquisition/">Funding acquisition</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Investigation" vocab-term-identifier="https://credit.niso.org/contributor-roles/investigation/">Investigation</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Methodology" vocab-term-identifier="https://credit.niso.org/contributor-roles/methodology/">Methodology</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Project administration" vocab-term-identifier="https://credit.niso.org/contributor-roles/project-administration/">Project administration</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Resources" vocab-term-identifier="https://credit.niso.org/contributor-roles/resources/">Resources</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Software" vocab-term-identifier="https://credit.niso.org/contributor-roles/software/">Software</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Supervision" vocab-term-identifier="https://credit.niso.org/contributor-roles/supervision/">Supervision</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Validation" vocab-term-identifier="https://credit.niso.org/contributor-roles/validation/">Validation</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Visualization" vocab-term-identifier="https://credit.niso.org/contributor-roles/visualization/">Visualization</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Writing – original draft" vocab-term-identifier="https://credit.niso.org/contributor-roles/writing-original-draft/">Writing – original draft</role>
     <role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Writing – review &amp; editing" vocab-term-identifier="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing – review &amp; editing</role>
     <xref ref-type="aff" rid="aff1">1</xref>
    </contrib>
    <aff id="aff1">
     <label>1</label>
     <institution-wrap>
      <institution-id institution-id-type="ror">https://ror.org/03f2jcq85</institution-id>
      <institution>Diyarbakır Gazi Yaşargil Training and Research Hospital Department of Gyneacological Oncology, Turkey</institution>
     </institution-wrap>
    </aff>
   </contrib-group>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2023-09-13">
    <day>13</day>
    <month>09</month>
    <year>2023</year>
   </pub-date>
   <pub-date publication-format="print" date-type="collection">
    <year>2023</year>
   </pub-date>
   <volume>9</volume>
   <issue>3</issue>
   <fpage>145</fpage>
   <lpage>151</lpage>
   <history>
    <date date-type="received" iso-8601-date="2023-05-25">
     <day>25</day>
     <month>05</month>
     <year>2023</year>
    </date>
    <date date-type="rev-recd" iso-8601-date="2023-07-07">
     <day>07</day>
     <month>07</month>
     <year>2023</year>
    </date>
    <date date-type="accepted" iso-8601-date="2023-07-27">
     <day>27</day>
     <month>07</month>
     <year>2023</year>
    </date>
   </history>
   <permissions>
    <copyright-statement>© 2023 The Author(s)</copyright-statement>
    <copyright-year>2023</copyright-year>
    <license>
     <ali:license_ref>https://creativecommons.org/licenses/by-nc/4.0/</ali:license_ref>
     <license-p>This is an open access article distributed under the CC BY-NC 4.0 licence.</license-p>
    </license>
   </permissions>
   <self-uri xlink:href="https://www.ulutasmedicaljournal.com/?mno=166473"/>
   <self-uri content-type="pdf" xlink:href="https://www.ulutasmedicaljournal.com/pdf/166473.pdf"/>
   <abstract>
    <p>Introduction: The study investigates the influence of Body Mass Index (BMI) on demographic and clinical characteristics, the choice of treatment modalities, and their potential impact on treatment response and prognosis in endometrial cancer. Materials and Methods: This retrospective cohort study analyzed individuals diagnosed with endometrial cancer who underwent gynecological surgical interventions. BMI was calculated as weight (kg) divided by height (m) squared and categorized into four subgroups: overweight (BMI 25-29.9), obesity class 1 (BMI 30-34.9), obesity class 2 (BMI 35-39.9), and obesity class 3 (BMI ≥40). Demographic and clinical data were extracted from medical records. Results: Menopausal status differed across subgroups (p=0.013), with obesity class 3 showing a higher proportion of premenopausal women. Diabetes mellitus prevalence was higher in obesity class 3 (p=0.044). The usage of radiotherapy, brachytherapy, chemotherapy, and radiochemotherapy were similar across subgroups, as were relapse rates. The most commonly performed surgery was TAH+BSO+PPLND across all subgroups, with the highest percentage in the obesity class 3 (68.4%). The distribution of surgery types showed no difference across BMI subgroups (p=0.569). Conclusion: Our study highlights the potential influence of BMI on menopausal status and surgical treatment strategies in endometrial cancer patients. The findings emphasize the importance of considering BMI in managing endometrial cancer, given the rising global prevalence of obesity.</p>
