<?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.2019.101008</article-id><article-id pub-id-type="publisher-id">JCT-90132</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>
 
 
  Primary Bladder Adenocarcinoma: A Five-Year Retrospective Clinicopathologic Study of 42 Cases in Egyptian NCI (2010-14)
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yahia</surname><given-names>Ismail</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>Amr</surname><given-names>Kamal</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>Osama</surname><given-names>Yousof</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>Neveen</surname><given-names>Tahoun</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rasha</surname><given-names>Allam</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Radiation Oncology and Nuclear Medicine Department, National Cancer Institute, Cairo University, Cairo, Egypt</addr-line></aff><aff id="aff1"><addr-line>Medical Oncology Department, National Cancer Institute, Cairo University, Cairo, Egypt</addr-line></aff><aff id="aff2"><addr-line>Surgical Oncology Department, National Cancer Institute, Cairo University, Cairo, Egypt</addr-line></aff><aff id="aff5"><addr-line>Department of Cancer Epidemiology and Biostatistics, National Cancer Institute, Cairo University, Cairo, Egypt</addr-line></aff><aff id="aff4"><addr-line>Pathology Department, National Cancer Institute, Cairo University, Cairo, Egypt</addr-line></aff><pub-date pub-type="epub"><day>03</day><month>01</month><year>2019</year></pub-date><volume>10</volume><issue>01</issue><fpage>97</fpage><lpage>116</lpage><history><date date-type="received"><day>7,</day>	<month>January</month>	<year>2019</year></date><date date-type="rev-recd"><day>20,</day>	<month>January</month>	<year>2019</year>	</date><date date-type="accepted"><day>23,</day>	<month>January</month>	<year>2019</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>
 
 
  <u><em>Aim</em></u>
  : Globally, primary adenocarcinoma
   
  (AC) accounts for only 0.5% - 2% of bladder cancer
   
  (BC). Bilharziasis predisposes to AC in ~10% of BC in endemic regions. The aim was to study the clinicopathologic characteristics of this rare entity and define prognostic elements influencing disease-free
   
  (DFS) &amp; overall survival
   
  (OS). <b><u>Patients</u><u> &amp; Methods</u></b>: A retrospective analysis of 42 cases of primary bladder AC presented to the National Cancer Institute of Egypt (NCI-E) during a five-year period (2010-2014), clinicopathologic profiles, management and survival were assessed. <b><u>Results</u><u>: </u></b>The mean age was 55.5 years &#177;
   
  9.77 with male predominance. Hematuria, bilharziasis &amp; urachal type experienced in 88%, 35.7% &amp; 4.8%,
   
  respectively. Radical surgery was employed in 64.3%. Metastatic disease (stageIVB) found in 14.3%, initially.
   
  Eleven patients
   
  (26.2%) received palliative chemotherapy for their advanced or metastatic disease, objective response rates
   
  (ORR) were 0% &amp; 100% for those received gemcitabine/platinum &amp; capecitabine/oxaliplatin, respectively. The 5-year DFS &amp; OS rates were 40.7
  %
   &amp; 27%, respectively.
   
  DFS was significantly enhanced in patients having GII, negative nodes
   
  (pN0) and absence of hydronephrosis (p = 0.001, 0.011 &amp; 0.047, respectively). Presentation with hematuria, pN0 &amp; stage II w
  as
   linked significantly with longer OS (p = 0.007,
   
  0.037 &amp; &lt; 0.001, respectively). Tumour grade &amp; clinical stage were independent prognostic factors affecting DFS &amp; OS, respectively
   on multivariate analysis
  . <b><u>Conclusions</u><u>:</u></b> Notable reduction in incidence of bladder AC in Egypt 
  is 
  mostly due to decline in bilharzial infection. Tumor grade &amp; clinical stage are independent prognostic factors for DFS &amp; OS, respectively. Still no agreement about the role of adjuvant radiotherapy or chemotherapy, however, protocols employed for colorectal cancer seem to be profitable in advanced and metastatic cases. Further larger scale studies are needed to define the hazard factors, molecular characterises and optimal management of this rare type of BC.
 
