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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">MCO</journal-id>
<journal-title-group>
<journal-title>Molecular and Clinical Oncology</journal-title>
</journal-title-group>
<issn pub-type="ppub">2049-9450</issn>
<issn pub-type="epub">2049-9469</issn>
<publisher>
<publisher-name>D.A. Spandidos</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3892/mco.2016.933</article-id>
<article-id pub-id-type="publisher-id">MCO-0-0-933</article-id>
<article-categories>
<subj-group>
<subject>Articles</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Conformal 3D planned radiotherapy for pelvic lymphoceles following surgery for urological cancer: A case study</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author"><name><surname>Janssen</surname><given-names>Stefan</given-names></name>
<xref rid="af1-mco-0-0-933" ref-type="aff">1</xref>
<xref rid="af2-mco-0-0-933" ref-type="aff">2</xref>
<xref rid="c1-mco-0-0-933" ref-type="corresp"/></contrib>
<contrib contrib-type="author"><name><surname>K&#x00E4;smann</surname><given-names>Lukas</given-names></name>
<xref rid="af2-mco-0-0-933" ref-type="aff">2</xref></contrib>
<contrib contrib-type="author"><name><surname>Cegla</surname><given-names>Robert</given-names></name>
<xref rid="af1-mco-0-0-933" ref-type="aff">1</xref></contrib>
<contrib contrib-type="author"><name><surname>Rades</surname><given-names>Dirk</given-names></name>
<xref rid="af2-mco-0-0-933" ref-type="aff">2</xref></contrib>
</contrib-group>
<aff id="af1-mco-0-0-933"><label>1</label>Private Practice of Radiation Oncology, D-30161 Hannover, Germany</aff>
<aff id="af2-mco-0-0-933"><label>2</label>Department of Radiation Oncology, University of L&#x00FC;beck, D-23538 L&#x00FC;beck, Germany</aff>
<author-notes>
<corresp id="c1-mco-0-0-933"><italic>Correspondence to</italic>: Dr Stefan Janssen, Private Practice of Radiation Oncology, 10 Rundestr, D-30161 Hannover, Germany, E-mail: <email>s.janssen@strahlentherapie.de</email></corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>08</month>
<year>2016</year></pub-date>
<pub-date pub-type="epub">
<day>14</day>
<month>06</month>
<year>2016</year></pub-date>
<volume>5</volume>
<issue>2</issue>
<fpage>342</fpage>
<lpage>344</lpage>
<history>
<date date-type="received"><day>10</day><month>03</month><year>2015</year></date>
<date date-type="accepted"><day>25</day><month>05</month><year>2016</year></date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2016, Spandidos Publications</copyright-statement>
<copyright-year>2016</copyright-year>
</permissions>
<abstract>
<p>The aim of the present study was to evaluate the outcome and toxicity of 3D conformal radiotherapy (RT) for persistent lymphoceles following surgery for urological cancer. A total of 6 patients with bladder (n=1) and prostate cancer (n=5), with persistent lymphoceles following surgery for a primary tumor were treated with total doses of 10&#x2013;12 Gy (1 Gy single dose) after computed tomography (CT) based 3D planning in order to suspend secretion. No acute or chronic toxicities were observed. In 5 patients, secretion of lymph fluid resolved after RT and in 1 patient RT had no effect. After a mean follow-up of 21 months (range, 5&#x2013;47 months), no patient suffered from any symptoms concerning his former lymphoceles. This is the first analysis, to the best of our knowledge, to evaluate a homogenous patient collective of urological cancer patients with persistent lymphoceles after surgery for the initial tumor. RT to lymphoceles in urological cancer patient is effective, very well-tolerated and should be offered to patients with persistent secretion following drainage.</p>
</abstract>
<kwd-group>
<kwd>radiotherapy</kwd>
<kwd>urological cancer</kwd>
<kwd>postoperative lymphoceles</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec sec-type="intro">
<title>Introduction</title>
<p>Lymphoceles are an abnormal collection of lymphatic fluid occurring following surgery. They can cause abdominal pain, deep vein thrombosis or lower urinary tract problems (<xref rid="b1-mco-0-0-933" ref-type="bibr">1</xref>). Incidence, for example following open radical prostatectomy with pelvic lymph node dissection, varies in the literature between 3 and 14&#x0025; (<xref rid="b2-mco-0-0-933" ref-type="bibr">2</xref>). While treatment options encompass percutaneous aspiration with or without instillation of sclerosing agents and laparoscopic marsupialization, no standard is defined (<xref rid="b1-mco-0-0-933" ref-type="bibr">1</xref>,<xref rid="b3-mco-0-0-933" ref-type="bibr">3</xref>). Very few papers have focussed on radiotherapy (RT) as an alternative treatment option using different doses and techniques (<xref rid="b4-mco-0-0-933" ref-type="bibr">4</xref>&#x2013;<xref rid="b7-mco-0-0-933" ref-type="bibr">7</xref>). The aim of the present analysis was to evaluate outcome and toxicity of a homogenous treatment schedule and modern technique for patients with postoperative persistent lymphoceles in the setting of malignant urological disease.</p>
</sec>
<sec>
<title>Case study</title>
<p>Following radical prostatectomy/cystectomy with lymphadenectomy, 6 patients developed a pelvic lymphocele, which persisted after percutaneous drainage. Each patient (seven treatment volumes in total) was treated with external beam RT using 3D planned treatment with virtual simulation after planning CT. Clinical target volume (CTV) was contoured, including the entire lymphocele with a margin of 1&#x2013;2 cm, creating the planning target volume (PTV). Photons of 6 and 18MV energy were selected and 3&#x2013;5 coplanar fields were used (<xref rid="f1-mco-0-0-933" ref-type="fig">Fig. 1</xref>). Of the patients, 1 patient was simultaneously irradiated to the prostate bed (66 Gy; 2 Gy single dose). Patient and treatment-associated parameters are summarized in <xref rid="tI-mco-0-0-933" ref-type="table">Table I</xref>.</p>
