<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJU</journal-id><journal-title-group><journal-title>Open Journal of Urology</journal-title></journal-title-group><issn pub-type="epub">2160-5440</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oju.2024.142008</article-id><article-id pub-id-type="publisher-id">OJU-131239</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Prostate Cancer in the Thies Region, Senegal: Epidemiological, Diagnostic and Therapeutic Aspects
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Saint</surname><given-names>Charles Nabab Kouka</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Linda</surname><given-names>Bentefouet</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mohamed</surname><given-names>Jalloh</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ngor</surname><given-names>Mack Thiam</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Modou</surname><given-names>Faye</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Modou</surname><given-names>Diop</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mohamed</surname><given-names>Cisse</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Amy</surname><given-names>Diame</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yoro</surname><given-names>Diallo</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Cheickna</surname><given-names>Sylla</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Urology, Faculty of Health Sciences, University Iba Der Thiam of Thies, Thies, Senegal</addr-line></aff><aff id="aff2"><addr-line>Department of Anatomy Pathology, Faculty of Health Sciences, University Iba Der Thiam of Thies, Thies, Senegal</addr-line></aff><aff id="aff3"><addr-line>Department of Urology, University Cheikh Anta Diop De Dakar, Dakar, Senegal</addr-line></aff><pub-date pub-type="epub"><day>04</day><month>02</month><year>2024</year></pub-date><volume>14</volume><issue>02</issue><fpage>71</fpage><lpage>82</lpage><history><date date-type="received"><day>14,</day>	<month>November</month>	<year>2023</year></date><date date-type="rev-recd"><day>18,</day>	<month>February</month>	<year>2024</year>	</date><date date-type="accepted"><day>21,</day>	<month>February</month>	<year>2024</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Introduction: Prostate cancer is the leading urological cancer. It is the most common cancer in men over 50. 
  Objective: To determine the epidemiological, diagnostic and therapeutic characteristics of prostate cancer in hospitals in the Thi&#232;s region. 
  Patients and Methods: We conducted a descriptive study from January 1
  <sup>st</sup>, 2015 to December 31
  <sup>st</sup>, 2020. We included all cases of primary prostate cancer confirmed on histology. 
  Results: We collected data on 318 cases of primary prostate cancer during the study period. Mean patient age was 72.7 years (Range: 49; 94 years). Family history of prostate cancer was found in 22 patients (6.91%). The average consultation time was 18.6 months. The circumstances of discovery were dominated by obstructive voiding disorders (97.16%). Digital Rectal examination was suggestive in 55.40% of patients. PSA level was above 20 ng/ml in 76.7% of patients. Prostatic adenocarcinoma was the only histological type (100%). Localized cancer represented 7.2% and locally advanced cancer occurred in 36.5% of cases, while metastatic cancer accounted for 56.3%. Radical prostatectomy was performed in 3.18% of cases. Mortality rate was estimated at 8.50% after 1 year. 
  Conclusion: Prostate cancer is the leading urological cancer in the Thies region. It is characterized by the predominance of locally advanced and metastatic forms.
 
</p></abstract><kwd-group><kwd>Prostate Cancer</kwd><kwd> Epidemiology</kwd><kwd> Histology</kwd><kwd> Metastasis</kwd><kwd> Mortality</kwd><kwd> Thies</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Prostate cancer (PCa) is the most common cancer in men over the age of 50 and represents the second cause of cancer death after bronchopulmonary cancer [<xref ref-type="bibr" rid="scirp.131239-ref1">1</xref>] , [<xref ref-type="bibr" rid="scirp.131239-ref2">2</xref>] . In Senegal it is the leading urological cancer [<xref ref-type="bibr" rid="scirp.131239-ref3">3</xref>] . The incidence is increasing due to the use of prostate-specific antigen (PSA) testing [<xref ref-type="bibr" rid="scirp.131239-ref3">3</xref>] . Its incidence is higher among African-Americans as well as in the French West Indies where the prevalence and mortality rates are higher than in metropolitan France [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] . PCa has traditionally been diagnosed by digital rectal examination (DRE) and prostate-specific antigen (PSA) blood test, followed by transrectal ultrasound (TRUS) guided biopsy. In Senegal this cancer is still diagnosed at a locally advanced or metastatic stage and few studies concerning screening have been carried out [<xref ref-type="bibr" rid="scirp.131239-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref8">8</xref>] . Prostate cancer remains the second leading cause of cancer mortality in men over 50 after lung cancer [<xref ref-type="bibr" rid="scirp.131239-ref1">1</xref>] . In Africa as in Senegal, data on prostate cancer are relatively rare. However, in Nigeria, Osegbe et al. [<xref ref-type="bibr" rid="scirp.131239-ref9">9</xref>] in 1997 found a hospital incidence of 127 per 100,000 for an annual mortality of 20,000. The objective of this work was to describe the epidemiological, diagnostic and therapeutic particularities of prostate cancer in the Thies region.