</p></abstract><kwd-group><kwd>Bladder Cancer</kwd><kwd> Primary</kwd><kwd> Adenocarcinoma</kwd><kwd> Bilharziasis</kwd><kwd> NCI</kwd><kwd> Egypt</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Bladder cancer (BC) positions as the ninth most successive malignant neoplasm globally [<xref ref-type="bibr" rid="scirp.90132-ref1">1</xref>] , by far most of patients (~90%) have transitional cell carcinoma (TCC) as the main histologic variant in the west, while squamous cell carcinoma (SCC) is more rampant in Africa where there is widespread of Schistosoma hematobium [<xref ref-type="bibr" rid="scirp.90132-ref2">2</xref>] . Primary adenocarcinoma (AC) of the urinary bladder is found in approximately 0.5% - 2% of all BC and ranks as the third most frequent subtype [<xref ref-type="bibr" rid="scirp.90132-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] . In Egypt, BC represents one of the major health problems with an overall relative frequency of 18.3% [<xref ref-type="bibr" rid="scirp.90132-ref6">6</xref>] . Primary AC histology was depicted in 3.8% of all BC cases during a twelve-year period pathology cancer registry (2000-2011) of NCI-E [<xref ref-type="bibr" rid="scirp.90132-ref7">7</xref>] .</p><p>Smoking is still the prominent hazard factor for TCC [<xref ref-type="bibr" rid="scirp.90132-ref8">8</xref>] , however, for AC subtype other conceivable risk factors have been depicted e.g. schistosomiasis predisposes to AC in up to one-tenth of all BC in endemic territories [<xref ref-type="bibr" rid="scirp.90132-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref10">10</xref>] and those with a diagnosis of bladder exstrophy who develop malignant bladder tumours have AC in nearly 90% of cases [<xref ref-type="bibr" rid="scirp.90132-ref11">11</xref>] . Pathologically, it is derived from the urothelial coating the bladder that demonstrates a pure glandular phenotype which exhibits different microscopic morphologic patterns [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] . Macroscopically, it may present as a papillary, sessile or ulcerating growth that usually originates from the posterior wall but also could be found in other locations in the bladder [<xref ref-type="bibr" rid="scirp.90132-ref11">11</xref>] , in contrast to TCC which tends to grow in a multifocal pattern, AC frequently presents as a single lesion [<xref ref-type="bibr" rid="scirp.90132-ref12">12</xref>] . Urachal AC originates from the urachal remnant [<xref ref-type="bibr" rid="scirp.90132-ref13">13</xref>] and represents around one-third of primary bladder AC [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] , it is usually found in the bladder vault as a solitary polypoidal lesion and usually grouped together with bladder AC because they have enormous likeness in their features as it exhibits the similar microscopic patterns described in AC with the mucinous subtype being the most frequently experienced [<xref ref-type="bibr" rid="scirp.90132-ref14">14</xref>] .</p><p>The diagnosis of primary bladder AC should be proposed after meticulous exclusion of secondary AC involving the bladder either by direct intrusion from the surrounding organs or by metastasis from a remote site as they occur more frequent than the former [<xref ref-type="bibr" rid="scirp.90132-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref15">15</xref>] , it is usually developed in the sixth or seventh decade of age with male dominance [<xref ref-type="bibr" rid="scirp.90132-ref16">16</xref>] and gross hematuria is the common presenting complaint followed by dysuria and mucusuria [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] . Nearly 33% of the patients have positive nodal involvement at initial presentation [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref18">18</xref>] . Patients with urachal type tend to present in a younger age than bladder AC with also male predominance, in addition to hematuria they might complain with other symptoms related to its anatomical location like umbilical discharge and lower abdominal pain [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref13">13</xref>] .</p><p>Radical cystectomy (RC) accompanied with pelvic lymph node dissection (PLND) is considered the treatment of choice as the highest proportion of the patients have a muscle-invasive disease at presentation, whereas for the minority with superficial disease; transurethral resection of the bladder tumour (TURBT) is often employed [<xref ref-type="bibr" rid="scirp.90132-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref20">20</xref>] . On the other side, the standard surgical approach for urachal tumours is en-bloc resection of the umbilicus, bladder vault and the urachal ligament [<xref ref-type="bibr" rid="scirp.90132-ref21">21</xref>] .</p><p>The value of radiation therapy whether in adjuvant or neoadjuvant setting is as yet conflicting as AC is generally considered as a radioresistant disease, the five-year survival was previously reported to be less than 20% in those managed with radiotherapy alone. Two studies showed no survival advantage for preoperative irradiation [<xref ref-type="bibr" rid="scirp.90132-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref23">23</xref>] , however, a retrospective study from Egypt exhibited a potential valuable role of adjuvant radiation after RC in diminishing the local recurrence rate with subsequent significant enhancement in DFS [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] .</p><p>Still, there are no standard chemotherapy guidelines for the treatment of primary AC of the bladder [<xref ref-type="bibr" rid="scirp.90132-ref24">24</xref>] and the usual cisplatin-based protocols that are utilized successfully for TCC demonstrated little advantage on AC [<xref ref-type="bibr" rid="scirp.90132-ref14">14</xref>] . Some researchers recommended that a flouropyrimidine-based regimen should be tried [<xref ref-type="bibr" rid="scirp.90132-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref26">26</xref>] . Applying the same rationale for preoperative chemotherapy in TCC, it might be a sensible option for patients with locally advanced primary AC as it could help in downstaging the tumour ahead to surgery, eliminating micrometastases, and may diminish regional and distant relapse [<xref ref-type="bibr" rid="scirp.90132-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref28">28</xref>] .</p><p>In respect to prognosis; the five-year survival rates for AC are commonly low running from 5% - 33% [<xref ref-type="bibr" rid="scirp.90132-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref29">29</xref>] . The aim of the current retrospective study is to evaluate the incidence, the clinicopathologic features, the treatment outcome and prognostic elements influencing survival for patients with primary bladder AC in NCI-E.