<?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">OJOG</journal-id><journal-title-group><journal-title>Open Journal of Obstetrics and Gynecology</journal-title></journal-title-group><issn pub-type="epub">2160-8792</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojog.2023.138115</article-id><article-id pub-id-type="publisher-id">OJOG-127165</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>
 
 
  Immuno-Histochemical Profile of Breast Cancers at the General Hospital of Douala-Cameroon
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ekono</surname><given-names>Michel Roger Guy</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>Ngaha</surname><given-names>Yaneu Junie</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>Neng</surname><given-names>Humphry Tatah</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>Messakop</surname><given-names>Yannick</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>Azoumbou</surname><given-names>Mefant Thérèse</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>Ze</surname><given-names>Ngbwa Mimi Flore</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>Essome</surname><given-names>Henri</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>Essola</surname><given-names>Basile</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>Engbang</surname><given-names>Jean-Paul</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>Tchente</surname><given-names>Nguefack Charlotte</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Faculty of Health Sciences, University of Buea, Buea, Cameroon</addr-line></aff><aff id="aff1"><addr-line>Department of Obstetrics and Gynecology, Ebolowa Regional Hospital, Ebolowa, Cameroon</addr-line></aff><aff id="aff2"><addr-line>Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon</addr-line></aff><pub-date pub-type="epub"><day>08</day><month>08</month><year>2023</year></pub-date><volume>13</volume><issue>08</issue><fpage>1377</fpage><lpage>1388</lpage><history><date date-type="received"><day>14,</day>	<month>July</month>	<year>2023</year></date><date date-type="rev-recd"><day>20,</day>	<month>August</month>	<year>2023</year>	</date><date date-type="accepted"><day>23,</day>	<month>August</month>	<year>2023</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: The aim of the study was to describe the immunohistochemical aspects of breast cancers at Douala General Hospital
  ,
   Cameroon. Methodology: This was a descriptive study with retrospective data collection, conducted from January 1<sup>st</sup> 2010 and December 31<sup>st</sup> 2019. It was focused on histologically proven breast cancers followed up at Douala General Hospital. Results: We collected 285 cases of breast cancer, all female, representing an annual frequency of 28.5 cases. The mean age of the patients was 48
   
  &#177;
   
  13 years. The most frequent histological form was infiltrating ductal carcinoma (83.9%), with grade II predominating (38.6%). Immunohistochemical analyses were performed on 89 patients (31.23%). The triple-negative subtype was the most common class (35.95%), followed by Luminal A (32.60); Human Epidermal Receptor 2-class and Luminal B tumors were observed at a frequency of 13.48% each. Treatment consisted mainly of surgery (78.60%) combined with chemotherapy (65.97%) and/or radiotherapy (63.16%). Hormonal treatment was used in only 10.18% of patients. Targeted therapy was exceptional (4%). Conclusion: Triple-negative phenotype is the most common. However, potentially hormone-sensitive tumors account for almost half of all patients, who are relatively young. Individualized treatments are rare. It is important to systematize these analyses for all breast cancers, with a view to appropriate management in our environment.
