<?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">JCT</journal-id><journal-title-group><journal-title>Journal of Cancer Therapy</journal-title></journal-title-group><issn pub-type="epub">2151-1934</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jct.2017.811081</article-id><article-id pub-id-type="publisher-id">JCT-80283</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>
 
 
  Occurrence Delays of Metastatic Relapses of Breast Cancers Treated at University Hospital of Treichville (Abidjan-Cote d’Ivoire)
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Lydie</surname><given-names>Estelle Djanhan</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>Jean</surname><given-names>Marc Dia</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Boston</surname><given-names>Mian</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>Mouhideen</surname><given-names>Oyelade</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>Aboulaye</surname><given-names>Diallo</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>Privat</surname><given-names>Guié</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>Simplice</surname><given-names>Anongba</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Department of Gynecology and Obstetrics, University Hospital of Cocody, Abidjan, Cote d’Ivoire</addr-line></aff><aff id="aff1"><addr-line>Department of Gynecology and Obstetrics, University Hospital of Bouaké, Bouake, Cote d’Ivoire</addr-line></aff><aff id="aff2"><addr-line>Department of Gynecology and Obstetrics, University Hospital of Treichville, Abidjan, Cote d’Ivoire</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>jmlaminedia@yahoo.fr(JMD)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>07</day><month>11</month><year>2017</year></pub-date><volume>08</volume><issue>11</issue><fpage>924</fpage><lpage>932</lpage><history><date date-type="received"><day>4,</day>	<month>October</month>	<year>2017</year></date><date date-type="rev-recd"><day>10,</day>	<month>November</month>	<year>2017</year>	</date><date date-type="accepted"><day>13,</day>	<month>November</month>	<year>2017</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>
 
 
  Objective:
   Describe the occurrence delays of metastatic relapses of breast cancer based on the characteristics of the original tumor. <b>Methodology</b>: This is a retrospective and cohort study conducted from January 2000 to December 2015 on patients with metastatic
   
  relapse
   
  of breast cancer. <b>Results</b>: Out of 178 patients collected, the metastatic relapses were estimated at 49%, occurring in patients with an average age of 53.4 years.
   
  The majority of the patients was educated (91.6%) and did not have a high socioeconomic level (88.2%).
   
  The initial tumors were mainly at a clinical stage III (47.8%), SBR grade III (47.2%), high index Ki 67 (46.5%), negative RH (79.3%) and HER2 negative (58%).
   
  Metastases were unique in general (62.9%), dominated by bone locations (36.6%), with an average age of occurrence of 2.4 years.
   
  After the occurrence of these metastases, the cumulative survival rate was 5% at 3 years, and zero to 5 years. <b>Conclusion:</b> Metastatic relapses were common with poor prognosis.
 