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>This is a retrospective cohort study involving patients with a diagnosis of primary AC of the urinary bladder who were treated at the National Cancer Institute of Egypt (NCI-E) over a five-year period; between January, 2010 and December, 2014. There were a total of 3144 cases of BC retrieved from the medical records during the specified period. Eligibility criteria included: age ≥ 18 years, both genders, definite pathological diagnosis of AC of the urinary bladder whether by cystoscopic biopsy specimen or the whole bladder specimen after radical surgery, final clinical diagnosis of primary AC made after exclusion of secondary (metastatic) AC involving the bladder by: negative colonoscopy and by the use of immunohistochemistry (IHC)―when needed―to exclude extension or metastasis from other primaries. Exclusion criteria included cases with documented clinical diagnosis of metastatic (secondary) AC to the urinary bladder, cases who didn’t underwent lower GI endoscopy or suspicious cases that were not subjected to confirmatory IHC. A total of 42 cases out of the 3144 BC cases (1.3%) were found to satisfy the inclusion criteria, their archived medical charts and pathology slides were retrieved from the medical records and pathology departments, respectively. The medical charts were thoroughly revised and all the clinicodemographic data were extracted that included: age, sex, residency (urban or rural area), main presenting complaint, date of first diagnosis of a urinary bladder mass and the imaging modality used, date and results of cystoscopy, pathology of cystoscopic biopsy, tumour location within the bladder, tumour size and pattern of macroscopic growth, clinical stage at presentation, date and type of curative surgery, pathological TNM stage for the operable patients, date of relapse and its location, patients presenting with initially metastatic disease and the sites of metastasis, findings of exploration for patients with advanced disease, adjuvant therapy (chemotherapy or radiation therapy) given for radically resected patients, palliative chemotherapy or palliative radiation given for recurrent, advanced or metastatic patients, response to treatment, date and state of last follow up. Patients were retrospectively followed up till the end of May, 2018 (end of data collection).</p><p>For patients who underwent curative surgery; RC in male patients included removal of the bladder, prostate gland, seminal vesicles together with perivesical fat and peritoneal coverage, in addition to PLND. Anterior pelvic exenteration (APE) in females included removal of the bladder, perivesical fat, PLND, peritoneal coverage, uterus, ovaries, urethra and anterior vaginal wall as described in [<xref ref-type="bibr" rid="scirp.90132-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref30">30</xref>] . The two patients with urachal carcinoma underwent en-bloc resection of the umbilicus and urachal ligament in addition to partial cystectomy (PC) as described in [<xref ref-type="bibr" rid="scirp.90132-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref31">31</xref>] .</p><p>The pathologist in charge for this study retrieved and revised the H &amp; E slides for the 42 cases and according to WHO classification for tumours of the urinary bladder; the not-otherwise specified (NOS) subtype shows non-specific glandular growth, the enteric type intimately looks like AC of the colorectum, tumours that show plentiful extracellular mucin with malignant cells lying within the mucin lakes are classified as mucinous adenocarcinoma (MAC), the signet ring adenocarcinoma (SRAC) variant where the cells have high intracellular mucin content that pushes the nucleus to eccentric site of the cell and finally, the mixed pattern demonstrates a mixture of these aforementioned growth patterns [<xref ref-type="bibr" rid="scirp.90132-ref32">32</xref>] . Depth of tumour invasion (pT), nodal status (pN), grade of differentiation and other associated pathology like bilharziasis, cystitis glandularis, cystitis cystica, etc. were documented. Confirmatory IHC was used in one case for a male with pT4a invading the prostate, PSA was negative on the specimen excluding primary prostatic origin in addition to normal serum PSA.</p></sec><sec id="s3"><title>3. Statistical Methods</title><p>Data were analyzed using IBM SPSS advanced statistics (Statistical Package for Social Sciences), version 23 (SPSS Inc., Chicago, IL). Median and range or mean and standard deviation were used as appropriate for numerical data, while qualitative data were described as number and percentage. The relation between qualitative variables was examined by Chi-square (Fisher’s exact) test as appropriate. Kaplan-Meier method was done for survival analysis. The log rank test was applied for comparison between two survival curves. Cox regression model was done for multivariate analysis in order to test for independent prognostic effect of statistically significant variables on univariate level with calculating hazard ratio and its 95% confidence interval. Bonferonni corrections of p value were done to avoid hyperinflation of type I error which arises from multiple testing. A p-value ≤ 0.05 was counted as statistically significant. All tests were two tailed. Overall survival (OS) was calculated from the date of diagnosis till the date of death or last follow up. Disease-free survival (DFS) was calculated from the date of curative surgery till the date of local or distant relapse, death or last follows up.</p></sec><sec id="s4"><title>4. Ethical Issues</title><p>No exposure to any hazards for the patients on this retrospective study. Presentation and gathering of data were absolutely anonymous with maintaining privacy and confidentiality to the maximum possible standards.</p></sec><sec id="s5"><title>5. Results</title><p>A cohort of 42 cases of primary AC of the urinary bladder, their mean age was 55.5 years &#177;9.77, median: 57 years (range: 29 - 68), with male predominance (64.3%) and Male: Female 1.8:1. The majority (69%) were resident in rural areas in Egypt. Hematuria was the most commonly reported presenting complaint in 88% of the patients. The method of initial diagnosis for detection of a bladder mass was ultrasound (U/S) of abdomen and pelvis in half of the patients whereas computed tomography (CT) was carried out in the remaining half. Different degrees of hydronephrosis were detected on initial imaging in more than half of the patients (52.4%). All the patients underwent baseline diagnostic cystoscopy, the most rampant pattern of tumour growth grossly was fungating/exophytic in 83.3% while the remaining 16.7% had ulcerative lesions with median tumour size 5 cm (range: 2 - 20). Posterior wall of the bladder was the most frequent location of the tumours in 57% followed by the dome in 19% whereas urachal type was encountered in just two patients (4.8%). Microscopically, AC-NOS was the pervasive histologic variant in 76.2% (<xref ref-type="fig" rid="fig1">Figure 1</xref>(a)), bilharziasis was found in addition to the bladder tumour in 15 patients (35.7%, <xref ref-type="fig" rid="fig1">Figure 1</xref>(b)) with 93% of those patients were resident in rural areas, whereas MAC (<xref ref-type="fig" rid="fig1">Figure 1</xref>(c)) and SRAC (<xref ref-type="fig" rid="fig1">Figure 1</xref>(d)) were found in 14.3% and 9.5%, respectively, with grade II differentiation depicted in the majority (78.6%). Clinical diagnosis of muscle-invasive disease (cT2) was detected whether by cystoscopy, imaging or bimanual examination under anaesthesia (EUA) in more than three quarters of</p><p>the patients (76%), whereas cT3b (gross extravesical extension) in 16.7%. Clinical assessment of lymph node status by imaging and examination revealed clinically negative nodes (cN0) in most of the patients (92%), consequently; by applying the AJCC staging 8th edition [<xref ref-type="bibr" rid="scirp.90132-ref33">33</xref>] ; initial clinical staging for the whole cohort showed that stage II was the most common in almost two thirds of the patients (66.7%) followed by clinical stage III and IVA in 16.7% and 2.3%, respectively, whereas distant metastatic disease at presentation (stage IVB) was anticipated in 6 patients (14.3%) with peritoneal nodules being the commonest site of metastasis in almost 67% of the metastatic patients (<xref ref-type="table" rid="table1">Table 1</xref>). On exploration; 6 patients had inoperable disease due to the presence of peritoneal nodules, fixed pelvic lymph nodes and fixed uterine invasion in 3, 2 &amp; 1 patients, respectively, whereas curative surgery was successful in 27 patients (64.3%) with RC being the most common radical surgery employed in 19 patients followed by APE and PC in 5 and 3 cases, respectively, pT3 was the prevalent stage in 15 patients followed by pT2 &amp; pT4 in 9 &amp; 3 patients, respectively, pathologically positive lymph node was found in only18.5% of cases (<xref ref-type="table" rid="table1">Table 1</xref>).