 
</p></abstract><kwd-group><kwd>Breast Cancer</kwd><kwd> Immunohistochemistry</kwd><kwd> Douala General Hospital of Cameroon</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Breast cancer is the most common cancer worldwide [<xref ref-type="bibr" rid="scirp.127165-ref1">1</xref>] . In fact, the World Health Organization estimates that there will be 2.3 million new cases in 2020. It also carries a high mortality rate, with 685,000 deaths worldwide in the same year [<xref ref-type="bibr" rid="scirp.127165-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref2">2</xref>] . In Africa, the incidence of breast cancer has almost doubled in a decade [<xref ref-type="bibr" rid="scirp.127165-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref4">4</xref>] . In Cameroon, 4170 new cases were diagnosed in 2020, compared with 3265 in 2018 [<xref ref-type="bibr" rid="scirp.127165-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref4">4</xref>] . What’s more, the continent has a singularly high mortality rate. Along with Polynesia, Africa has the highest breast cancer mortality rate: 85,800 women died of the disease in 2020, while 2108 died in Cameroon in the same year [<xref ref-type="bibr" rid="scirp.127165-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref2">2</xref>] . However, the survival of breast cancer patients worldwide has improved markedly thanks to the introduction of new prognostic factors in the development of therapeutic strategies [<xref ref-type="bibr" rid="scirp.127165-ref5">5</xref>] . Indeed, several authors have demonstrated the role of tumor biology profiling, through immunohistochemistry, molecular biology and genomic studies, leading to personalized treatment for patients, which in turn guarantees better yields [<xref ref-type="bibr" rid="scirp.127165-ref5">5</xref>] - [<xref ref-type="bibr" rid="scirp.127165-ref9">9</xref>] . Immunohistochemical analysis of breast cancer is not yet widespread in Cameroon, and data on the subject remain limited. The aim of this study was to describe the immunohistochemical profile of breast cancer patients at the Douala General Hospital in Cameroon.</p></sec><sec id="s2"><title>2. Participant and Method</title><sec id="s2_1"><title>2.1. Setting and Study Population</title><p>This was a descriptive study with retrospective data collection from January 1er 2010 to December 31 2019, i.e. 9 years, at the Douala General Hospital. It concerned all patients followed in the obstetrics and gynecology department for histologically proven breast cancer. We excluded records of patients with primary cancer of another organ with metastasis to the breast and those with cancer other than gynecological or breast cancer.</p></sec><sec id="s2_2"><title>2.2. Procedures</title><p>Records of patients treated for breast cancer were identified in the outpatient, inpatient and operating room registers of the obstetrics and gynecology departments, and in the oncology department. We selected those in which the diagnosis had been confirmed by histological study, either on biopsy samples or surgical specimens. The medical record was consulted to collect data on a survey form previously designed using Epi Infos 7.0 software, including:</p><p>&#183; Epidemiological data: age, marital status.</p><p>&#183; Clinical data: personal history: medical, gynecological and obstetrical, toxicological, family history of cancer, lesion location, lesion sites, evolutionary stage (FIGO International Federation of Gynecology and Obstetrics) histological type, scarff Bloom Richardson’s histopronostic grade.</p><p>&#183; Histological data.</p><p>&#183; Immunohistochemical data.</p><p>We assessed estrogen receptor (ER) and progesterone receptor (PR) expression by the percentage of tumor cell nuclear labeling, estimated visually. A percentage greater than 1% was considered positive [<xref ref-type="bibr" rid="scirp.127165-ref10">10</xref>] . The results of RO and RP labeling were combined and analyzed jointly to define hormone receptor (HR) status. We defined RH-, any tumor with RO- and RP-status. HER (Human Epidermal Receptor) 2 expression was expressed as a score (0, 1+, 2+, 3+). A score of 0 or 1+ and a score of 3+ were considered HER2- and HER2-enriched, respectively. We considered 2+ scores as unclassifiable breast cancers. We proceeded to characterize molecular subtypes using the recommendations of the 13&#232;me St Gallen International Breast Cancer Conference 2011 [<xref ref-type="bibr" rid="scirp.127165-ref11">11</xref>] . Based on the expression of oetrogen receptor (OR), progesterone receptor (PR) genes, the level of proliferation index</p><p>Ki67 &lt; 14% = weak; Ki67 &gt; 14% = strong</p><p>and the expression of the proto-oncogene Human Epidermal Receptor 2 (HER2), patients were grouped into 4 subtypes:</p><p>Luminal type A Luminal type B HER 2 type.