</p></abstract><kwd-group><kwd>Breast Cancer</kwd><kwd> Risk Factors</kwd><kwd> Metastatic Relapses</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Breast cancer is the first cancer of woman in Cote d’Ivoire as in many countries of the world [<xref ref-type="bibr" rid="scirp.80283-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref2">2</xref>] , and its prognosis is closely related to the occurrence of metastases. Also after the curative treatment of non-metastatic forms, monitoring should be careful to quickly take care of locoregional and metastatic relapses that may occur. ASCO (American Society of Clinical Oncology) recommends clinical monitoring based on examination and clinical examination, every 4 months for 3 years, then every 6 months for the next 2 years, and once a year for the rest of life [<xref ref-type="bibr" rid="scirp.80283-ref3">3</xref>] . For additional examinations, only mammography and breast ultrasound should be performed annually, and other tests (chest x-ray, tumor markers, abdomino-pelvic ultrasound, bone scintigraphy, etc.) will be proposed only before functional signs [<xref ref-type="bibr" rid="scirp.80283-ref4">4</xref>] .<sup> </sup></p><p>In developing countries where there is no breast cancer screening program, the management of non-metastatic tumors is late, and exposes patients to high risk of metastatic relapse after initial treatment. Yet there are few publications on metastatic relapses in African literature.</p><p>This study was conducted with the objective to describe occurrence delays of metastatic relapses observed in our department.</p></sec><sec id="s2"><title>2. Methodology</title><p>This is a retrospective and cohort study conducted from January 2000 to December 2015 (16 years) in the gynecology department of the University Hospital of Treichville (CHUT).</p><p>It involved patients who benefited from a radical surgery with curative intent for nonmetastatic invasive breast cancer in our department between January 2000 and December 2010 and followed until December 2015.</p><p>These patients with non-metastatic invasive breast cancer have all initially benefited from a locoregional treatment and a systemic treatment. Locoregional treatment consisted in a total mastectomy, according to Patey, with axilary dissection by lack of radiotherapy and sentinel lymph nodes sampling. Regarding the systemic treatment, an adjuvant chemotherapy (FAC or FEC protocol) was performed in all patients, and only patients at Clinicalstage II and III received a neoadjuvant chemotherapy (same protocol) before surgery. At the end of the treatment and outside of any new event, the patients are followed according to ASCO recommendations.</p><p>We included in the study all patients who showed a metastatic breast cancer relapse during follow-up after initial treatment.</p><p>Patients operated outside our services, and those with breast cancer initially metastatic at initial diagnosis, were not included in the study.</p><p>Our data were collected on a survey patient records, chemotherapy registers, and anatomopathological findings.</p><p>The sample included 178 patients from whom the information was collected on a standard survey form. The analysis were done by the software Word, Excel, epi info and the statistical tests used were the calculations of the averages and frequencies.</p></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Epidemiological Characteristics</title><p>- Frequency of metastases</p><p>Between 2000 and 2010, 363 patients underwent radical breast cancer surgery and during surveillance until 2015, we found that 178 patients (49%) developed metastasis and we lost sight of 185 patients (51%) before the occurrence of metastases. The average follow-up duration was 3 years 7 months (extreme 9 months- 7 years 3 months) and cumulative survival without metastasis was 60% at 3 years and 43% at 5 years.</p><p>- Sociodemographic characteristics of patients</p><p>Patients had an average age of 53.4 years (extreme 38 - 74) and 62.4% were over 50 years of age, 91.6% were educated, and 88.2% did not have a high socio- economic level.</p></sec><sec id="s3_2"><title>3.2. Characteristics of Metastases</title><p>- Location of metastases</p><p>Metastases were unique in 112 patients (62.9%), dominated by osseous metastases (41 patients), lung (28 patients), liver (19 patients), hollow abdominal viscera (9 patients) and peritoneal (3 patients).</p><p>- Occurrencechronology of metastases</p><p>The average occurrence delay of metastases was 2.4 years (extreme 8 months - 7 years 6 months). And they occurred in less than 24 months in 84 patients (47.2%) and over 24 months in 94 patients (52.8%). At 5 years 95.4% of patients had metastases.</p><p>3-Relation between the prognostic factors of the initial tumor and the occurrence delay of metastases.