</p><table-wrap-group id="1"><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Clincopathologic profiles of 42 cases of primary bladder adenocarcinoma</title></caption><table-wrap id="1_1"><table><tbody><thead><tr><th align="center" valign="middle" >Age (years): Mean &#177; SD Median (range)</th><th align="center" valign="middle" >55.5 &#177; 9.77 57 (29 - 68)</th></tr></thead><tr><td align="center" valign="middle" >Gender: Male Female</td><td align="center" valign="middle" >n (%) 27 (64.3) 15 (35.7)</td></tr><tr><td align="center" valign="middle" >Residency: Urban Rural</td><td align="center" valign="middle" >n (%) 13 (31) 29 (69)</td></tr><tr><td align="center" valign="middle" >Main presenting complaint: Hematuria Lower abdominal pain Dysuria Urgency Necroturia</td><td align="center" valign="middle" >n (%) 37 (88.1) 2 (4.8) 1 (2.4) 1 (2.4) 1 (2.4)</td></tr><tr><td align="center" valign="middle" >Methods of initial diagnosis: Non-Invasive (Imaging): US CT Invasive: Cystoscopy</td><td align="center" valign="middle" >n (%) 21 (50) 21 (50) 42 (100)</td></tr><tr><td align="center" valign="middle" >Tumour size (cm): Median (range)</td><td align="center" valign="middle" >5 (2 - 20)</td></tr><tr><td align="center" valign="middle" >Tumour growth pattern grossly: Fungating/Exophytic Ulcerative</td><td align="center" valign="middle" >n (%) 35 (83.3) 7 (16.7)</td></tr><tr><td align="center" valign="middle" >Tumour anatomical location: Posterior wall Dome Anterior wall Urachal Left lateral wall Right Lateral wall</td><td align="center" valign="middle" >n (%) 24 (57.1) 8 (19) 5 (11.9) 2 (4.8) 2 (4.8) 1 (2.4)</td></tr></tbody></table></table-wrap><table-wrap id="1_2"><table><tbody><thead><tr><th align="center" valign="middle" >Pathological subtype: AC (NOS) MAC SRAC</th><th align="center" valign="middle" >n (%) 32 (76.2) 6 (14.3) 4 (9.5)</th></tr></thead><tr><td align="center" valign="middle" >Tumour grade: II III</td><td align="center" valign="middle" >n (%) 33 (78.6) 9 (21.4)</td></tr><tr><td align="center" valign="middle" >Associated bilharziasis: Negative Positive</td><td align="center" valign="middle" >n (%) 27 (64.3) 15 (35.7)</td></tr><tr><td align="center" valign="middle" >Intitial clinical stage*: Stage II Stage III Stage IVA Stage IVB (distant metastasis)</td><td align="center" valign="middle" >n (%) 28 (66.7) 7 (16.7) 1 (2.3) 6 (14.3)</td></tr><tr><td align="center" valign="middle" >Curative radical Surgery (n = 27): RC APE PC</td><td align="center" valign="middle" >n (%) 19 (70.4) 5 (18.5) 3 (11.1)</td></tr><tr><td align="center" valign="middle" >Pathological tumour (pT) stage (n = 27): pT2 pT3a pT3b pT4</td><td align="center" valign="middle" >n (%) 9 (33.3) 5 (18.5) 10 (37.1) 3(11.1)</td></tr><tr><td align="center" valign="middle" >Pathological nodal involvement (n = 27): Negative Positive</td><td align="center" valign="middle" >n (%) 22 (81.5) 5 (18.5)</td></tr></tbody></table></table-wrap></table-wrap-group><p>*according to TNM 8th edition [<xref ref-type="bibr" rid="scirp.90132-ref33">33</xref>] , AC: adenocarcinoma, APE: anterior pelvic exenteration, MAC: mucinous adenocarcinoma, NOS: not-otherwise specified, PC: partial cystectomy, RC: radical cystectomy, SD: standard deviation, SRAC: signet ring adenocarcinoma.</p><p>In respect to chemotherapy employed; adjuvant treatment with 4 cycles of gemcitabine and cisplatin was offered to just one case (3.7%) with pT3bN0M0 (stage IIIA). Palliative chemotherapy was given to 11 (26.2%) patients (recurrent, locally advanced and metastatic) with median number of cycles was 6 (range: 1 - 8), gemcitabine and platinum regimen was employed in all cases except one patient who received flouropyrimidine-based regimen (Capecitabine and Oxaliplatin/XELOX). The objective response rate (ORR) in the ten patients who received platinum (Cisplatin in 5 patients and Carboplatin in the other 5) was 0% as 9 cases (90%) showed disease progression (PD) and one patient (10%) had stable disease (SD) according to response evaluation criteria in solid tumours (RECIST v1.1) [<xref ref-type="bibr" rid="scirp.90132-ref34">34</xref>] , regarding the remaining patient who received XELOX; partial response (PR) was the clinical outcome after 6 cycles. Concerning radiation therapy; one patient (3.7%) with pT2bN0M0 (stage II) received adjuvant radiation whereas, palliative irradiation was employed in 9 patients (21.4%) for control of persistent hematuria, bone metastases, brain metastases and pelvic recurrence in 5, 2, 1 and 1 patients, respectively.</p><p>Survival: At the end of follow up period (median: 13 months, range: 1 - 82), twenty two patients were dead. The median DFS and OS were 17.8 &amp; 20.2 months, respectively. The cumulative DFS and OS at 1, 3 &amp; 5 years were 58.7%, 40.7% &amp; 40.7% and 69%, 35.7% &amp; 26.8%, respectively (<xref ref-type="fig" rid="fig2">Figure 2</xref>(a) &amp; <xref ref-type="fig" rid="fig2">Figure 2</xref>(b)). Patients who had negative lymph nodes pathologically, GII tumours and absence of hydronephrosis on imaging had significantly longer DFS contrasted to those with positive nodes (p = 0.011), GIII tumours (p = 0.001) and hydronephrosis (p = 0.047), respectively (<xref ref-type="table" rid="table2">Table 2</xref>, Figures 3(a)-(c)). Cases presented with hematuria, initial clinical stage II and pathologically negative nodes had significantly longer OS compared to those presented with other main complaints (p = 0.007), stage III &amp; IV disease (p &lt; 0.001) and positive nodes (p = 0.037), respectively (<xref ref-type="table" rid="table3">Table 3</xref>, Figures 4(a)-(c)). Age, sex, residency, type of surgery, pathological subtype, grade, presence of bilharziasis, pattern of tumour growth, tumour size and location did not have significant impact on DFS &amp; OS (<xref ref-type="table" rid="table2">Table 2</xref> &amp; <xref ref-type="table" rid="table3">Table 3</xref>). On multivariate analysis, the independent prognostic factor that affected DFS was tumour grade with cases having GIII showed worse DFS compared to GII (p = 0.006) with HR 7.81 (CI 1.79 - 33.98), whereas the only independent variable affected OS was the clinical stage as patients with stage III &amp; IV showed worse survival than stage II (p = 0.001) with HR 4.67 (CI 1.90 - 11.47).