</p><p>And the basal like triple-negative type (see <xref ref-type="table" rid="table1">Table 1</xref>).</p></sec><sec id="s2_3"><title>2.3. Statistical Analysis</title><p>Data was entered and analyzed using SPSS 20.0 software. Qualitative data were represented as numbers and proportions. Quantitative data was represented by mean and standard deviation.</p></sec><sec id="s2_4"><title>2.4. Ethics</title><p>Ethical clearance was given by the institutional ethic committee of University of Douala. Total confidentiality was respected. All analyses were performed anonymously.</p></sec></sec><sec id="s3"><title>3. Results</title><p>During our study period, we recorded 285 cases of breast cancer, representing an annual frequency of 28.5 cases.</p><sec id="s3_1"><title>3.1. Epidemiological Data</title><p>All patients were female. The mean age of patients was 48 &#177; 13 years, with extremes of 19 and 84 years, and a median age of 47 years. The most represented age group was [40 - 50[ (30.9%), followed by [30 - 40[ (24.60%). Two-thirds of</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Molecular classification of breast cancers</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Criteria</th><th align="center" valign="middle" >Luminal A</th><th align="center" valign="middle" >Luminal B</th><th align="center" valign="middle" >HER 2</th><th align="center" valign="middle" >Basal-like Triple negative</th></tr></thead><tr><td align="center" valign="middle" >Immunohistochemistry</td><td align="center" valign="middle" >RO+/RP+/HER2-Ki67 &lt; 14%</td><td align="center" valign="middle" >RO+/RP+/HER2+ OR RO+/RP+/HER2-Ki67 &gt; 14%</td><td align="center" valign="middle" >RO-/RP-HER2+</td><td align="center" valign="middle" >RO-RP-HER2-</td></tr></tbody></table></table-wrap><p>patients were married (66.0%) (see <xref ref-type="table" rid="table2">Table 2</xref>).</p></sec><sec id="s3_2"><title>3.2. Clinical Data</title><p>A family history of breast cancer was found in 7.02%. Nearly half the patients (48.77%) were grand multiparous. More than half the patients (54.04%) were non-menopausal. The average consultation time was 8.9 &#177; 12.7 months. The predominant tumour location was the upper-external quadrant (41.8%), with left breast involvement predominating (53.3%). Stages III (54.73%) and II (36.49%) were the most common (see <xref ref-type="table" rid="table3">Table 3</xref> and <xref ref-type="table" rid="table4">Table 4</xref>).</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Ages, sex, marital status of patients. N = 285</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Terms and condition</th><th align="center" valign="middle" >Features</th><th align="center" valign="middle" >Values</th></tr></thead><tr><td align="center" valign="middle"  rowspan="2"  >Gender</td><td align="center" valign="middle" >Female</td><td align="center" valign="middle" >285 (100)</td></tr><tr><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle"  rowspan="2"  >Age</td><td align="center" valign="middle" >Average age</td><td align="center" valign="middle" >48 &#177; 13</td></tr><tr><td align="center" valign="middle" >Median age</td><td align="center" valign="middle" >47</td></tr><tr><td align="center" valign="middle"  rowspan="6"  >Age ranges</td><td align="center" valign="middle" >[10 - 20[</td><td align="center" valign="middle" >1 (0.35)</td></tr><tr><td align="center" valign="middle" >[20 - 30[</td><td align="center" valign="middle" >10 (3.5)</td></tr><tr><td align="center" valign="middle" >[30 - 40[</td><td align="center" valign="middle" >70 (24.6)</td></tr><tr><td align="center" valign="middle" >[40 - 50[</td><td align="center" valign="middle" >88 (30.9)</td></tr><tr><td align="center" valign="middle" >[50 - 60[</td><td align="center" valign="middle" >64 (22.5)</td></tr><tr><td align="center" valign="middle" >≥60</td><td align="center" valign="middle" >52 (18.2)</td></tr><tr><td align="center" valign="middle"  rowspan="3"  >Marital