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>We carried out a descriptive study between January 1<sup>st</sup>, 2015 to December 31<sup>st</sup>, 2020 in the different hospitals in the Thies region: Public hospitals of Thies, Mbour, Tivaouane and Saint Jean de Dieu hospital. Data were collected from patient medical records, hospitalization and pathology registries. The diagnosis of prostate cancer was established based on digital rectal examination data, total PSA level results and histological results of samples obtained from a series of prostate biopsy and adenomectomy or specimens of transurethral resection of the prostate (TURP). The extension assessment included a clinical examination, abdominal ultrasound, thoraco-abdominopelvic tomography (CT-TAP), standard radiography, bone scintigraphy. Staging was carried out according to the TNM 2016 classification. We also used the D’Amico cclassification. Treatment consisted of radical prostatectomy, hormonal therapy, and bilateral surgical pulpectomy. Patients were followed up every 3 months.</p><p>We included all patients followed for prostate cancer whose pathology examination confirmed by biopsy samples or surgical specimens. Excluded from this study are all cases of cancer occurring in people not living in the Thies region, recurrences or metastases of a cancer revealed before the study period.</p><p>The parameters studied were frequency, age of patients at diagnosis, family history of prostate cancer, clinical signs, DRE, total PSA blood test, pathology type, Gleason score, tumor stage, treatment and evolution after treatment.</p><p>Data entry and analysis were carried out using Word and Excel 2016 software.</p></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Epidemiological Results</title><sec id="s3_1_1"><title>3.1.1. Frequency of PCa</title><p>During the study period, we recorded 318 cases of prostate cancer out of a total of 478 urogenital cancers, with an average of 70.6 cases per year and a proportion of 87.4% of all urologic cancers. The largest number of cases (28.3%) was recorded during 2018 (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p></sec><sec id="s3_1_2"><title>3.1.2. Age Distribution of Patients</title><p>The average age of patients was 72.7 years (Age range 30 to 94 years). Of our cohort, patients under 50 ages at diagnosis represented 1.87% and 55% of them were over 70 years. The age group between 70 and 80 years was the most represented. <xref ref-type="fig" rid="fig2">Figure 2</xref> shows the representation of PCa cases according to age group (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p></sec></sec><sec id="s3_2"><title>3.2. Distribution of Prostate Cancers According to the diagnosis</title><p>A family history of prostate cancer was noted in 22 patients (6.91%).</p><p>Clinical features included lower urinary tract obstructive symptoms in 166 (52.2%), a urinary retention 75 (23.6%), a hematuria 96 (30.1%), bone pain 72 (22.64%). <xref ref-type="table" rid="table1">Table 1</xref> shows a distribution of PCa according to the circumstances of discovery. General condition was maintained in 41% of patients. On digital rectal examination (DRE), the prostate was suspicious of malignancy in the form of indurated, nodular or pelvic shielding appearance in 55.4% of patients. Total PSA was less than 10 ng/ml in 6.31% of patients and greater than 100 ng/ml in 35.53% of cases. <xref ref-type="table" rid="table1">Table 1</xref> shows a distribution of prostate cancers according to DRE and PSA results (N = 318).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Repartition of patients according to epidemiological, diagnosis results</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Mean age = 72, 7 years (age range = 30 - 94 years)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Risk factors</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Ethnicity (African people; black race)</td><td align="center" valign="middle" >318</td><td align="center" valign="middle" >100</td></tr><tr><td align="center" valign="middle" >History family of PCa</td><td align="center" valign="middle" >22</td><td align="center" valign="middle" >6.91</td></tr><tr><td align="center" valign="middle" >Circumstances of discovery</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Obstructive urinary disorders (Dysuria)</td><td align="center" valign="middle" >166</td><td align="center" valign="middle" >52.2</td></tr><tr><td align="center" valign="middle" >Frequency</td><td align="center" valign="middle" >131</td><td align="center" valign="middle" >42.45</td></tr><tr><td align="center" valign="middle" >urinary retention</td><td align="center" valign="middle" >75</td><td align="center" valign="middle" >23.6</td></tr><tr><td align="center" valign="middle" >Hematuria</td><td align="center" valign="middle" >96</td><td align="center" valign="middle" >30.1</td></tr><tr><td align="center" valign="middle" >Bone pain</td><td align="center" valign="middle" >72</td><td align="center" valign="middle" >22.64</td></tr><tr><td align="center" valign="middle" >Erectile dysfonction</td><td align="center" valign="middle" >41</td><td align="center" valign="middle" >12.9</td></tr><tr><td align="center" valign="middle" >Systematic discovery (operative specimen, resection shavings)</td><td align="center" valign="middle" >145</td><td align="center" valign="middle" >39.3</td></tr><tr><td