</p></sec></sec><sec id="s4"><title>4. Discussion</title><sec id="s4_1"><title>4.1. Epidemiological Characteristics</title><p>- Frequency of metastases</p><p>Metastatic relapses were frequent in our study population, estimated at 49% with a cumulative survival rate without metastasis at 3 years of 60% (<xref ref-type="fig" rid="fig1">Figure 1</xref>). And this frequency seems underestimated given the high rate of loss of sight (51%) that we found. In African literature we have not found any articles estimating the frequency of metastatic relapses. On the other hand, in developed countries where the breast cancer management is performed earlier, and with a better technical equipment than in our countries, metastatic relapses are generally less frequent, estimated at less than 20% in ten years [<xref ref-type="bibr" rid="scirp.80283-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref7">7</xref>] . But it is important to question these figures, as even in these developed countries, in the late-patient population, there are high rates of metastatic relapse after mastectomy : greater than 50% in 10 years [<xref ref-type="bibr" rid="scirp.80283-ref8">8</xref>]</p><p>- Age</p><p>Our patients had an average age of 53.4 years and the majority (62.4%) was over 50 years of age (<xref ref-type="table" rid="table1">Table 1</xref>). In the literature, it is indeed reported that metastatic relapses are more frequent in women over 50 years of age, and locoregional relapses more frequent in younger women [<xref ref-type="bibr" rid="scirp.80283-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref10">10</xref>] . Menopausal status could affect the occurrence of these metastases, but the retrospective aspect of our study does not allow us to explore this parameter.</p><p>- Education level</p><p>The majority of our patients was educated (91.6%) (<xref ref-type="table" rid="table1">Table 1</xref>) and overall they had a sufficient level of education (secondary and higher) to better understand the interest of breast cancer screening. This screening would have permitted the management of the primary lesion at earlier stages, in order to limit the risk of metastatic relapses. But the absence of screening programs remains a reality in our regions, so that the notion of screening remains unknown to the population.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution of patients according to their socio-demographic characteristics</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Socio-demographic characteristics</th><th align="center" valign="middle" >Numbers</th><th align="center" valign="middle" >Frequency (%)</th></tr></thead><tr><td align="center" valign="middle" >Age (years)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >- &lt;40 years</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >4.5</td></tr><tr><td align="center" valign="middle" >- 40 - 50</td><td align="center" valign="middle" >59</td><td align="center" valign="middle" >33.1</td></tr><tr><td align="center" valign="middle" >- 50 - 60</td><td align="center" valign="middle" >63</td><td align="center" valign="middle" >35.4</td></tr><tr><td align="center" valign="middle" >- &gt;60</td><td align="center" valign="middle" >48</td><td align="center" valign="middle" >27</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >178</td><td align="center" valign="middle" >100</td></tr><tr><td align="center" valign="middle" >Level of education</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >- Not educated</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >8.4</td></tr><tr><td align="center" valign="middle" >- Primary</td><td align="center" valign="middle" >31</td><td align="center" valign="middle" >17.4</td></tr><tr><td align="center" valign="middle" >- Secondary</td><td align="center" valign="middle" >61</td><td align="center" valign="middle" >34.3</td></tr><tr><td align="center" valign="middle" >- Superior</td><td align="center" valign="middle" >71</td><td align="center" valign="middle" >39.9</td></tr><tr><td align="center" valign="middle" >- Total</td><td align="center" valign="middle" >178</td><td align="center" valign="middle" >100</td></tr><tr><td align="center" valign="middle" >Socio-economic level</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >- Low</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >7.3</td></tr><tr><td align="center" valign="middle" >- medium</td><td align="center" valign="middle" >144</td><td align="center" valign="middle" >80.9</td></tr><tr><td align="center" valign="middle" >- High</td><td align="center" valign="middle" >21</td><td align="center" valign="middle" >11.8</td></tr><tr><td align="center" valign="middle" >- Total</td><td align="center" valign="middle" >178</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><p>In a study conducted in our country on women having reached a secondary school level, Gui&#233; found that only 21% of women over 50 had already practiced breast cancer screening and in 42.1% of cases this screening went back to more than 4 years [<xref ref-type="bibr" rid="scirp.80283-ref11">11</xref>] .</p><p>- Socio-economic level</p><p>The patients in the study did not generally have a high socio-economic level (88.2%) (<xref ref-type="table" rid="table1">Table 1</xref>), constituting a real obstacle for the management of their disease (both the primary tumor and the metastases). In our country the management of cancers is expensive, and remains the responsibility of the patients because there is no social policy of health insurance. And in a study conducted in our country, Tour&#233; found that the lack of financial means caused the diagnostic delay of breast cancer in 36% of cases [<xref ref-type="bibr" rid="scirp.80283-ref1">1</xref>] .