status</td><td align="center" valign="middle" >Bride</td><td align="center" valign="middle" >188 (66.0)</td></tr><tr><td align="center" valign="middle" >Single</td><td align="center" valign="middle" >57 (20.0)</td></tr><tr><td align="center" valign="middle" >Widow</td><td align="center" valign="middle" >40 (14.0)</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Medical and surgical history of patients with breast cancer at Douala General Hospital. N = 285</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Terms and conditions</th><th align="center" valign="middle" >Features</th><th align="center" valign="middle" >Values</th></tr></thead><tr><td align="center" valign="middle" >Notion of familial cancer</td><td align="center" valign="middle" >Breast Collar Ovary Horn</td><td align="center" valign="middle" >20 (7.02) 3 (1.05) 3 (1.05) 1 (0.35</td></tr><tr><td align="center" valign="middle" >Parity</td><td align="center" valign="middle" >Parity not specified 0 children 1 to 2 children 3 to 4 children ≥5 children</td><td align="center" valign="middle" >9 (3.16) 20 (7.02) 30 (10.52) 87 (30.53) 139 (48.77)</td></tr><tr><td align="center" valign="middle" >Genital status</td><td align="center" valign="middle" >Non-menopausal Menopausal women</td><td align="center" valign="middle" >154 (54.04) 131 (45.96)</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Lesion location and stage of breast cancer on admission to Douala General Hospital. N = 285</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Terms and conditions</th><th align="center" valign="middle" >Features</th><th align="center" valign="middle" >Number (%)</th></tr></thead><tr><td align="center" valign="middle" >Lesion location</td><td align="center" valign="middle" >Bilateral Law Left</td><td align="center" valign="middle" >5 (1.75) 128 (44.92) 152 (53.33)</td></tr><tr><td align="center" valign="middle" >Lesion site</td><td align="center" valign="middle" >Bifocal Lower External Quadrant (IEQ) Inferior-internal quadrant (QII) Upper-external quadrant (QSE) Superior-internal quadrant (QSI) Retroareolar Whole breast</td><td align="center" valign="middle" >3 (1.05) 49 (17.20) 25 (8.77) 119 (41.75) 59 (20.70) 10 (3.51) 20 (7.02)</td></tr><tr><td align="center" valign="middle" >Progressive stage on admission</td><td align="center" valign="middle" >Stage 1 Stage 2 Stage 3 Stage 4 Undetermined</td><td align="center" valign="middle" >10 (3.51) 104 (36.49) 156 (54.74) 10 (3.51) 5 (1.75)</td></tr></tbody></table></table-wrap></sec><sec id="s3_3"><title>3.3. Data on Histological Type, Grade and Immunohistochemical Class</title><p>Infiltrating ductal carcinoma was the most common histological type (83.86%). These cancers were predominantly grade II (64.33%). Immunohistochemical analyses were carried out on 89 patients (31.23%); the majority of breast cancers were of triple-negative subtype (35.95%), followed by Luminal A (32.60); tumours of HER2 class and Luminal B were observed at a frequency of 13.48% each (<xref ref-type="table" rid="table5">Table 5</xref>).</p></sec><sec id="s3_4"><title>3.4. Therapeutic Modality</title><p>Surgery was performed on 224 patients (78.60%). Almost all surgeries were radical (93.75%). Chemotherapy was used in 65.97% of patients, and was generally neoadjuvant (90.4%). It was generally neoadjuvant (90.4%), and the most frequently used chemotherapy protocol was Paclitaxel combined with Cyclophosphamide and Doxorubicin (AC) (35.6%).</p><p>Radiotherapy was used in 180 patients (63.16%). Hormonal treatment was used in 29 patients (10.18%). Among our patients, 12 (4.21%) benefited from Trastuzumab-based targeted therapy (see <xref ref-type="table" rid="table6">Table 6</xref>).</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>In the course of this study, we recorded 285 cases of breast cancer, all involving female subjects, a result similar to that of Atenguena and al [<xref ref-type="bibr" rid="scirp.127165-ref12">12</xref>] . In a multicentre study, Enbang and al. found 2.40% of cases in men [<xref ref-type="bibr" rid="scirp.127165-ref13">13</xref>] .</p><p>The mean age of the patients was 48 &#177; 13 years. The age of the patients in our study is close to that reported by various African authors [<xref ref-type="bibr" rid="scirp.127165-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref15">15</xref>] .