</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Disease-free survival (DFS) in relation to clinicopathologic characteristics</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Characteristic</th><th align="center" valign="middle" >N</th><th align="center" valign="middle" >N of events</th><th align="center" valign="middle" >Cumulative DFS at 12 ms (%)</th><th align="center" valign="middle" >Cumulative DFS at 36 ms (%)</th><th align="center" valign="middle" >Cumulative DFS at 60 ms (%)</th><th align="center" valign="middle" >Median DFS estimate (ms)</th><th align="center" valign="middle" >P-value</th></tr></thead><tr><td align="center" valign="middle" >Whole group</td><td align="center" valign="middle" >27</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >58.7</td><td align="center" valign="middle" >40.7</td><td align="center" valign="middle" >40.7</td><td align="center" valign="middle" >17.83</td><td align="center" valign="middle" >NA</td></tr><tr><td align="center" valign="middle" >Gender:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Male Female</td><td align="center" valign="middle" >18 9</td><td align="center" valign="middle" >7 5</td><td align="center" valign="middle" >63.5 50.8</td><td align="center" valign="middle" >41.7 38.1</td><td align="center" valign="middle" >NR 38.1</td><td align="center" valign="middle" >28.98 17.83</td><td align="center" valign="middle" >0.569</td></tr><tr><td align="center" valign="middle" >Age Categories:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >≤50</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >85.7</td><td align="center" valign="middle" >51.4</td><td align="center" valign="middle" >51.4</td><td align="center" valign="middle" >NR</td><td align="center" valign="middle" >0.327</td></tr><tr><td align="center" valign="middle" >&gt;50</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >46.9</td><td align="center" valign="middle" >31.3</td><td align="center" valign="middle" >NR</td><td align="center" valign="middle" >11.18</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >≤60</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >60.6</td><td align="center" valign="middle" >32.5</td><td align="center" valign="middle" >32.5</td><td align="center" valign="middle" >17.83</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&gt;60</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >55.6</td><td align="center" valign="middle" >55.6</td><td align="center" valign="middle" >NR</td><td align="center" valign="middle" >NR</td><td align="center" valign="middle" >0.659</td></tr><tr><td align="center" valign="middle" >Residence:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Rural Urban</td><td align="center" valign="middle" >19 8</td><td align="center" valign="middle" >7 5</td><td align="center" valign="middle" >52.3 71.4</td><td align="center" valign="middle" >52.3 NR</td><td align="center" valign="middle" >52.3 NR</td><td align="center" valign="middle" >NR 17.83</td><td align="center" valign="middle" >0.727</td></tr><tr><td align="center" valign="middle" >Curative Sx:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >RC + PC APE</td><td align="center" valign="middle" >22 5</td><td align="center" valign="middle" >10 2</td><td align="center" valign="middle" >58.6 60.0</td><td align="center" valign="middle" >34.2 60.0</td><td align="center" valign="middle" >NR 60.0</td><td align="center" valign="middle" >17.83 NA</td><td align="center" valign="middle" >0.509</td></tr><tr><td align="center" valign="middle" >Main complaint:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Hematuria Others</td><td align="center" valign="middle" >25 2</td><td align="center" valign="middle" >11 1</td><td align="center" valign="middle" >61.4 NR</td><td align="center" valign="middle" >42.6 NR</td><td align="center" valign="middle" >42.6 NR</td><td align="center" valign="middle" >28.98 2.37</td><td align="center" valign="middle" >*</td></tr><tr><td align="center" valign="middle" >Tumour Growth:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Fungating Ulcerative</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Tumour Size(cm)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >≤5 &gt;5</td><td align="center" valign="middle" >21 6</td><td align="center" valign="middle" >12 0</td><td align="center" valign="middle" >50.2 100</td><td align="center" valign="middle" >29.3 NR</td><td align="center" valign="middle" >29.3 NR</td><td align="center" valign="middle" >18.0 NR</td><td align="center" valign="middle" >0.054</td></tr><tr><td align="center" valign="middle" >Tumour Location:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Posterior wall Others</td><td align="center" valign="middle" >16 11</td><td align="center" valign="middle" >7 5</td><td align="center" valign="middle" >60.6 56.3</td><td align="center" valign="middle" >41.5 45.0</td><td align="center" valign="middle" >41.5 NR</td><td align="center" valign="middle" >28.98 12.86</td><td align="center" valign="middle" >0.818</td></tr><tr><td align="center" valign="middle" >Clinical stage<sup>#</sup></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >II III &amp; IV</td><td align="center" valign="middle" >24 3</td><td align="center" valign="middle" >10 2</td><td align="center" valign="middle" >63.1 33.3</td><td align="center" valign="middle" >41.3 NR</td><td align="center" valign="middle" >NR NR</td><td align="center" valign="middle" >28.98 10.13</td><td align="center" valign="middle" >*</td></tr><tr><td align="center" valign="middle" >pT:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >pT2 pT3 &amp; 4</td><td align="center" valign="middle" >9 18</td><td align="center" valign="middle" >2 10</td><td align="center" valign="middle" >85.7 46.9</td><td align="center" valign="middle" >57.1 33.5</td><td align="center" valign="middle" >57.1 NR</td><td align="center" valign="middle" >NR 11.18</td><td align="center" valign="middle" >0.126</td></tr><tr><td align="center" valign="middle" >pN:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Negative Positive</td><td align="center" valign="middle" >22 5</td><td align="center" valign="middle" >8 4</td><td align="center" valign="middle" >66.2 25.0</td><td align="center" valign="middle" >50.2 NR</td><td align="center" valign="middle" >50.2 NR</td><td align="center" valign="middle" >NR 2.37</td><td align="center" valign="middle" >0.011</td></tr><tr><td align="center" valign="middle" >Hydronephrosis:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Present Absent</td><td align="center" valign="middle" >13 14</td><td align="center" valign="middle" >8 4</td><td align="center" valign="middle" >36.4 81.8</td><td align="center" valign="middle" >27.3 53.7</td><td align="center" valign="middle" >NR 53.7</td><td align="center" valign="middle" >10.13 NR</td><td align="center" valign="middle" >0.047</td></tr><tr><td align="center" valign="middle" >Pathology:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >AC (NOS) MAC &amp; SRAC</td><td align="center" valign="middle" >21 6</td><td align="center" valign="middle" >9 3</td><td align="center" valign="middle" >64.6 40.0</td><td align="center" valign="middle" >41.3 40.0</td><td align="center" valign="middle" >NR 40.0</td><td align="center" valign="middle" >28.98 10.13</td><td align="center" valign="middle" >0.720</td></tr><tr><td align="center" valign="middle" >Tumour grade:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >II III</td><td align="center" valign="middle" >21 6</td><td align="center" valign="middle" >7 5</td><td align="center" valign="middle" >76.5 NR</td><td align="center" valign="middle" >53.1 NR</td><td align="center" valign="middle" >53.1 NR</td><td align="center" valign="middle" >NR 7.04</td><td align="center" valign="middle" >0.001</td></tr><tr><td align="center" valign="middle" >Bilharziasis:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Yes No</td><td align="center" valign="middle" >13 14</td><td align="center" valign="middle" >6 6</td><td align="center" valign="middle" >36.0 75.0</td><td align="center" valign="middle" >36 43.8</td><td align="center" valign="middle" >36 NR</td><td align="center" valign="middle" >10.13 28.98</td><td align="center" valign="middle" >0.272</td></tr></tbody></table></table-wrap><p>#according to TNM 8th edition [<xref ref-type="bibr" rid="scirp.90132-ref33">33</xref>] , *p value not applicaple, AC: adenocarcinoma, APE: anterior pelvic exenteration, MAC: mucinous adenocarcinoma, ms: month, n: number, NA: not applicable, NOS: not-otherwise specified, PC: partial cystectomy, pN: pathological nodal status, pT: pathological tumor stage, RC: radical cystectomy, SRAC: signet ring adenocarcinoma, Sx: surgery.