</p></sec><sec id="s4_2"><title>4.2. Characteristics of Metastases</title><p>- Location</p><p>We found that the majority of the metastases of our patients was unique (62.9%), and affected mainly bones, lung, liver, and brain. Several authors have also highlighted the high incidence of bone and lung forms [<xref ref-type="bibr" rid="scirp.80283-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref13">13</xref>] . As for Anhoux [<xref ref-type="bibr" rid="scirp.80283-ref14">14</xref>] he found, in his study conducted in our country, that the most common forms were pulmonary and hepatic. But we agree with the African authors who believe it is premature to conclude preferential locations in our conditions due to an underestimation related to insufficiency of paraclinical exploration: MRI and PET scan (Positron Emission Tomography) [<xref ref-type="bibr" rid="scirp.80283-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref15">15</xref>] .</p><p>- Occurrence delay of metastatic relapses</p><p>After the initial treatment of our patients, metastases occurred within an average delay of 2.4 years. At 24 months, almost half of the patients (47.2%) had metastases and at 5 years almost all patients (95.4%) had metastases. It is recognized that the majority of metastases occur within the first 5 years justifying an increased surveillance during this period [<xref ref-type="bibr" rid="scirp.80283-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref16">16</xref>] . But cases of late metastases occurring beyond 20 years have been reported, imposing also a long-term monitoring of all patients for breast cancer [<xref ref-type="bibr" rid="scirp.80283-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref18">18</xref>] .</p></sec><sec id="s4_3"><title>4.3. Relationship between the Prognostic Factors of the Initial Tumor and the Occurrence Delay of Metastases</title><p>1) Occurrence delay-Histological type of initial tumor</p><p>In our study 41.8% of patients having an invasive ductal carcinoma and 58.9% of patients who have had invasive lobular carcinoma, relapsed in less than 24 months (<xref ref-type="table" rid="table2">Table 2</xref>). In the literature, it is assumed that the histological type has no influence on prognosis : All invasive cancers have the same prognosis [<xref ref-type="bibr" rid="scirp.80283-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref20">20</xref>] .</p><p>2) Occurrence delay-initial stage of tumor</p><p>In the study, the majority of patients who relapsed within 24 had an advanced stage: II and III (<xref ref-type="table" rid="table2">Table 2</xref>). In the study of Anvo [<xref ref-type="bibr" rid="scirp.80283-ref21">21</xref>] in which it has identified all patients with metastasis, 52.5% of the population had an initial tumor at stage III. Carter and Host [<xref ref-type="bibr" rid="scirp.80283-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref23">23</xref>] have highlighted the pejorative role of the advanced</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Relation between the prognostic factors of the initial tumor and the occurrence delay of metastases</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Characteristics of the primary tumor</th><th align="center" valign="middle" >&lt;24 months</th><th align="center" valign="middle" >&gt; 24 months</th><th align="center" valign="middle" >Total</th></tr></thead><tr><td align="center" valign="middle" >Histological type</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >- IDC</td><td align="center" valign="middle" >51 (41.8%)</td><td align="center" valign="middle" >71 (58.2%)</td><td align="center" valign="middle" >122 (100%)</td></tr><tr><td align="center" valign="middle" >- ILC</td><td align="center" valign="middle" >33 (58.9%)</td><td align="center" valign="middle" >23 (41.1%)</td><td align="center" valign="middle" >56 (100%)</td></tr><tr><td align="center" valign="middle" >- Total</td><td align="center" valign="middle" >84</td><td align="center" valign="middle" >94</td><td align="center" valign="middle" >178</td></tr><tr><td align="center" valign="middle" >Clinical Stage</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >- I</td><td align="center" valign="middle" >7 (25%)</td><td align="center" valign="middle" >18 (72%)</td><td align="center" valign="middle" >25 (100%)</td></tr><tr><td align="center" valign="middle" >- II</td><td align="center" valign="middle" >25 (36.7%)</td><td align="center" valign="middle" >43 (63.3%)</td><td align="center" valign="middle" >68 (100%)</td></tr><tr><td align="center" valign="middle" >- III</td><td align="center" valign="middle" >52 (61.1%)</td><td align="center" valign="middle" >33 (38.9%)</td><td align="center" valign="middle" >85 (100%)</td></tr><tr><td align="center" valign="middle" >- Total</td><td align="center" valign="middle" >84</td><td align="center" valign="middle" >94</td><td align="center" valign="middle" >178</td></tr><tr><td align="center" valign="middle" >Grade SBR</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >- I</td><td align="center" valign="middle" >9 (2.9%)</td><td align="center" valign="middle" >22 (97.1%)</td><td align="center" valign="middle" >31 (100%)</td></tr><tr><td align="center" valign="middle" >- II</td><td align="center" valign="middle" >28 (44.4%)</td><td align="center" valign="middle" >35 (55.6%)</td><td align="center" valign="middle" >63 (100%)</td></tr><tr><td align="center" valign="middle" >- III</td><td align="center" valign="middle" >47 (55.9%)</td><td align="center" valign="middle" >37 (44.1%)</td><td align="center" valign="middle" >84 (100%)</td></tr><tr><td align="center" valign="middle" >- Total</td><td align="center" valign="middle" >84</td><td align="center" valign="middle" >94</td><td