</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Distribution of breast cancers by histological type, grade and immunohistochemical class at Douala General Hospital. N = 285</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Modality</th><th align="center" valign="middle" >Number (%)</th></tr></thead><tr><td align="center" valign="middle" >Histology</td><td align="center" valign="middle" >Invasive ductal carcinoma</td><td align="center" valign="middle" >239 (83.86)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Invasive lobular carcinoma</td><td align="center" valign="middle" >15 (5.26)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Medullary carcinoma</td><td align="center" valign="middle" >12 (4.21)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Intracanal carcinoma</td><td align="center" valign="middle" >11 (3.86)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Mucinous carcinoma</td><td align="center" valign="middle" >6 (2.11)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Paget’s disease</td><td align="center" valign="middle" >1 (0.35)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Mesenchymal sarcoma</td><td align="center" valign="middle" >1 (0.35)</td></tr><tr><td align="center" valign="middle" >Grade</td><td align="center" valign="middle" >Evaluated</td><td align="center" valign="middle" >171 (60)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Not rated</td><td align="center" valign="middle" >114 (40)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Grade 1</td><td align="center" valign="middle" >17 (9.94)</td></tr><tr><td align="center" valign="middle" >Grade n = 171</td><td align="center" valign="middle" >Grade 2</td><td align="center" valign="middle" >110 (64.33)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Grade 3</td><td align="center" valign="middle" >44 (25.73)</td></tr><tr><td align="center" valign="middle" >Immunohistochemical</td><td align="center" valign="middle" >Not done</td><td align="center" valign="middle" >196 (68.77)</td></tr><tr><td align="center" valign="middle" >class</td><td align="center" valign="middle" >Fact</td><td align="center" valign="middle" >89 (31.23)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Human Epidermal Receptor</td><td align="center" valign="middle" >12 (13.48)</td></tr><tr><td align="center" valign="middle" >Class n = 89</td><td align="center" valign="middle" >2 (HER2)</td><td align="center" valign="middle" >29 (32.60)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >LUMINAL A</td><td align="center" valign="middle" >12 (13.48)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >LUMINAL B</td><td align="center" valign="middle" >32 (35.95)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Triple negative basal like</td><td align="center" valign="middle" >4 (4.49)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Uncategorized</td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><p>HER2: Human Epidermal Receptor 2; ACR: American college of radiology.</p><p>More than half of our patients (54.03%) were non-menopausal, in line with various sub-Saharan authors [<xref ref-type="bibr" rid="scirp.127165-ref13">13</xref>] - [<xref ref-type="bibr" rid="scirp.127165-ref17">17</xref>] . Breast cancer therefore occurs in relatively young patients, still subject to sex hormone stimulation. This detail could prove decisive when faced with a hormone-sensitive tumour.</p><p>The vast majority of our patients were either grand multiparous (48.77%) or multiparous (31.52%), a fact found by various authors in our area, in contradiction with the risk factor status accorded to nulliparity in the literature [<xref ref-type="bibr" rid="scirp.127165-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref20">20</xref>] .</p><p>We observed 7.01% family history of breast cancer in our patients, indicating the possibility of genetic transmission mentioned in the literature (5% - 10%). Data similar to that of Tchente (7.14%) [<xref ref-type="bibr" rid="scirp.127165-ref21">21</xref>] .