</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Overall survival (OS) in relation to clinicopathologic characteristics</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Characteristic</th><th align="center" valign="middle" >N</th><th align="center" valign="middle" >N of events</th><th align="center" valign="middle" >Cumulative OS at 12 ms (%)</th><th align="center" valign="middle" >Cumulative OS at 36 ms (%)</th><th align="center" valign="middle" >Cumulative OS at 60 ms (%)</th><th align="center" valign="middle" >Median OS estimate (ms)</th><th align="center" valign="middle" >P-value</th></tr></thead><tr><td align="center" valign="middle" >Whole cohort:</td><td align="center" valign="middle" >42</td><td align="center" valign="middle" >22</td><td align="center" valign="middle" >69.4</td><td align="center" valign="middle" >35.7</td><td align="center" valign="middle" >26.8</td><td align="center" valign="middle" >20.23</td><td align="center" valign="middle" >NA</td></tr><tr><td align="center" valign="middle" >Gender:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Male Female</td><td align="center" valign="middle" >27 15</td><td align="center" valign="middle" >13 9</td><td align="center" valign="middle" >74.1 61.5</td><td align="center" valign="middle" >39.1 30.8</td><td align="center" valign="middle" >NR 30.8</td><td align="center" valign="middle" >26.84 12.86</td><td align="center" valign="middle" >0.454</td></tr><tr><td align="center" valign="middle" >Age categories:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >≤50 &gt;50 ≤60 &gt;60</td><td align="center" valign="middle" >10 32 24 18</td><td align="center" valign="middle" >3 19 13 9</td><td align="center" valign="middle" >100 60.2 69.5 88.1</td><td align="center" valign="middle" >51.4 28.2 31.3 44.1</td><td align="center" valign="middle" >51.4 NR 20.9 NR</td><td align="center" valign="middle" >NR 13.29 20.23 26.84</td><td align="center" valign="middle" >0.085 0.657</td></tr><tr><td align="center" valign="middle" >Residence:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Rural Urban</td><td align="center" valign="middle" >29 13</td><td align="center" valign="middle" >14 8</td><td align="center" valign="middle" >67.7 72.7</td><td align="center" valign="middle" >33.2 36.4</td><td align="center" valign="middle" >33.2 NR</td><td align="center" valign="middle" >20.23 15.36</td><td align="center" valign="middle" >0.662</td></tr><tr><td align="center" valign="middle" >Main complaint:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Hematuria Others</td><td align="center" valign="middle" >37 5</td><td align="center" valign="middle" >18 4</td><td align="center" valign="middle" >74.8 26.7</td><td align="center" valign="middle" >40.4 NR</td><td align="center" valign="middle" >30.3 NR</td><td align="center" valign="middle" >26.84 5.16</td><td align="center" valign="middle" >0.007</td></tr><tr><td align="center" valign="middle" >Tumor growth:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Fungating Ulcerative</td><td align="center" valign="middle" >35 7</td><td align="center" valign="middle" >21 1</td><td align="center" valign="middle" >70.9 80</td><td align="center" valign="middle" >29.1 80</td><td align="center" valign="middle" >19.4 NR</td><td align="center" valign="middle" >16.48 NR</td><td align="center" valign="middle" >0.108</td></tr><tr><td align="center" valign="middle" >Tumor Size (cm)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >≤5 &gt;5</td><td align="center" valign="middle" >24 18</td><td align="center" valign="middle" >14 8</td><td align="center" valign="middle" >67.3 72.4</td><td align="center" valign="middle" >36.2 24.8</td><td align="center" valign="middle" >24.2 NR</td><td align="center" valign="middle" >16.48 20.23</td><td align="center" valign="middle" >0.694</td></tr><tr><td align="center" valign="middle" >Tumor location:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Posterior wall Other sites</td><td align="center" valign="middle" >25 17</td><td align="center" valign="middle" >12 10</td><td align="center" valign="middle" >70.4 66.7</td><td align="center" valign="middle" >51.2 16.7</td><td align="center" valign="middle" >34.1 NR</td><td align="center" valign="middle" >44.80 13.58</td><td align="center" valign="middle" >0.296</td></tr><tr><td align="center" valign="middle" >Tumor grade:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >II III</td><td align="center" valign="middle" >33 9</td><td align="center" valign="middle" >16 6</td><td align="center" valign="middle" >67.7 75.0</td><td align="center" valign="middle" >41.0 NR</td><td align="center" valign="middle" >30.7 NR</td><td align="center" valign="middle" >26.84 12.86</td><td align="center" valign="middle" >0.279</td></tr><tr><td align="center" valign="middle" >Hydronephrosis:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Present Absent</td><td align="center" valign="middle" >22 20</td><td align="center" valign="middle" >15 7</td><td align="center" valign="middle" >58.8 81.9</td><td align="center" valign="middle" >17.8 60.6</td><td align="center" valign="middle" >NR 30.3</td><td align="center" valign="middle" >13.29 44.80</td><td align="center" valign="middle" >0.065</td></tr><tr><td align="center" valign="middle" >Pathology:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >AC (NOS) MAC &amp; SRAC</td><td align="center" valign="middle" >32 10</td><td align="center" valign="middle" >16 6</td><td align="center" valign="middle" >70.4 66.7</td><td align="center" valign="middle" >38.0 33.3</td><td align="center" valign="middle" >NR 33.3</td><td align="center" valign="middle" >20.29 13.28</td><td align="center" valign="middle" >0.600</td></tr><tr><td align="center" valign="middle" >Bilharziasis:</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Present Absent</td><td align="center" valign="middle" >15 27</td><td align="center" valign="middle" >8 14</td><td align="center" valign="middle" >59.1 74.7</td><td align="center" valign="middle" >26.3 43.2</td><td align="center" valign="middle" >26.3 NR</td><td align="center" valign="middle" >12.73 20.23</td><td align="center" valign="middle" >0.623</td></tr><tr><td align="center" valign="middle" >Clinical stage<sup>#</sup></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Stage II Stage III &amp; IV</td><td align="center" valign="middle" >28 14</td><td align="center" valign="middle" >10 12</td><td align="center" valign="middle" >82.5 46.2</td><td align="center" valign="middle" >52.0 7.7</td><td align="center" valign="middle" >39.0 NR</td><td align="center" valign="middle" >44.80 7.93</td><td align="center" valign="middle" >&lt;0.001</td></tr><tr><td align="center" valign="middle" >Curative Sx (n = 27):</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >RC + PC APE</td><td align="center" valign="middle" >22 5</td><td align="center" valign="middle" >9 2</td><td align="center" valign="middle" >82.4 80</td><td align="center" valign="middle" >44.6 60</td><td align="center" valign="middle" >NR 60</td><td align="center" valign="middle" >32.24 NR</td><td align="center" valign="middle" >0.735</td></tr><tr><td align="center" valign="middle" >pT (n = 27):</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >pT2 