align="center" valign="middle" >Results of digital rectal examination (DRE)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >DRE normal</td><td align="center" valign="middle" >37</td><td align="center" valign="middle" >11.6</td></tr><tr><td align="center" valign="middle" >DRE benign aspect</td><td align="center" valign="middle" >105</td><td align="center" valign="middle" >33</td></tr><tr><td align="center" valign="middle" >DRE suspect of malignacy</td><td align="center" valign="middle" >176</td><td align="center" valign="middle" >55.4</td></tr><tr><td align="center" valign="middle" >Total PSA testing (ng/ml)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&lt;10</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.3</td></tr><tr><td align="center" valign="middle" >10 - 20</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >6</td></tr><tr><td align="center" valign="middle" >21 - 50</td><td align="center" valign="middle" >111</td><td align="center" valign="middle" >34.9</td></tr><tr><td align="center" valign="middle" >51 - 100</td><td align="center" valign="middle" >72</td><td align="center" valign="middle" >22.6</td></tr><tr><td align="center" valign="middle" >100 - 1000</td><td align="center" valign="middle" >90</td><td align="center" valign="middle" >28.3</td></tr><tr><td align="center" valign="middle" >&gt;1000</td><td align="center" valign="middle" >23</td><td align="center" valign="middle" >7.23</td></tr><tr><td align="center" valign="middle" >Imaging</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Ultrasound</td><td align="center" valign="middle" >285</td><td align="center" valign="middle" >89.6</td></tr><tr><td align="center" valign="middle" >CT-Scan</td><td align="center" valign="middle" >251</td><td align="center" valign="middle" >78.9</td></tr><tr><td align="center" valign="middle" >MRI</td><td align="center" valign="middle" >02</td><td align="center" valign="middle" >0.6</td></tr><tr><td align="center" valign="middle" >Lombosacral spine X-ray</td><td align="center" valign="middle" >74</td><td align="center" valign="middle" >23.3</td></tr><tr><td align="center" valign="middle" >Bone scan</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >0.95</td></tr></tbody></table></table-wrap><p>The different imaging explorations carried out are summarized in <xref ref-type="table" rid="table1">Table 1</xref>. Technetium 99 bone scintigraphy was performed in 3 patients.</p></sec><sec id="s3_3"><title>3.3. Anatomopathological Results</title><p>Prostatic adenocarcinoma was the only histopathological type (100%). <xref ref-type="fig" rid="fig3">Figure 3</xref> shows a distribution of prostate cancers according to Gleason score (N = 318). Gleason score very high between 7 and 10. The tumor was well differentiated in 39.9% and poorly differentiated in 6.29% patients.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Reartition of patients according tumour stage, therapeutic modalities and evolution</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Frequencies</th><th align="center" valign="middle" >Pourcentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Tumour Stage</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Localized PCa</td><td align="center" valign="middle" >23</td><td align="center" valign="middle" >7.2</td></tr><tr><td align="center" valign="middle" >Localized low risk</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >4.08</td></tr><tr><td align="center" valign="middle" >Localized intermediate risk</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >3.18</td></tr><tr><td align="center" valign="middle" >Localized high risk</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >2.20</td></tr><tr><td align="center" valign="middle" >Locally advanced PCa</td><td align="center" valign="middle" >116</td><td align="center" valign="middle" >36.5</td></tr><tr><td align="center" valign="middle" >Metastatic PCa</td><td align="center" valign="middle" >179</td><td align="center" valign="middle" >56.3</td></tr><tr><td align="center" valign="middle" >Therapeutic aspects</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Radical Prostatectomy</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >3.18</td></tr><tr><td align="center" valign="middle" >Bilateral pulpectomy (surgery castration)</td><td align="center" valign="middle" >71</td><td align="center" valign="middle" >22.3</td></tr><tr><td align="center" valign="middle" >Antiandrogen</td><td align="center" valign="middle" >161</td><td align="center" valign="middle" >50.6</td></tr><tr><td align="center" valign="middle" >Bilateral Pulpectomy + Antiandrogen</td><td align="center" valign="middle" >23</td><td align="center" valign="middle" >7.25</td></tr><tr><td align="center" valign="middle" >LHRH analogue</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >4.75</td></tr><tr><td align="center" valign="middle" >Evolution (1 year)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Survival rate</td><td align="center" valign="middle" >291</td><td align="center" valign="middle" >91.50</td></tr><tr><td align="center" valign="middle" >Mortality rate</td><td align="center" valign="middle" >27</td><td align="center" valign="middle" >8.50</td></tr><tr><td align="center" valign="middle" >Local recurrence after prostatectomy</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >3</td></tr></tbody></table></table-wrap></sec><sec id="s3_4"><title>3.4. Tumor Stage and Therapeutic Modalities</title><p>At the end of the extension assessment and according to the 2016 cTNM classification, localized cancer represented 7.2% and locally advanced cancer occurred in 36.5% of cases, while metastatic cancer accounted for 56.3%. The locations of the metastases were bone (92.6%), visceral (19.8%) and lymph node (13.8%).