</p><p>There is conflicting evidence in the literature as to the predominance of tumour location in one breast or the other [<xref ref-type="bibr" rid="scirp.127165-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref25">25</xref>] . In our series, the left breast was the most frequently affected (53.33%). Bilateral involvement has been described in proportions ranging from 1% to 11.1% in our setting [<xref ref-type="bibr" rid="scirp.127165-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref25">25</xref>] . It is thought to be associated with mutation of the BRCA1 and</p><table-wrap id="table6" ><label><xref ref-type="table" rid="table6">Table 6</xref></label><caption><title> Distribution of patients by type of treatment</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Terms and conditions</th><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Number (%)</th></tr></thead><tr><td align="center" valign="middle" >Surgery</td><td align="center" valign="middle" >Yes No</td><td align="center" valign="middle" >224 (78.60) 61 (21.40)</td></tr><tr><td align="center" valign="middle" >Type of surgery n = 224</td><td align="center" valign="middle" >Radicale Curator</td><td align="center" valign="middle" >210 (93.75) 14 (6.25)</td></tr><tr><td align="center" valign="middle" >Radiotherapy</td><td align="center" valign="middle" >Yes No Not specified</td><td align="center" valign="middle" >180 (63.16) 35 (12.28) 70 (24.56)</td></tr><tr><td align="center" valign="middle" >Chemotherapy</td><td align="center" valign="middle" >Yes No</td><td align="center" valign="middle" >188 (65.97) 97 (34.03)</td></tr><tr><td align="center" valign="middle" >Type of chemotherapy n = 188</td><td align="center" valign="middle" >Adjuvant</td><td align="center" valign="middle" >27 (9.6)</td></tr><tr><td align="center" valign="middle" >Protocol used</td><td align="center" valign="middle" >Neoadjuvant FAC AC+Paclitaxel AC FAC+Docetaxel Cisplatin Docetaxel FAC+Paclitaxel Paclitaxel Vinorelbine TC Doxorubicne + Docetaxel</td><td align="center" valign="middle" >161 (90.4) 36 (17.6) 73 (35.6) 50 (24.4) 28 (13.7) 1 (0.5) 5 (2.4) 3 (1.5) 5 (2.4) 2 (1.0) 1 (0.5) 1 (0.5)</td></tr><tr><td align="center" valign="middle" >Targeted therapy n = 12 Hormonal treatment (29)</td><td align="center" valign="middle" >Trastuzumab Tamoxifen Anastrozole Radical castration</td><td align="center" valign="middle" >12 (4.2) 23 (79.2) 5 (17.3) 1 (3.5)</td></tr></tbody></table></table-wrap><p>BRCA2 genes [<xref ref-type="bibr" rid="scirp.127165-ref26">26</xref>] . It was observed in 1.8% of patients in our series.</p><p>The tumor was located preferentially in the upper lateral quadrant (41.75%), in line with the literature [<xref ref-type="bibr" rid="scirp.127165-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref23">23</xref>] . On admission, stage III patients predominated (54.7%), followed by stage II (36.5%). Late diagnosis has been described in several African series [<xref ref-type="bibr" rid="scirp.127165-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref27">27</xref>] .</p><p>Invasive ductal carcinoma was the most frequent histological type, accounting for 83.89% of all cases, in agreement with Atenguena and al. (90%) and other authors [<xref ref-type="bibr" rid="scirp.127165-ref12">12</xref>] - [<xref ref-type="bibr" rid="scirp.127165-ref25">25</xref>] . Sarcomas were rare (0.35%), in line with the work of Echimane et al. [<xref ref-type="bibr" rid="scirp.127165-ref28">28</xref>] . Lymphoma was not observed, contrary to the work of Engbang and al [<xref ref-type="bibr" rid="scirp.127165-ref13">13</xref>] .</p><p>The predominant Scarff Bloom Richardson histopronostic grade was grade II (64.33%), followed by grade III (25.73%), data similar to those of Engbang et al. (60% and 20%) [<xref ref-type="bibr" rid="scirp.127165-ref13">13</xref>] .</p><p>The most common immunohistochemical class was the triple-negative subtype (35.95%). The predominance of this subtype was found by Atenguena and al. and Atangana and al. in two Cameroonian series at rates of 41.9% and 37.98% respectively [<xref ref-type="bibr" rid="scirp.127165-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref14">14</xref>] . Other series have also found this predominance of triple-negative tumours in African patients [<xref ref-type="bibr" rid="scirp.127165-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref31">31</xref>] . However, Western and North African series found a preponderance of luminal A breast cancer [<xref ref-type="bibr" rid="scirp.127165-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.127165-ref33">33</xref>] .