pT3 &amp; 4</td><td align="center" valign="middle" >9 18</td><td align="center" valign="middle" >2 9</td><td align="center" valign="middle" >100 73.3</td><td align="center" valign="middle" >75 38.1</td><td align="center" valign="middle" >NR NR</td><td align="center" valign="middle" >44.8 20.3</td><td align="center" valign="middle" >0.116</td></tr><tr><td align="center" valign="middle" >pN (n = 27):</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></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" >Negative Positive</td><td align="center" valign="middle" >22 5</td><td align="center" valign="middle" >8 3</td><td align="center" valign="middle" >88.9 50.0</td><td align="center" valign="middle" >55.9 NR</td><td align="center" valign="middle" >41.9 NR</td><td align="center" valign="middle" >44.80 6.84</td><td align="center" valign="middle" >0.037</td></tr></tbody></table></table-wrap><p>#according to TNM 8th edition [<xref ref-type="bibr" rid="scirp.90132-ref33">33</xref>] , AC: adenocarcinoma, APE: anterior pelvic exenteration, MAC: mucinous adenocarcinoma, n: number, NA: not applicable, NOS: not-otherwise specified, NR: not reached, PC: partial cystectomy, pN: pathological nodes, pT: pathological tumor stage, RC: radical cystectomy, SRAC: signet ring adenocarcinoma, Sx: surgery.</p></sec><sec id="s6"><title>6. Discussion</title><p>In the current retrospective series of 42 cases of primary bladder AC, the mean age was 55.5 years which is almost identical to Korkes et al. (55.8) [<xref ref-type="bibr" rid="scirp.90132-ref35">35</xref>] , relatively close to Grignon et al. (58.3) [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] and Zaghloul et al. (50.4) [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] and almost 10 years older than in El-Mekresh et al. (46.3) [<xref ref-type="bibr" rid="scirp.90132-ref9">9</xref>] , the latter finding could be referred to the discrepancy of the number of patients and the study duration. There was a male predominance (64%) with M:F ratio 1.8:1, concurring with previous reports from Egypt [<xref ref-type="bibr" rid="scirp.90132-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] and also western reports [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref36">36</xref>] , whereas all the patients (100%) were males in [<xref ref-type="bibr" rid="scirp.90132-ref35">35</xref>] . This sex predilection could be interpreted by that males might be exposed to the hazard factors for developing bladder AC more than females e.g. to bilharziasis in endemic areas through farming work or to chronic irritation by infection and other risk factors in other areas.</p><p>The worldwide incidence of primary bladder AC reported in literature is 0.5% - 2% of all BC [<xref ref-type="bibr" rid="scirp.90132-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] , however, the incidence is higher in areas known with bilharziasis endemicity, ranging from 5% - 11.4% [<xref ref-type="bibr" rid="scirp.90132-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref37">37</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref38">38</xref>] as documented by old series from Egypt e.g. El-Bolkainy et al. reported an incidence of 8.1% in a series of 229 BC cases developed on top of bilharziasis over the period (1967-1970) [<xref ref-type="bibr" rid="scirp.90132-ref39">39</xref>] , also El-Mekresh et al. found an incidence of 9.9% as they demonstrated 185 cases (82% had bilharziasis) of primary AC out of 1870 BC patients post RC over a 25-year period (1970-1995) [<xref ref-type="bibr" rid="scirp.90132-ref9">9</xref>] , these reports could be an evidence confirming that bilharziasis is one of the well documented predisposing factors for the development of bladder AC through inducing metaplastic changes of potentially unsteady urothelium as described in [<xref ref-type="bibr" rid="scirp.90132-ref40">40</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref41">41</xref>] , however, the incidence of bladder AC showed progressive decline in subsequent published Egyptian series e.g. it was 5.2% in the work of Zaghloul et al. as they described 192 bladder AC out of 3659 patients who underwent cystectomy over a ten-year period (1994-2003) [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] , it was 3.8% of all BC cases presented to NCI-E (which is the largest tertiary cancer centre in Egypt) over a twelve- year period (2000-2011) [<xref ref-type="bibr" rid="scirp.90132-ref7">7</xref>] , in the present retrospective series, we depicted 42 cases of primary bladder AC out of a total of 3144 BC cases presented to NCI-E during the studied five-year period (2010-14) representing an incidence of 1.3% which corresponds to the range of the reported global incidence, this downward trend might be strongly explained by the continuing decline in bilharzial infection in Egypt during the last three decades compared to the era of 1970s and 1980s owing to mass governmental struggling and the wide spread availability of anti-bilharzial treatment in the primary health care facilities distributed all over the rural areas of Egypt. In contrast; the old series coming from the States reported an incidence of bladder AC that in congruence with the worldwide incidence; 1.6% during the period (1973-77) in the work of Young et al. [<xref ref-type="bibr" rid="scirp.90132-ref42">42</xref>] , Grignon et al. described only 72 cases through a so long 40-year period (1948-1987) [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] , this discrepancy in incidence between old Egyptian and western series mostly due to the high prevalence of infection with shistosoma haematobium in rural Egypt compared to the west.</p><p>In the present study, the 1 &amp; 5-year OS were 69% &amp; 26.8%, respectively, which corresponds to the previously reported ranges; 23.1% - 87.5% &amp; 5% - 33%, respectively described in [<xref ref-type="bibr" rid="scirp.90132-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref29">29</xref>] , whereas the current 5-year DFS rate was 40.7% close to 46% in [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] while it was 55% in [<xref ref-type="bibr" rid="scirp.90132-ref9">9</xref>] . As regard the relation of different prognostic elements to survival parameters; hematuria which was the chief presenting complaint by the highest percent of patients in the present study (88%), that is similar to previous reports in [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref43">43</xref>] , our outcome showed that those patients had significantly longer OS contrasted to the cases presented with other main complaints (p = 0.007), the authors could owe this finding to the fact that gross hematuria is a pressing caution sign that makes patients seeking medical counselling urgently with consequent diagnosis of the tumour at an early stage. Patients presented with preoperative hydronephrosis in the current series exhibited significantly shorter DFS compared to others without (p = 0.047), a finding which exactly concurring with the work of Bartsch et al. [<xref ref-type="bibr" rid="scirp.90132-ref44">44</xref>] and Lin et al. [<xref ref-type="bibr" rid="scirp.90132-ref45">45</xref>] as hydronephrosis was significantly related to higher T stages in their works which included patients with only urothelial carcinoma contrasting to our study of bladder AC only. High grade (III) tumours demonstrated significantly shorter DFS (p = 0.001), similar results found in [<xref ref-type="bibr" rid="scirp.90132-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] , moreover, it was an independent prognostic factor predicting worse DFS on multivariate analysis.