</p><p>The urological management of PCa is reported in <xref ref-type="table" rid="table2">Table 2</xref>. Open radical prostatectomy was performed in 10 patients (3.18%). Bilateral orchiectomy alone was performed in 71 patients (22.32%) and in combination with anti-androgens in 23 patients (7.23%). LHRH agonists in combination with antiandrogens, to achieve complete androgen blockade, were used in 16 patients (5.03%). Castration resistance was observed in 26 patients (8.17%) of patients placed on hormonal therapy.</p><p>The overall survival rate was observed in 91.50% of patients after 1 year.</p></sec></sec><sec id="s4"><title>4. Discussion</title><sec id="s4_1"><title>4.1. Epidemiology</title><p>Prostate cancer is the second most common cancer in men worldwide with 1.4 million new cases worldwide [<xref ref-type="bibr" rid="scirp.131239-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref2">2</xref>] . In our series, the annual frequency was 70.6 cases and prostate cancer accounted for 87.4% for all urogenital cancers. In our region, prostate cancer ranks first among urogenital cancers. Osegbe et al. [<xref ref-type="bibr" rid="scirp.131239-ref9">9</xref>] reported a hospital-based incidence of 127 per 100,000.</p><p>However, in Europe, Prostate cancer is the most common cancer in men with an estimated number of 382,000 cases occurring during 2008 [<xref ref-type="bibr" rid="scirp.131239-ref10">10</xref>] . The highest incidence rate of prostate cancer was seen in Australia/New Zealand, in North America and the Caribbean and South Africa [<xref ref-type="bibr" rid="scirp.131239-ref1">1</xref>] .</p><p>Prostate cancer is the third leading cause of deaths from cancer in men. Prostate cancer is the third leading cause of death cancer in men and the mortality rate increases with age. The practice of early detection and the improvement of therapeutic management, particularly for metastatic forms of the disease, have contributed to the reduction in specific mortality due to PCa [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref10">10</xref>] .</p><p>The average age at diagnosis is currently 70 years [<xref ref-type="bibr" rid="scirp.131239-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] . In our study it was 72.7 years. Which is consistent with the age of predilection for prostate cancer as in most African, European and American series [<xref ref-type="bibr" rid="scirp.131239-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref10">10</xref>] . However, there is a significant difference in the average ages noted by other authors in Ghana, Togo and Burkina Faso who reported 60 years [<xref ref-type="bibr" rid="scirp.131239-ref11">11</xref>] - [<xref ref-type="bibr" rid="scirp.131239-ref16">16</xref>] .</p><p>Identified risk factors for CaP include age, ethnicity, and family history of prostate and breast cancer [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] . PCa is the most frequently diagnosed malignancy in elderly men [<xref ref-type="bibr" rid="scirp.131239-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref10">10</xref>] . It has been observed that the risk increases especially after age 40 in black men or men with a family history of prostate cancer and after age 50 in white men with no family history of prostate cancer [<xref ref-type="bibr" rid="scirp.131239-ref1">1</xref>] . The incidence of prostate cancer and mortality are twice as high in the French West Indies as in mainland France [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] . Hereditary and environmental factors are known to play some role in the genesis of PCa [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref17">17</xref>] . Additionally, 10% of hereditary PCa occur in relatively young patients [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref17">17</xref>] .</p></sec><sec id="s4_2"><title>4.2. Diagnosis</title><p>In our series, the circumstances of prostate cancer diagnosis were mainly represented by lower urinary tract symptoms (LUTS). For some authors, the existence of clinical signs in CaP reflects a locally advanced or metastatic stage [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] .</p><p>Palpation of irregularity or nodule during DRE still remains an indication for prostate biopsy regardless of the level of PSA [<xref ref-type="bibr" rid="scirp.131239-ref18">18</xref>] . In our study, DRE was suspicious of malignancy in 55.4% of cases and was an indication for prostate biopsy regardless of the PSA value. Niang et al. [<xref ref-type="bibr" rid="scirp.131239-ref19">19</xref>] found a suggestive EDR in 87% of patients followed for advanced prostate cancer. According Descott et al. [<xref ref-type="bibr" rid="scirp.131239-ref20">20</xref>] more than 60% of PCas are diagnosed in asymptomatic patients, with normal DRE and elevated PSA.