align="center" valign="middle" >178</td></tr><tr><td align="center" valign="middle" >Ki 67</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >- Low</td><td align="center" valign="middle" >6 (75%)</td><td align="center" valign="middle" >2 (25%)</td><td align="center" valign="middle" >8 (100%)</td></tr><tr><td align="center" valign="middle" >- Moderate</td><td align="center" valign="middle" >13 (56.5%)</td><td align="center" valign="middle" >10 (43.5%)</td><td align="center" valign="middle" >23 (100%)</td></tr><tr><td align="center" valign="middle" >- High</td><td align="center" valign="middle" >17 (62.9%)</td><td align="center" valign="middle" >10 (37.1%)</td><td align="center" valign="middle" >27 (100%)</td></tr><tr><td align="center" valign="middle" >- Total</td><td align="center" valign="middle" >36</td><td align="center" valign="middle" >22</td><td align="center" valign="middle" >58</td></tr><tr><td align="center" valign="middle" >HR</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >- Positive</td><td align="center" valign="middle" >3 (25%)</td><td align="center" valign="middle" >9 (75%)</td><td align="center" valign="middle" >12 (100%)</td></tr><tr><td align="center" valign="middle" >- Negative</td><td align="center" valign="middle" >38 (82.6%)</td><td align="center" valign="middle" >8 (17.4%)</td><td align="center" valign="middle" >46 (100%)</td></tr><tr><td align="center" valign="middle" >- Total</td><td align="center" valign="middle" >41</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >58</td></tr><tr><td align="center" valign="middle" >HER2</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >- Positive</td><td align="center" valign="middle" >8 (38.1%)</td><td align="center" valign="middle" >13 (61.9%)</td><td align="center" valign="middle" >21 (100%)</td></tr><tr><td align="center" valign="middle" >- Negative</td><td align="center" valign="middle" >30 (81.1%)</td><td align="center" valign="middle" >7 (18.9%)</td><td align="center" valign="middle" >37 (100%)</td></tr><tr><td align="center" valign="middle" >- Total</td><td align="center" valign="middle" >38</td><td align="center" valign="middle" >20</td><td align="center" valign="middle" >58</td></tr></tbody></table></table-wrap><p>IDC: Infiltrating Ducta Carcinoma. ILC: Infiltrating Lobular Carcinoma. HR: Hormone Receptors. SBR: Scarff Bloom Richardson.</p><p>initial stage of the disease on the occurrence of relapses.</p><p>3) Occurrence delay-histological prognostic factors</p><p>Just as the initial stage of the disease, the usual histological prognostic factors govern the risk of metastatic relapse especially in the first 5 years following the initial curative treatment. [<xref ref-type="bibr" rid="scirp.80283-ref24">24</xref>] Thus the more the histological and prognostic grade SBR is high, the more relapses are frequent and precocious with a high mortality [<xref ref-type="bibr" rid="scirp.80283-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref26">26</xref>] . In our series, we effectively found that metastatic relapses were more common in patients who had a higher grade (<xref ref-type="table" rid="table2">Table 2</xref>).</p><p>Concerning the other prognostic factors whose diagnosis is performed by immunohistochemistry (Receptor hormonal, Ki67, HER2), they were explored in only 58 patients (32.6%) because the laboratories were not equipped to conduct this examination during the period of study. These examinations were carried out abroad (France) at costs beyond the reach of the majority of patients. However the majority of patients who made these examinations had tumors with negative hormone receptors, an index Ki 67 high, and over expressed HER2.</p><p>The role of these various factors on the prognosis is also well known. The tumors that do not express estrogen receptors (ER-) relapse more frequently in the first 5 years, and tumors having a high index Ki 67 have a worse prognosis compared to tumors with moderate or low index [<xref ref-type="bibr" rid="scirp.80283-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref28">28</xref>] . Moreover the HER2 overexpression is a poor prognostic factor especially for N + patients, and high grade SBR [<xref ref-type="bibr" rid="scirp.80283-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.80283-ref30">30</xref>] .</p></sec></sec><sec id="s5"><title>5. Conclusion</title><p>Our study has shown us that the management of breast cancer poses enormous problems. Metastases occurred early after the initial treatment. For the improvement of the survival of patients with breast cancer, we must popularize screening sessions and early diagnosis in developing countries.</p></sec><sec id="s6"><title>Cite this paper</title><p>Djanhan, L.E., Dia, J.M., Mian, B., Oyelade, M., Diallo, A., Gui&#233;, P. and Anongba, S. (2017) Occurrence Delays of Metastatic Relapses of Breast Cancers Treated at University Hospital of Treichville (Abidjan-Cote d’Ivoire). Journal of Cancer Therapy, 8, 924-932. https://doi.org/10.4236/jct.2017.811081</p></sec></body><back><ref-list><title>References</title><ref id="scirp.80283-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Toure, M., Nguessan, E., Bambara, A.T., Kouassi, Y.K.K., Dia, J.M.L. and Adoubi, I. (2013) Factorslinked to Late Diagnosis in Breast Cancer in Sub-Saharan Africa: Case of Cote d’Ivoire. Gynécologie Obstétrique et Fertilité, 41, 696-700.  
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