</p><p>The second most frequent immunohistochemical class was the Luminal A subtype (32.60%). This is in agreement with the findings of Atangana and al. (36.06%) [<xref ref-type="bibr" rid="scirp.127165-ref14">14</xref>] . However, in the Atenguena and al. series, the HER2 subtype was more frequent than the 2 hormone-sensitive forms (Luminal A and Luminal B), at 25.3% versus 16.1% for both [<xref ref-type="bibr" rid="scirp.127165-ref12">12</xref>] . Engbang and al, in a series of 3044 cases involving 5 of the 10 regions of Cameroon, were only able to observe immunohistochemical analysis in 11 patients (0.36%) [<xref ref-type="bibr" rid="scirp.127165-ref13">13</xref>] . These aspects reflect the inadequate implementation of these analyses in our environment, probably due to the limited technical resources available. This could have a deleterious impact on the management of breast cancer in our environment, even increasing mortality. Indeed, several authors have demonstrated the decisive role of immunohistochemical profiling in therapeutic and prognostic terms, and its vital importance in improving the efficiency of breast cancer management [<xref ref-type="bibr" rid="scirp.127165-ref5">5</xref>] - [<xref ref-type="bibr" rid="scirp.127165-ref9">9</xref>] .</p><p>More than 3/4 of patients (78.60%) underwent surgery, mostly radical, while virtually all 2/3 received courses of chemotherapy (65.97%) and/or radiotherapy (63.16%). Hormonal treatment was used in only 10, 18% of patients despite the relatively high proportion of potentially hormone-sensitive tumors in genitally active subjects in our series (luminal A = 32.60%); luminal B = 13.48%), i.e. almost half the cases. Targeted treatment was exceptional (4%). This shows that the results of immunohistochemical analysis had very little influence on treatment in this series. However, the successful management of breast cancer in the West seems to be based on matching the treatment to the patient’s immunohistochemical class and hormonal situation, resulting in individualized treatments with reputable yield [<xref ref-type="bibr" rid="scirp.127165-ref5">5</xref>] . This is a step that needs to be taken in our field.</p></sec><sec id="s5"><title>5. Conclusion</title><p>Breast cancer is the most common malignant tumour in our environment. It occurs mainly in women of childbearing age. The most common histological type is invasive ductal carcinoma. The triple-negative phenotype is the most frequent in our series. However, potentially hormone-sensitive tumors account for almost half of all patients. It is important to introduce systematic immunohistochemical analysis for all cases of breast cancer, possibly with the support of the state. Broader studies, including gene mutation research, will be carried out to guide and individualize treatment protocols, with a view to optimal management of this pathology in our environment.</p></sec><sec id="s6"><title>6. Highlights</title><sec id="s6_1"><title>6.1. What Is Known</title><p>Breast cancer is the number one cancer in the world. It has a high mortality rate in Cameroon. There is very little data on immunohistochemical aspects in our environment.</p></sec><sec id="s6_2"><title>6.2. The Issue</title><p>The aim of the study was to clarify the immunohistochemical aspects of breast cancers at Douala General Hospital.</p></sec><sec id="s6_3"><title>6.3. Contribution of This Study</title><p>&#183; Breast cancer occurs in relatively young patients. In most cases, it is diagnosed at an advanced stage;</p><p>&#183; The triple-negative subtype is the most common in our sample; almost half of patients have a hormone-sensitive subtype.</p></sec><sec id="s6_4"><title>6.4. The Implications</title><p>We need to systematize immunohistochemical analyses in Cameroon, and adapt treatment to the molecular profile.</p></sec></sec><sec id="s7"><title>Authors’ Contributions</title><p>Study design: Nguefack Tchente. Data collection: Ekono Michel Editor: Ekono Michel.</p><p>Revewers: Ngaha Yaneu Junie, Neng Humphry Tatah, Messakop Yannick, Azoumbou Mefant Th&#233;r&#232;se, Essome Henri, Essola Basile, Engbang Jean-Paul.</p><p>Supervision: Nguefack Tchente.</p></sec><sec id="s8"><title>Conflicts of Interest</title><p>Authors declare no conflicts of interest.</p></sec><sec id="s9"><title>Cite this paper</title><p>Guy, E.M.R., Junie, N.Y., Tatah, N.H., Yannick, M., Th&#233;r&#232;se, A.M., Flore, Z.N.M., Henri, E., Basile, E., Jean-Paul, E. and Charlotte, T.N. (2023) Immuno-Histochemical Profile of Breast Cancers at the General Hospital of Douala-Cameroon. 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