   </abstract>
   <kwd-group kwd-group-type="author">
    <kwd>BMI</kwd>
    <kwd>endometrial cancer</kwd>
    <kwd>treatment outcomes</kwd>
    <kwd>surgical interventions</kwd>
   </kwd-group>
   <funding-group>
    <funding-statement>Funding information was not reported in the published version of this article.</funding-statement>
   </funding-group>
  </article-meta>
 </front>
 <body>
  <sec id="sec-1">
   <title>Introduction</title>
   <p id="b-1">The rising prevalence of obesity has spurred significant research interest in understanding its implications for various aspects of health (    <xref ref-type="bibr" rid="ref1">1</xref>
). The Body Mass Index (BMI) (    <xref ref-type="bibr" rid="ref2">2</xref>
), as an indicator of adiposity, has been widely employed to categorize individuals into different weight status groups (    <xref ref-type="bibr" rid="ref3">3</xref>
). These categories, ranging from overweight to severe obesity, provide insights into the potential health risks associated with differing degrees of adiposity (    <xref ref-type="bibr" rid="ref4">4</xref>
). Given strongly increasing global prevalence of obesity, it is crucial to comprehensively explore its impact on various demographic and clinical characteristics and its potential influence on the medical intervention and the treatment outcomes (    <xref ref-type="bibr" rid="ref4">4</xref>
,    <xref ref-type="bibr" rid="ref5">5</xref>
).</p>
   <p id="b-2">Endometrial cancer, a prevalent gynecologic malignancy, poses a significant public health concern worldwide (    <xref ref-type="bibr" rid="ref6">6</xref>
). It accounts for a substantial proportion of cancer-related morbidity and mortality among women (    <xref ref-type="bibr" rid="ref7">7</xref>
). While various risk factors have been identified for endometrial cancer, BMI, an established measure of adiposity, has emerged as a critical player in its aetiology (    <xref ref-type="bibr" rid="ref8">8</xref>
). Obesity has reached epidemic proportions, and its association with endometrial cancer risk has garnered considerable attention due to its potential to contribute to the increasing incidence of this malignancy (    <xref ref-type="bibr" rid="ref9">9</xref>
). Obesity, characterized by excess fatty tissue, disrupts hormonal balance, leading to chronic inflammation, insulin resistance, and altered sex hormone production (    <xref ref-type="bibr" rid="ref10">10</xref>
). These metabolic perturbations have been implicated in the pathogenesis of endometrial cancer, particularly in postmenopausal women (    <xref ref-type="bibr" rid="ref11">11</xref>
). As a result, investigating the relationship between BMI and endometrial cancer has become a focal point in clinical and epidemiological research (    <xref ref-type="bibr" rid="ref7">7</xref>
,    <xref ref-type="bibr" rid="ref11">11</xref>
,    <xref ref-type="bibr" rid="ref12">12</xref>
).</p>
   <p id="b-3">The complexity of endometrial cancer management extends beyond its initial diagnosis, encompassing surgical, medical, and radiotherapeutic interventions (    <xref ref-type="bibr" rid="ref13">13</xref>
). The effectiveness of these treatments can be influenced by BMI (    <xref ref-type="bibr" rid="ref14">14</xref>
). An in-depth analysis of how BMI affects the choice of treatment modalities and its impact on treatment response and prognosis is essential for tailoring therapeutic approaches to the unique needs of individual patients (    <xref ref-type="bibr" rid="ref15">15</xref>
). By investigating the influence of BMI, we aim to contribute valuable insights that can inform evidence-based clinical decision-making. This study aims to evaluate the relationship between BMI and endometrial cancer treatment outcomes.</p>
  </sec>
  <sec id="sec-2">
   <title>Materials and Methods</title>
  </sec>
  <sec id="sec-3">
   <title>Study design</title>