</p><p>Clinical stage at presentation demonstrated a significant effect on OS in the current study; moreover, it was an independent prognostic factor for OS on multivariate analysis, comparable outcomes were reported in [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] . Up to 33% of bladder AC patients have nodal involvement at the moment of presentation [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref18">18</xref>] , in the current study; positive lymph node metastasis was found in 18.5% of the resected patients which is coinciding with El-Bolkainy et al. (19%) [<xref ref-type="bibr" rid="scirp.90132-ref39">39</xref>] , those patients experienced significantly shorter DFS &amp; OS compared to node negative cases (p = 0.011 &amp; 0.037, respectively) similar to the reports of [<xref ref-type="bibr" rid="scirp.90132-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] .</p><p>Fungating/exophytic growth pattern was the most widely recognized finding on initial cystoscopy in 83.3% of the patients in the current series, with posterior wall being the most frequent location of the bladder tumours in 57%, typically as reported by [<xref ref-type="bibr" rid="scirp.90132-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref46">46</xref>] and also similar to [<xref ref-type="bibr" rid="scirp.90132-ref39">39</xref>] when they described features of BC developed on bilharziasis in Egypt. AC-NOS was the pervasive histological subtype in the series in hand (76.2%), these results are in congruence with those of [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] , though the MAC histology was the overwhelming type in [<xref ref-type="bibr" rid="scirp.90132-ref9">9</xref>] . We couldn’t delineate significant effect of AC subtypes on the DFS &amp; OS in consistence with [<xref ref-type="bibr" rid="scirp.90132-ref5">5</xref>] and in contradiction to [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] who reported that the SRAC subtype had significantly worst 5-year DFS compared to other histological subtypes (p = 0.00001), the latter result is concurring with the work of Holmang et al. who reported that SRAC is frequently diagnosed in advanced stage and has a bleak survival rate [<xref ref-type="bibr" rid="scirp.90132-ref47">47</xref>] . The authors might explain this opposing finding by the relatively small number of the whole cohort in the current study compared to [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] (42 vs. 192, respectively) and also the small numbers in the subgroups.</p><p>The role of adjuvant radiation for bladder AC was previously raised in a retrospective study from Egypt where post operative radiotherapy enhanced the 5-year DFS and the local control rates compared to cystectomy alone (p = 0.002 &amp; 0.00001, respectively) specially in locally advanced disease (pT3, pT4a) [<xref ref-type="bibr" rid="scirp.90132-ref17">17</xref>] , however, in the present study; despite 55.6% and 17% of the patients had pT3 and pT4, respectively; radiotherapy was mostly used for palliative intent with adjuvant radiotherapy employed in just a single patient (3.7%) who had pT2b, N0 stage, subsequently we couldn’t derive any conclusions about the impact of adjuvant radiation on the outcome. The authors refer this to the existing absence of level 1 evidence supporting the use of adjuvant radiation in this rare BC subtype and also to the prevailed belief between oncologists that this subtype is mostly radioresistant as reported in other studies [<xref ref-type="bibr" rid="scirp.90132-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.90132-ref23">23</xref>] .</p><p>The role of chemotherapy described for this rare type of BC in the neoadjuvant, adjuvant or metastatic setting still represents an area of great debate and needs continuing intense research. In the current series, we depicted ORR 0% for the 10 (23.8%) patients with recurrent, advanced or metastatic disease who received gemcitabine/platinum regimen used for treating TCC whereas it was 100% for the single patient who received XELOX regimen as for treating adenocarcinoma of primary colorectal origin. These findings reflect the aforementioned lack of consensus between medical oncologist regarding the optimal type of chemotherapy for this tumour and that most of oncologist opt to use conventional protocols employed in combating the most frequent type of bladder cancer (TCC) rather than to be pathology-directed. Similar findings were reported by Siefker-Radtke et al. who retrospectively analysed 42 cases of urachal carcinoma at M.D. Anderson Cancer Centre during a 17-year period (1985-2001), they found ORR 33% in patients with metastatic disease who received palliative chemotherapy containing 5-fluorouracil, so they concluded that regimens used for primary colonic AC might be more advantageous for this tumour than conventional regimens given for TCC, consequently; they stated that the GFLP [gemcitabine, 5-fluorouracil, leucovorin and cisplatin] is their preferred initial protocol for metastatic urachal AC [<xref ref-type="bibr" rid="scirp.90132-ref26">26</xref>] . Another study supporting these data done by Yanagihara et al. who retrospectively evaluated five patients with metastatic urachal cancer received mFOLFOX6 regimen, the ORR was 40% and concluded that this protocol appears to be successful for the management of patients with metastatic urachal cancer [<xref ref-type="bibr" rid="scirp.90132-ref48">48</xref>] , also in consistence with the latter conclusion; Fan &amp; Yang reported long lasting response to mFOLFOX6 and capecitabine for a patient with metastatic primary bladder nonurachal AC [<xref ref-type="bibr" rid="scirp.90132-ref49">49</xref>] .</p></sec><sec id="s7"><title>7. Conclusion</title><p>The authors admit the limitations of retrospective studies, but retrospectivity is the most appropriate way for studying such a rare type of bladder cancer (0.5% - 2%). A notable continuing decrease of the incidence of bladder AC in Egypt is mostly due to the dramatic decrease in bilharzial infection, the incidence in this series (1.3%) is within the worldwide range. The reported 5-year DFS &amp; OS in the current work are in congruence with previous Egyptian and western series. The tumour grade and the clinical stage at presentation were independent prognostic factors for DFS &amp; OS, respectively. Radical surgery is the optimal treatment for locoregional disease but still no consensus about the role of adjuvant radiotherapy or chemotherapy. Antineoplastic protocols used for adenocarcinoma of colorectal cancer seem to be profitable in advanced and metastatic cases. Further larger scale studies are needed to define other risk factors, molecular characterises and optimal management of this unique type of bladder cancer.</p></sec><sec id="s8"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s9"><title>Cite this paper</title><p>Ismail, Y., Kamal, A., Yousof, O., Tahoun, N. and Allam, R. (2019) Primary Bladder Adenocarcinoma: A Five-Year Retrospective Clinicopathologic Study of 42 Cases in Egyptian NCI (2010-14). Journal of Cancer Therapy, 10, 97-116. https://doi.org/10.4236/jct.2018.101008</p></sec></body><back><ref-list><title>References</title><ref id="scirp.90132-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Ferlay, J., Soerjomataram, I., Dikshit, R., Eser, S., Mathers, C., Parkin, D.M., et al. (2015) Cancer Incidence and Mortality Worldwide: Sources, Methods and Major Patterns in GLOBOCAN 2012. 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