</p><p>A high PSA greater than 20 n/ml was noted in a large proportion of patients. This corroborates data observed in the literature regarding African studies where patients had elevated total PSA levels at the time of diagnosis, which demonstrates the absence of early detection and screening policy for prostate cancer in our regions [<xref ref-type="bibr" rid="scirp.131239-ref11">11</xref>] - [<xref ref-type="bibr" rid="scirp.131239-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref23">23</xref>] . For Gueye et al. [<xref ref-type="bibr" rid="scirp.131239-ref3">3</xref>] as well as Cussenot et al. [<xref ref-type="bibr" rid="scirp.131239-ref24">24</xref>] , the high mean PSA level is correlated with the long course of the disease. For Niang et al. [<xref ref-type="bibr" rid="scirp.131239-ref19">19</xref>] , it is established that there is extra-prostatic involvement in 80% of cases for PSA values above 50 ng/mL.</p><p>Digital Rectal examination (DRE) and PSA measurement play a key role in the diagnosis of prostate cancer. In addition, this association makes it possible to detect cases of CaP early. Individual detection, based on fair and honest information of the patient, is based on the search for risk factors, digital rectal examination and PSA measurement, whereas screening consisting of systematically searching for a disease in an asymptomatic population remains controversial.</p><p>Prostatic adenocarcinoma was the only histological type in our series [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] . Ndoye et al. [<xref ref-type="bibr" rid="scirp.131239-ref25">25</xref>] reported a case of primary prostate sarcoma.</p><p>Ultrasound is not specific and is not sensitive for detecting CaP. It has no place in detection and staging [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] . It is used for post-void voiding assessment residual urine, prostate volume assessment and to guide biopsies [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref24">24</xref>] . Mutiparmetric MRI makes it possible to measure prostate volume; to describe each suspicious area (or target) identified and analyzed with the Prostate Imaging Reporting and Data System (PI-RADS) version available and to carry out the assessment of locoregional extension. However we do not have MRIs in hospitals in the Thies region [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] .</p></sec><sec id="s4_3"><title>4.3. Staging</title><p>A combination of DRE results, total PSA value and ISUP biopsy score improves the prediction of pT stage and lymph node spread [<xref ref-type="bibr" rid="scirp.131239-ref26">26</xref>] . Total PSA is correlated with the risk of metastasis, especially above 20 ng/ml [<xref ref-type="bibr" rid="scirp.131239-ref27">27</xref>] . In case of a locally advanced disease or lymph node or bone metastases, the thoraco-abdomino-pelvic CT scan remains useful to detect visceral metastases [<xref ref-type="bibr" rid="scirp.131239-ref28">28</xref>] . Also the number of positive biopsies is correlated with the risk of positive margins, extraprostatic extension and SV involvement [<xref ref-type="bibr" rid="scirp.131239-ref26">26</xref>] . Currently CT scanning is unnecessary if prostate MRI with lymph node acquisition is available. However, it remains indicated in cases of contraindication to MRI [<xref ref-type="bibr" rid="scirp.131239-ref29">29</xref>] . A nomogram associated with MRI data, biological data (PSA levels) and histological data of systematic and targeted biopsies can predict risk of lymph node extension and could avoid up to 60% of heals lymph nodes [<xref ref-type="bibr" rid="scirp.131239-ref30">30</xref>] . Whole body diffusion-weighted MRI allows a global evaluation of the skeleton and lymph node chains without irradiation or contrast product [<xref ref-type="bibr" rid="scirp.131239-ref31">31</xref>] . The performance of MRI is superior to scintigraphy coupled with standard radiography for identifying bone metastases and is identical to a CT scan for lymph node evaluation [<xref ref-type="bibr" rid="scirp.131239-ref31">31</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref32">32</xref>] . In our context of daily practice in the region of Thies, in Senegal we do not have MRI and bone scintigraphy. Furthermore, few patients are eligible for these means of diagnostic assistance due to a delay in treatment.</p><p>In our series the proportion of locally advanced and metastatic cancers remains high, reflecting the delay in treatment. Gueye et al. [<xref ref-type="bibr" rid="scirp.131239-ref3">3</xref>] diagnosed 40% of tumors at advanced stages.</p></sec><sec id="s4_4"><title>4.4. Treatment</title><p>According to the guidelines of the Cancerology Committee of the French Society of Urology (CCAFU), active surveillance (AS) must be based on the performance of a clinical examination, total PSA, MRI and a control biopsy is necessary 12 months after the start of the SA [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] . Also, it recommends stopping AS is indicated in the event of the appearance of a higher grade (ISUP 2 or higher) on control biopsies [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] .</p><p>The high prevalence of metastatic and locally advanced tumors in elderly patients reflects on the choice of our treatment and reduces the possibilities of radical surgical treatment. This explains on the one hand the low rate of radical prostatectomy (RP) performed in our series (3.18%), on the other hand the use of anti-androgen treatment. Radical prostatectomy (RP) can be offered to patients with low and intermediate risk PCA, depending on the co-morbidities and the life expectancy (&gt;10 years) [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref33">33</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref34">34</xref>] . Several authors have established the benefit of performing RP with extensive dissection, without preserving the nerve bands, in patients with high-risk or locally advanced CaP [<xref ref-type="bibr" rid="scirp.131239-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref33">33</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref35">35</xref>] . The indications are those for curative treatment of localised or locally advanced PCA. Lymphadenectomy includes bilateral excision of the ilio-obturator, internal iliac and external iliac lymph nodes up to the iliac bifurcation [<xref ref-type="bibr" rid="scirp.131239-ref36">36</xref>] [<xref ref-type="bibr" rid="scirp.131239-ref37">37</xref>] .