   <p id="b-4">This retrospective cohort study investigates the intricate interplay between BMI subgroups and a range of demographic and clinical variables in a cohort of individuals diagnosed with endometrial cancer who underwent gynaecological surgical interventions. We analysed clinical characteristics of individuals across different BMI subgroups.</p>
  </sec>
  <sec id="sec-4">
   <title>Ethical Statement</title>
   <p id="b-5">This retrospective analysis was conducted following the Declaration of Helsinki and approved by the Hospital's Institutional Review Board (Date: 03/11/2022 – Approval: 10-01). All patient data were anonymized to ensure privacy and confidentiality.</p>
   <sec id="sec-5">
    <title>Data Collection</title>
    <p id="b-6">Demographic and clinical data were extracted from medical records, including age, height, weight, parity, mode of delivery, menopausal status, marital status, employment status, monthly income, smoking history, diabetes mellitus, ECOG (Eastern Cooperative Oncology Group) score, comorbidity, and education level. BMI was calculated as weight (kg) divided by height (m) squared and categorized into four subgroups: overweight (BMI 25-29.9), obesity class 1 (BMI 30-34.9), obesity class 2 (BMI 35- 39.9), and obesity class 3 (BMI ≥40). The types of operations were recorded: total abdominal hysterectomy+bilateralSalpingooophorectomy (TAH+BSO), total abdominal hysterectomy + bilateral salpingo-oophorectomy+pelvic lymph dissection (TAH+BSO+PLND), total abdominal hysterectomy+bilateral Salpingooophorectomy para-aortic lymph node dissection (TAH+BSO+ PPLND), total laparoscopic hysterectomy+ bilateral salpingooophorectomy (TLH+BSO), total laparoscopic hysterectomy + bilateral salpingo-oophorectomy with pelvic lymph node dissection (TLH+BSO+PLND), and total laparoscopic hysterectomy + bilateral salpingo-oophorectomy + para-aortic lymph node dissection (TLH+BSO+PPLND).</p>
   </sec>
   <sec id="sec-6">
    <title>Statistical Analysis</title>
    <p id="b-7">Categorical variables were presented as numbers and percentages, while continuous variables were summarized using means±SD. As appropriate, comparisons between BMI subgroups were performed using the chi-square test or Fisher's exact test for categorical variables and one-way analysis of variance (ANOVA) or the Kruskal-Wallis test for continuous variables. All tests were two-sided; p-value&lt;0.05 was considered significant. All the statistical analyses were conducted using [SPSS, IBM, USA].</p>
   </sec>
  </sec>
  <sec id="sec-7">
   <title>Results</title>
   <p id="b-8">As seen in Table-1, there are no differences among the subgroups concerning age and height (p=0.718 and p=0.061, respectively). Examining reproductive history, parity did not differ across the subgroups (p=0.879). Additionally, the mode of delivery did not significantly differ among the subgroups (p=0.268). In terms of menopausal status, our analysis reveals a difference across the subgroups (p=0.013), with a higher percentage of premenopausal women in the obesity class 3 subgroup compared to other subgroups. We observed no marital and employment status differences among the subgroups (p=0.738 and p=0.312, respectively). There were no differences in monthly income and smoking habits across the subgroups (p=0.559 and p=0.455, respectively). We noted that diabetes mellitus was more prevalent in the obesity class 3 (p=0.044).However, there were no differences in the prevalence of comorbidity and ECOG (p=0.236). Education levels among the subgroups did not differ either (p=0.079).</p>
   <p id="b-9">As seen in Table-2, the usage of radiotherapy was higher in the obesity class 3 compared to others, but the difference was not significant (p=0.155). The proportion of patients receiving brachytherapy was slightly lower in the obesity class 2, with no difference among subgroups (p=0.194). The application of chemotherapy and radiochemotherapy were similar among the subgroups, with no distinctions (p=0.982 and p=0.481, respectively). Relapse rates were similar across the BMI subgroups, with only the overweight and obesity class 2 having any relapses (p=0.322). Regarding grading, the obesity class 2 had a higher proportion of grade 3 patients. However, the differences were not significant (p=0.093).</p>
   <p id="b-10">The most commonly performed surgery across all subgroups was TAH+BSO+PPLND, with the highest percentage observed in the obesity class 3 subgroup (68.4%). This surgery was chosen in more than half of the individuals in each subgroup, ranging from 55% in obesity class 1 to 68.4% in obesity class 3. Conversely, TAH+BSO was the least performed surgery among the subgroups, with the lowest percentage in the class 3 and overweight subgroups, at 10.5%. Similarly, TLH+BSO+ PLND and TLH+BSO+PPLND were infrequently performed across all subgroups. Interestingly, no individual in the obesity class 2 subgroup underwent TLH+BSO+PLND and no individuals in the overweight and class 3 experienced TLH+BSO+PLND. We found no difference when comparing the distribution of surgery types across the BMI subgroups (p=0.569).</p>
  </sec>
  <sec id="sec-8">
   <title>Discussion</title>
   <p id="b-11">Our retrospective comprehensive analysis of the relationship between BMI subgroups and endometrial cancer treatment outcomes offers several key insights into the intricate interplay between BMI, characteristics, and treatment strategies for endometrial cancer patients. This study underscores the importance of considering BMI as a critical factor in managing endometrial cancer, given its potential influence on characteristics and treatment outcomes. Novel studies have explored the connection between obesity and outcomes in treatment of endometrial cancer. In research by Kokts- Porietis et al. (    <xref ref-type="bibr" rid="ref16">16</xref>
), obese endometrial cancer survivors faced higher recurrence risks. Ward et al. (    <xref ref-type="bibr" rid="ref17">17</xref>
) found that cardiovascular diseases were the most common cause of death among women diagnosed with endometrial cancer. They observed a poorer preoperative health status with a BMI&gt;30, indicative of existing chronic health issues. Onstad et al. (    <xref ref-type="bibr" rid="ref18">18</xref>
) argued that performing surgery on obese patients with endometrial cancer could be more complex due to the technical aspects of the procedure. However, the choice of surgical procedures was not affected by obesity. This finding mirrors those of Gabala et al. (    <xref ref-type="bibr" rid="ref19">19</xref>
) as well as Erkanli et al. (    <xref ref-type="bibr" rid="ref20">20</xref>
). This is in contrast to findings by Bouwman et al. (    <xref ref-type="bibr" rid="ref21">21</xref>
), who reported that obese patients undergoing laparotomy were at higher risk for postoperative complications. Factors such as patient characteristics, the surgeon's experience, and the equipment used might account for the discrepancies (    <xref ref-type="bibr" rid="ref15">15</xref>
). Interestingly, our study found no differences among the BMI subgroups regarding age, height, parity, mode of delivery, marital and employment status, smoking habits, comorbidity, and ECOG.</p>
   <table-wrap id="tbl-1" position="float">
    <label>Table 1</label>
    <caption>
     <title>Demographic and clinical characteristics of individuals across different BMI subgroups</title>
    </caption>
    <graphic xlink:href="tbl-1.png">
     <alt-text>Table 1: Demographic and clinical characteristics of individuals across different BMI subgroups</alt-text>
    </graphic>
   </table-wrap>
   <table-wrap id="tbl-2" position="float">
    <label>Table 2</label>
    <caption>
     <title>Distribution of Treatment Methods and Outcomes by Obesity Class in Patients</title>
    </caption>
    <graphic xlink:href="tbl-2.png">
     <alt-text>Table 2: Distribution of Treatment Methods and Outcomes by Obesity Class in Patients</alt-text>
    </graphic>
   </table-wrap>
   <p id="b-12">Notably, diabetes mellitus was more prevalent in the obesity class 3, suggesting that higher BMI may be associated with an increased risk of comorbid conditions such as diabetes. This finding aligns with previous research that has established a link between obesity and type-2 diabetes mellitus. It highlights the importance of carefully managing diabetes in endometrial cancer, as it can affect treatment outcomes. Regarding menopausal status, our analysis revealed a higher proportion of premenopausal women in the obesity class 3 compared to other subgroups. Obesity can influence hormonal balance and contribute to alterations in sex hormone production, which may, in turn, affect menopausal status and reproductive history in endometrial cancer patients (    <xref ref-type="bibr" rid="ref4">4</xref>
,    <xref ref-type="bibr" rid="ref20">20</xref>
,    <xref ref-type="bibr" rid="ref22">22</xref>
). Obesity-associated chronic inflammation and insulin resistance have been implicated in endometrial carcinogenesis, particularly in postmenopausal women (    <xref ref-type="bibr" rid="ref11">11</xref>
,    <xref ref-type="bibr" rid="ref19">19</xref>