</p><p>Currently in hospitals in the Thi&#232;s region, Senegal, we do not have radiotherapy or laparoscopy. However, as part of the multidisciplinary consultation, our patients are sometimes referred to Dakar which only has one radiotherapy center. In our study none of the patients had received radiotherapy.</p><p>Thus bilateral testicular pulpectomy (surgical castration) was the most used method in our series due to the low socio-economic level of our patients. Fall et al. [<xref ref-type="bibr" rid="scirp.131239-ref38">38</xref>] in Dakar as well as Diallo et al. [<xref ref-type="bibr" rid="scirp.131239-ref5">5</xref>] in Thies demonstrated the effectiveness of surgical castration which improves the clinical symptoms of patients. Surgical castration was also the most used treatment in the series of Kabor&#233; et al. [<xref ref-type="bibr" rid="scirp.131239-ref14">14</xref>] and Tengue et al. [<xref ref-type="bibr" rid="scirp.131239-ref15">15</xref>] with respectively 43.4% and 80.5% of testicular pulpectomy performed. Even if new generation hormone therapies have led to an improvement in symptoms and quality of life with good clinical and biological tolerance, in Africa as in Senegal, the use of medical hormone therapy is generally limited due to its high cost and its inaccessibility.</p><p>Survival is related to histopathologic feature, stage of disease and therapeutic response. In our study, the 1 year survival rate after treatment is 91.50%. Survival rates for prostate cancer are better in developed countries than in underdeveloped countries due to early detection of the disease.</p></sec></sec><sec id="s5"><title>5. Conclusion</title><p>Prostate cancer in the Thi&#232;s region of Senegal is the leading urological cancer. It is characterized by the predominance of locally advanced and metastatic forms; hence the need to encourage our populations to practice early detection of PCa and for health policy decision-makers to improve the diagnostic and therapeutic technical platform. The diagnosis of prostate cancer was late in our context, the treatment was limited by lack of resources; hence the need to improve the medical technical platform of hospitals.</p></sec><sec id="s6"><title>Ethical Considerations</title><p>A written informed consent was obtained for the publication of data and photos from patient.</p></sec><sec id="s7"><title>Author Contributions</title><p>All authors contributed to the development of this work. All authors read and approved the final version of the manuscript.</p></sec><sec id="s8"><title>Conflict of Interests</title><p>The authors declare that they have no conflict interest for this article.</p></sec><sec id="s9"><title>Cite this paper</title><p>Kouka, S.C.N., Bentefouet, L., Jalloh, M., Thiam, N.M., Faye, M., Diop, M., Cisse, M., Diame, A., Diallo, Y. and Sylla, C. (2024) Prostate Cancer in the Thies Region, Senegal: Epidemiological, Diagnostic and Therapeutic Aspects. Open Journal of Urology, 14, 71-82. https://doi.org/10.4236/oju.2024.142008</p></sec></body><back><ref-list><title>References</title><ref id="scirp.131239-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Siegel, R.L., Miller, K.D. and Jema, L.A. (2019) Cancer Statistics, 2019. CA: A Cancer Journal for Clinicians, 69, 7-34. https://doi.org/10.3322/caac.21551</mixed-citation></ref><ref id="scirp.131239-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Carioli, G., Bertuccio, P., Boffetta, P., Levi, F., La Vecchia, C., Negri, E., et al. (2020) European Cancer Mortality Predictions for the Year 2020 with a Focus on Prostate Cancer. Annals of Oncology, 31, 650-658. https://doi.org/10.1016/j.annonc.2020.02.009</mixed-citation></ref><ref id="scirp.131239-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Gueye, S.J.M., Labou, I., Niang, L., Kane, R. and Ndoye, M. (2004) Profil Clinique Du Cancer De La Prostate Au Sénégal. African Journal of Urology, 10, 203-207.</mixed-citation></ref><ref id="scirp.131239-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Rozet, F., Mongiat, P., Hennequin, C., et al. (2020) French CcAFU Guidelines— Update 2020-2022: Prostate Cancer. Progrés Urologie, 30, 136-251. https://doi.org/10.1016/S1166-7087(20)30752-1</mixed-citation></ref><ref id="scirp.131239-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Diallo, Y., Kouka, S.C., Jalloh, M., et al. (2019) Metastatic Prostate Cancer: Clinical Aspects and Therapeutic Management in the Region of Thies, Senegal. Medical &amp; Surgical Urology, 8, 224.