). Thus, our finding underscores the potential influence of BMI on endometrial cancer risk and the importance of considering menopausal status in endometrial cancer management.</p>
   <p id="b-13">Regarding treatment modalities, we observed no differences in the use of radiotherapy, brachytherapy, chemotherapy, radio-chemo therapy, and relapse rates across the BMI subgroups. However, distribution of surgical procedures revealed that the most commonly performed surgery across all subgroups was TAH+BSO+PPLND, with the highest percent observed in the obesity class 3 subgroup. Notably, TAH+BSO was the least performed surgery among the subgroups, with the lowest rate in the obesity class 3 and overweight subgroups. This may suggest that individuals with higher BMI may be more likely to undergo more extensive surgical procedures, possibly due to the increased complexity of their cases. However, we found no differences in the surgery types across the BMI subgroups.</p>
   <p id="b-14">There are some limitations. The retrospective nature of our analysis may introduce selection bias, and the data may not be entirely representative of the broader population. Additionally, our study's sample size may limit our findings' generalizability. More extensive prospective studies are needed to validate our findings and further explore the impact of BMI on endometrial cancer treatment outcomes.</p>
  </sec>
  <sec id="sec-9">
   <title>Conclusion</title>
   <p id="b-15">Our analysis offers valuable insights into the relationship between BMI and endometrial cancer treatment outcomes. While we observed no differences among the BMI subgroups regarding most demographic and clinical characteristics, our study highlights potential influence of BMI on menopausal status and surgical treatment strategies in endometrial cancer. Considering the increasing global prevalence of obesity, our findings underscore the importance of considering BMI as a critical factor in managing endometrial cancer. Further research is needed to elucidate the complex interplay between BMI, demographic and clinical characteristics, and treatment outcomes in endometrial cancer patients.</p>
  </sec>
 </body>
 <back>
  <ref-list>
   <title>References</title>
   <ref id="ref1">
    <label>1</label>
    <mixed-citation publication-type="journal">Fink J, Seifert G, Blüher M, Fichtner-Feigl S, Marjanovic G. Obesity Surgery. Dtsch Arztebl Int. 2022;119(5):70-80.</mixed-citation>
   </ref>
   <ref id="ref2">
    <label>2</label>
    <mixed-citation publication-type="journal">Khanna D, Peltzer C, Kahar P, Parmar MS. Body Mass Index (BMI): A Screening Tool Analysis. Cureus. 2022;14(2):e22119.</mixed-citation>
   </ref>
   <ref id="ref3">
    <label>3</label>
    <mixed-citation publication-type="journal">Petersen Harrington S, Balmaceda J, Spoozak L, Jewell A, Fitzgerald-Wolff S. Higher baseline BMI and lower estimated median income associated with increasing BMI after endometrial cancer diagnosis. Gynecol Oncol Rep. 2022;44: 101123.</mixed-citation>
   </ref>
   <ref id="ref4">
    <label>4</label>
    <mixed-citation publication-type="journal">Eakin CM, Liao CI, Salani R, Cohen JG, Kapp DS, Chan JK. The association of obesity with type I uterine cancer-is this an oversimplification? Am J Obstet Gynecol. 2022;227(3): 538-9.</mixed-citation>
   </ref>
   <ref id="ref5">
    <label>5</label>
    <mixed-citation publication-type="journal">Bo LL, Wang YQ, Liu YY, Li XD, Zhou R, Wang JL. [Analyze of obesity indicators and effect of fertility preservation treatment in patients with endometrial atypical hyperplasia and early endometrial cancer]. Zhonghua Fu Chan Ke Za Zhi. 2022;57(10):767-74.</mixed-citation>
   </ref>
   <ref id="ref6">
    <label>6</label>
    <mixed-citation publication-type="journal">Anic K, Flohr F, Schmidt MW, Krajnak S, Schwab R, Schmidt M, et al. Frailty assessment tools predict perioperative outcome in elderly patients with endometrial cancer better than age or BMI alone: a retrospective observational cohort study. J Cancer Res Clin Oncol. 2023;149(4):1551-60.</mixed-citation>
   </ref>
   <ref id="ref7">
    <label>7</label>
    <mixed-citation publication-type="journal">Petersdorf K, Groettrup-Wolfers E, Overton PM, Seitz C, Schulze-Rath R. Endometrial hyperplasia in premenopausal women: A systematic review of incidence, prevalence, and risk factors. Eur J Obstet Gynecol Reprod Biol. 2022; 271:158-71.</mixed-citation>
   </ref>
   <ref id="ref8">
    <label>8</label>