</mixed-citation></ref><ref id="scirp.131239-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Gueye, S. (2014) Advanced Prostate Cancer in Senegal. Clinical Aspects at the General Hospital of Grand Yoff. Progrès en Urologie, 24, 271-275. https://doi.org/10.1016/j.purol.2013.08.317</mixed-citation></ref><ref id="scirp.131239-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Jalloh, M., Niang, L., Ndoye, M., Labou, I. and Gueye, S.M. (2013) Prostate Cancer in Sub Saharan Africa. Journal of Nephrology and Urology Research, 1, 15-20. https://doi.org/10.12970/2310-984X.2013.01.01.4</mixed-citation></ref><ref id="scirp.131239-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Cassell, A., Yunusa, B., Jalloh, M., et al. (2019) A Review of Localized Prostate Cancer: An African Perspective. World Journal of Oncology, 10, 162-168. https://doi.org/10.14740/wjon1221</mixed-citation></ref><ref id="scirp.131239-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Osegbe, D.N. (1997) Prostate Cancer in Nigerians: Facts and Non-Facts. Journal of Urology, 157, 1340-1343. https://doi.org/10.1016/S0022-5347(01)64966-8</mixed-citation></ref><ref id="scirp.131239-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Horwich, A., Parker, C., De Reijke, T., et al. (2013) Prostate Cancer: ESMO Clinical Practice Guidelines for Diagnosis, Treatment and Follow-Up. Annals of Oncology, 24, Vi106-Vi114. https://doi.org/10.1093/annonc/mdt208</mixed-citation></ref><ref id="scirp.131239-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Persaud, S., Goetz, L. and Burnett, A.L. (2017) Active Surveillance for Prostate Cancer: Is It Ready for Primetime in the Caribbean? African Journal of Urology, 23, 89-93. https://doi.org/10.1016/j.afju.2016.07.003</mixed-citation></ref><ref id="scirp.131239-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Kyei, M.Y., Mensah, E.J., Gepi-Attee, S., Kwami, D., Ampadu, K., Asante, E., Klufio, G.O., et al. (2013) Outcomes after Radical Prostatectomy in Ghanaians: A Surgeon’s Early Experience. ISRN Urology, 2013, Article ID: 832496. https://doi.org/10.1155/2013/832496</mixed-citation></ref><ref id="scirp.131239-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Ntama, A., Owon’Abessolo, P., Sango, A.J.F., Titti Mboumteke, J.G.F., Esson Mapoko, B.S., et al. (2023) épidémiologie et Diagnostic Du Cancer De La Prostate Dans La Ville De Douala (Cameroun). Health Sciences and Diseases, 24, 33-38. https://doi.org/10.4236/oju.2014.41002</mixed-citation></ref><ref id="scirp.131239-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Kabore, F.A., Zango, B., Kambou, T., Ouedraogo, A.S., Bam-Bara, A., Yameogo, C., et al. (2014) Prostate Cancer Disease Characteristics at the Time of Diagnosis and Initial Treatment Offered in a Tertiary Hospital at Ouagadougou (Burkina Faso). Open Journal of Urology, 4, 7-12.</mixed-citation></ref><ref id="scirp.131239-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Tengue, K., Kpatcha, T.M., Botcho, G., Leloua, E., Amavi, A.K., Sikpa, K., et al. (2016) Profil Epidemiologique, Diagnostique, Therapeutique et Evolutif Du Cancer De La Prostate Au Togo. African Journal of Urology, 22, 76-82. https://doi.org/10.1016/j.afju.2015.06.006</mixed-citation></ref><ref id="scirp.131239-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Ndiaye, M., Sow, O., Thiam, A., Sarr, A., Gaye, O. and Sine, B. (2020) Le Cancer De La Prostate Au Centre Hospitalier Universitaire Aristide Le Dantec De Dakar: Aspects épidémiologiques Sur Les Cinq Derniéres Années. Annales Africaines de Médecine, 14, e4004-e4009. https://anafrimed.net/cancer-de-la-prostate-au-centre-hospitalier-universitaire-aristidie-le-dantec-de-dakar-aspects-epidemiologiques-sur-les-cinq-dernieres-annees-prostate-cancer-in-aristide-le-dantec-hospital-of-dakar/</mixed-citation></ref><ref id="scirp.131239-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Xu, J. (2000) Combined Analysis of Hereditary Prostate Cancer Linkage to 1q24-25: Results from 772 Hereditary Prostate Cancer Families from the International Consortium for Prostate Cancer Genetics. The American Journal of Human Genetics, 66, 945-945. https://doi.org/10.1086/302807</mixed-citation></ref><ref id="scirp.131239-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Loeb, S. and Catalonia, W.J. (2009) What Is the Role of Digital Rectal Examination in Men Undergoing Serial Serum PSA Screening? Levels? Nature Clinical Practice Urology, 6, 68-69. https://doi.org/10.1038/ncpuro1294</mixed-citation></ref><ref id="scirp.131239-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Niang, L., Kouka, C.N., Jalloh, M. and Gueye, S.M. (2011) Screening for Prostate Cancer by Digital Rectal Examination and PSA Determination in Senegal. ISRN Oncology, 2011, Article ID: 943704. https://doi.org/10.5402/2011/943704</mixed-citation></ref><ref id="scirp.131239-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Descotes, J.L. (2019) Diagnosis of Prostate Cancer. Asian Journal of Urology, 6, 129-136. https://doi.org/10.1016/j.ajur.2018.11.007</mixed-citation></ref><ref id="scirp.131239-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Oranusi, C.K., Mbieri, U.T., Oranusi, I.O. and Nwofor, A.M. (2012) Prostate Cancer Awareness and Screening among Male Public Servants in Anambra State, Nigeria. African Journal of Urology, 18, 72-74. https://doi.org/10.1016/j.afju.2012.04.016</mixed-citation></ref><ref id="scirp.131239-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Nakandi, H., Kirabo, M., Semugabo, C., Kittengo, A., Ki-Tayimbwa, P., Kalungi, S. and Maena, J. (2013) Knowledge, Attitudes and Practices of Ugandan Men Regarding Prostate Cancer. African Journal of Urology, 19, 165-170. https://doi.org/10.1016/j.afju.2013.08.001</mixed-citation></ref><ref id="scirp.131239-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Fall, B., Sarr, A., Ouedraogo, B., Sow, Y., Thiam, A., Diallo, Y., et al. (2015) Detection Precoce Du Cancer De La Prostate Chez Des Apparentes De Premier Degre Au Senegal. African Journal of Urology, 21, 225-229. https://doi.org/10.1016/j.afju.2015.08.002</mixed-citation></ref><ref id="scirp.131239-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Cussenot, O. and Teillac, P. (1999) Cancer de la Prostate. Path Sciences, Paris, 616.