    <mixed-citation publication-type="journal">Driver JA, Viswanathan AN. Frailty measure is more predictive of outcomes after curative therapy for endometrial cancer than traditional risk factors in women 60 and older. Gynecol Oncol. 2017;145(3):526-30.</mixed-citation>
   </ref>
   <ref id="ref9">
    <label>9</label>
    <mixed-citation publication-type="journal">Belladelli F, Montorsi F, Martini A. Metabolic syndrome, obesity and cancer risk. Curr Opin Urol. 2022;32(6):594-7.</mixed-citation>
   </ref>
   <ref id="ref10">
    <label>10</label>
    <mixed-citation publication-type="journal">Wiley RL, Urbauer DL, Nugent E, Gallegos J, Ramondetta L. Endometrial cancer patients understanding and interest in weight loss surgery. Gynecol Oncol. 2023;175:88-92.</mixed-citation>
   </ref>
   <ref id="ref11">
    <label>11</label>
    <mixed-citation publication-type="journal">King L, Gajarawala S, McCrary MD. Endometrial cancer and obesity: Addressing the awkward silence. Jaapa. 2023;36(1):28-31. 151 77 Body Mass Index and Endometrial Cancer Behzat Can</mixed-citation>
   </ref>
   <ref id="ref12">
    <label>12</label>
    <mixed-citation publication-type="journal">Markowska A, Chudecka-Głaz A, Pityński K, Baranowski W, Markowska J, Sawicki W. Endometrial Cancer Management in Young Women. Cancers (Basel). 2022;14(8).</mixed-citation>
   </ref>
   <ref id="ref13">
    <label>13</label>
    <mixed-citation publication-type="journal">Agnew H, Kitson S, Crosbie EJ. Interventions for weight reduction in obesity to improve survival in women with endometrial cancer. Cochrane Database Syst Rev. 2023;3(3):Cd012513.</mixed-citation>
   </ref>
   <ref id="ref14">
    <label>14</label>
    <mixed-citation publication-type="journal">Petersen Harrington S, Balmaceda J, Spoozak L, Jewell A, Fitzgerald-Wolff S. Higher baseline BMI and lower estimated median income is associated with increasing BMI after endometrial cancer diagnosis. Gynecol Oncol Rep. 2022;44(Suppl 1):101109.</mixed-citation>
   </ref>
   <ref id="ref15">
    <label>15</label>
    <mixed-citation publication-type="journal">van der Woude H, Hally KE, Currie MJ, Gasser O, Henry CE. Importance of the endometrial immune environment in endometrial cancer and associated therapies. Front Oncol. 2022;12:975201.</mixed-citation>
   </ref>
   <ref id="ref16">
    <label>16</label>
    <mixed-citation publication-type="journal">Kokts-Porietis RL, Elmrayed S, Brenner DR, Friedenreich CM. Obesity and mortality among endometrial cancer survivors: A systematic review and meta-analysis. Obes Rev. 2021;22(12):e13337.</mixed-citation>
   </ref>
   <ref id="ref17">
    <label>17</label>
    <mixed-citation publication-type="journal">Ward KK, Shah NR, Saenz CC, McHale MT, Alvarez EA, Plaxe SC. Cardiovascular disease is the leading cause of death among endometrial cancer patients. Gynecol Oncol. 2012;126(2):176-9.</mixed-citation>
   </ref>
   <ref id="ref18">
    <label>18</label>
    <mixed-citation publication-type="journal">Onstad MA, Schmandt RE, Lu KH. Addressing the Role of Obesity in Endometrial Cancer Risk, Prevention, and Treatment. J Clin Oncol. 2016;34(35):4225-30.</mixed-citation>
   </ref>
   <ref id="ref19">
    <label>19</label>
    <mixed-citation publication-type="journal">Gaballa K, Abdelkhalek M, Refky B, Gadelhak B, Aboelnaga EM, El-Beshbishi W. The Impact of Obesity on Surgical Complications and Disease Recurrence in Endometrial Cancer: A Retrospective Study of 267 Patients. Research in Oncology. 2020;16(1):11-4.</mixed-citation>
   </ref>
   <ref id="ref20">
    <label>20</label>
    <mixed-citation publication-type="journal">Erkanli S, Kayaselçuk F, Bagis T, Kuşçu E. Impact of morbid obesity in surgical management of endometrial cancer: surgical morbidity, clinical and pathological aspects. Eur J Gynaecol Oncol. 2006;27(4):401-4.</mixed-citation>
   </ref>
   <ref id="ref21">
    <label>21</label>
    <mixed-citation publication-type="journal">Bouwman F, Smits A, Lopes A, Das N, Pollard A, Massuger L, et al. The impact of BMI on surgical complications and outcomes in endometrial cancer surgery--an institutional study and systematic review of the literature. Gynecol Oncol. 2015;139(2):369-76.</mixed-citation>
   </ref>
   <ref id="ref22">
    <label>22</label>
    <mixed-citation publication-type="journal">Chen J, Ke K, Liu Z, Yang L, Wang L, Zhou J, et al. Body Mass Index and Cancer Risk: An Umbrella Review of Meta-Analyses of Observational Studies. Nutr Cancer. 2023;75(4):1051-64.</mixed-citation>
   </ref>
  </ref-list>
 </back>
</article>