</mixed-citation></ref><ref id="scirp.131239-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Ndoye, M., Niang, L., Gandaho, I.K., Jalloh, M., Labou, I. and Gueye, S.M. (2014) Cancer Avancé De La Prostate Au Sénégal. Aspects Diagnostiques á L’ho&amp;#770;pital De Grand Yoff. Progrés en Urologie, 24, 271-275. https://doi.org/10.1016/j.purol.2013.08.317</mixed-citation></ref><ref id="scirp.131239-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Eifler, J.B., Feng, Z., Brian, M., Partin, M.T., Humphreys, E.B., Misop, H., et al. (2013) An Updated Prostate Cancer Staging Nomogram (Partin Tables) Based on Cases from 2006 to 2011. BJU International, 111, 22-29. https://doi.org/10.1111/j.1464-410X.2012.11324.x</mixed-citation></ref><ref id="scirp.131239-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Salomon, L., Bastide, C., Beuzeboc, P., Cormier, L., Fromont, G., Hennequin, C., et al. (2013) CCAFU Recommendations 2013: Prostate Cancer. Progrès en Urologie, 23, S69-S101. https://doi.org/10.1016/S1166-7087(13)70048-4</mixed-citation></ref><ref id="scirp.131239-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">Rozet, F., Hennequin, C., Beauval, J.B., Beuzeboc, P., Cormier, L., Fromont-Hankard, G., et al. (2018) French CcAFU Guidelines—Update 2018-2020: Prostate Cancer. Progrès en Urologie, 28, R81-R132. https://doi.org/10.1016/j.purol.2019.01.007</mixed-citation></ref><ref id="scirp.131239-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">H&amp;#246;vels, A.M., Heesakkers, R.A., Adang, E.M., Jager, G.J., Strum, S., Hoogeveen, Y.L., et al. (2008) The Diagnostic Accuracy of CT and MRI in the Staging of Pelvic Lymph Nodes in Patients with Prostate Cancer: A Meta-Analysis. Clinical Radiology, 63, 387-395. https://doi.org/10.1016/j.crad.2007.05.022</mixed-citation></ref><ref id="scirp.131239-ref30"><label>30</label><mixed-citation publication-type="other" xlink:type="simple">Gandaglia, G., Ploussard, G., Valerio, M., Mattei, A., Fiori, C., Fossati, N., et al. (2019) A Novel Nomogram to Identify Candidates for Extended Pelvic Lymph Node Dissection among Patients with Clinically Localized Prostate Cancer Diagnosed with Magnetic Resonance Imaging-Targeted and Systematic Biopsies. European Urology, 75, 506-514. https://doi.org/10.1016/j.eururo.2018.10.012</mixed-citation></ref><ref id="scirp.131239-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Lecouvet, F.E., Simon, M., Tombal, B., Jamart, J., Vande Berg, B.C. and Simoni, P. (2010) Whole-Body MRI (WB-MRI) versus Axial Skeleton MRI (AS-MRI) to Detect and Measure Bone Metastases in Prostate. European Radiology, 20, 2973-2982. https://doi.org/10.1007/s00330-010-1879-3</mixed-citation></ref><ref id="scirp.131239-ref32"><label>32</label><mixed-citation publication-type="other" xlink:type="simple">Gutzeit, A., Doert, A., Froehlich, J.M., Eckhardt, B.P., Meili, A., Scherr, P., et al. (2010) Comparison of Diffusion-Weighted Whole Body MRI and Skeletal Scintigraphy for the Detection of Bone Metastases in Patients with Prostate or Breast Carcinoma. Skeletal Radiology, 39, 333-343. https://doi.org/10.1007/s00256-009-0789-4</mixed-citation></ref><ref id="scirp.131239-ref33"><label>33</label><mixed-citation publication-type="other" xlink:type="simple">Ruenes, A. and Gueye, S.M. (2008) Teaching Radical Prostatectomy in Sub-Saharan Africa. The Canadian Journal of Urology, 15, 3886-3889.</mixed-citation></ref><ref id="scirp.131239-ref34"><label>34</label><mixed-citation publication-type="other" xlink:type="simple">Babacar, S., Aissatou, B.N., Cyrille, Z.O., Amath, T., Alioune, S., Yaya, S., et al. (2018) Cancer de la Prostate Localisé à Haut Risque de Récidive: Résultats de la Prise Charge. African Journal of Urology, 24, 296-302. https://doi.org/10.1016/j.afju.2018.11.001</mixed-citation></ref><ref id="scirp.131239-ref35"><label>35</label><mixed-citation publication-type="other" xlink:type="simple">Niang, L., Ndoye, M., Ouattara, A., Jalloh, M., Labou, M., Thi-Am, I., Kouka, S.C., et al. (2013) Management of Prostate Cancer in Senegal: What Is Being Done? Progrès en Urologie, 23, 36-41. https://doi.org/10.1016/j.purol.2012.09.002</mixed-citation></ref><ref id="scirp.131239-ref36"><label>36</label><mixed-citation publication-type="other" xlink:type="simple">Sanda, M.G., Chen, R.C., Crispino, T., Freedland, S., Nelson, M.D., Reston, J., et al. (2017) Clinically Localized Prostate Cancer: AUA/ASTRO/SUO Guideline. Risk, 6, Article No. 27.</mixed-citation></ref><ref id="scirp.131239-ref37"><label>37</label><mixed-citation publication-type="other" xlink:type="simple">Heidenreich, A., Ohlmann, C.H. and Polyakov, S. (2007) Anatomical Extent of Pelvic Lymphadenectomy in Patients Undergoing Radical. European Urology, 52, 29-37. https://doi.org/10.1016/j.eururo.2007.04.020</mixed-citation></ref><ref id="scirp.131239-ref38"><label>38</label><mixed-citation publication-type="other" xlink:type="simple">Fall, B., Tengue, K., Sow, Y., Sarr, A., Ba, M. and Diagne, B.A. (2012) Place de la Pulpectomie Bilatérale Dans la Suppression Androgénique Pour Le Cancer de la Prostate. Progrès en Urologie, 22, 344-349. https://doi.org/10.1016/j.purol.2011.12.005</mixed-citation></ref></ref-list></back></article>