<p>No acute toxicities or chronic side effects were observed. Of the 6 patients, 5 patients exhibited secretion of lymph fluid, which was resolved after RT (<xref rid="tI-mco-0-0-933" ref-type="table">Table I</xref>). In 4 patients, secretion was already reduced during RT, while 1 patient responded time-delayed without further therapy (8 weeks after RT) (<xref rid="tI-mco-0-0-933" ref-type="table">Table I</xref>). In 1 patient, RT caused no effect, making a marsupialization necessary. Following a mean follow-up of 21 months (range, 5&#x2013;47 months), no patient suffered from any symptoms concerning his former lymphoceles. All drainages could be removed.</p>
</sec>
<sec sec-type="discussion">
<title>Discussion</title>
<p>Persistent lymphoceles are a common problem following pelvic surgery, particularly when lymphadenectomy is performed (<xref rid="b3-mco-0-0-933" ref-type="bibr">3</xref>). Different approaches exist for the treatment of persistent lymphoceles but no standard is defined.</p>
<p>In previous literature, there are four studies exclusively focusing on RT for persistent lymphoceles (<xref rid="b4-mco-0-0-933" ref-type="bibr">4</xref>&#x2013;<xref rid="b6-mco-0-0-933" ref-type="bibr">6</xref>,<xref rid="b8-mco-0-0-933" ref-type="bibr">8</xref>). From 1989&#x2013;1998, Neu <italic>et al</italic> (<xref rid="b4-mco-0-0-933" ref-type="bibr">4</xref>) treated 29 patients after vascular surgery with a single daily dose of 1 Gy up to 3&#x2013;12 Gy. The majority of patients were treated with electrons (7&#x2013;18 MeV) (<xref rid="b4-mco-0-0-933" ref-type="bibr">4</xref>). Also, following vascular surgery, Dietl <italic>et al</italic> (<xref rid="b6-mco-0-0-933" ref-type="bibr">6</xref>) treated 28 patients for inguinal lymphorrhea with single doses of 2&#x2013;3 Gy up to 8&#x2013;15 Gy. An orthovoltage of 120&#x2013;300 KV energy was used (<xref rid="b6-mco-0-0-933" ref-type="bibr">6</xref>). The study group of Mayer <italic>et al</italic> (<xref rid="b5-mco-0-0-933" ref-type="bibr">5</xref>) treated patients with fistulas after different, mostly vascular surgeries in different localizations with orthovoltage or electrons in majority. The single doses ranged from 0.3&#x2013;2.0 Gy with total doses of 1&#x2013;12 Gy (<xref rid="b5-mco-0-0-933" ref-type="bibr">5</xref>). Previously, Jereczek-Fossa <italic>et al</italic> (<xref rid="b8-mco-0-0-933" ref-type="bibr">8</xref>) showed RT after prostatectomy in the presence of asymptomatic lymphoceles to be feasible for integrating the lymphocele into the treatment plan of the prostate fossa with maximum doses to the lymphoceles of 5.7&#x2013;73.3 Gy (<xref rid="b8-mco-0-0-933" ref-type="bibr">8</xref>). Taken together, patient collectives of the above mentioned retrospective studies are heterogenous in localization, treatment technique, single and total doses, and primary surgery.</p>
<p>In the present study patients with urological cancer, primarily prostate cancer, were treated for inguinal/iliacal lymphoceles with a homogenous treatment schedule. Contrasting to the other study groups, a more precise RT technique was applied. Prior to the initiation of the treatment, a planning CT was performed, on which the planning target volume (lymphocele) was contoured. Afterwards a 3D treatment plan was generated. This allowed a more precise and conformal dose coverage of the target volume and sparing of the organs at risk compared with clinical approaches. In line with this, no acute or late side effects were observed.</p>
<p>The response rates (suspended secretion or removal of drains) varied between 76 and 93&#x0025; in the literature, and compare well with the present findings (83&#x0025;).</p>
<p>A limitation of the present retrospective case series is without any doubt the small number of patients. Nevertheless, in the absence of prospective studies, the present case series is the first, to the best of our knowledge, to show the effectiveness and safety of modern RT to persistent lymphoceles in patients with urological cancer.</p>
<p>In conclusion, 3D conformal RT for persistent pelvic lymphoceles in patients with urological cancer is effective and very well-tolerated. Urological surgeons must be aware of this treatment option, particularly following the failure of other treatment modalities.</p>
</sec>
</body>
<back>
<ref-list>
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</back>
<floats-group>
<fig id="f1-mco-0-0-933" position="float">
<label>Figure 1.</label>
<caption><p>3D conformal treatment plan for right inguinal lymphocele. Color-wash illustration showing dose distribution.</p></caption>
<graphic xlink:href="mco-05-02-0342-g00.tif"/>
</fig>
<table-wrap id="tI-mco-0-0-933" position="float">
<label>Table I.</label>
<caption><p>Patient and treatment-related factors.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="bottom">Factor</th>
<th align="center" valign="bottom">Patient 1</th>
<th align="center" valign="bottom">Patient 2</th>
<th align="center" valign="bottom">Patient 3</th>
<th align="center" valign="bottom">Patient 4</th>
<th align="center" valign="bottom">Patient 5</th>
<th align="center" valign="bottom">Patient 6</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">Location</td>
<td align="left" valign="top">Left inguinal</td>
<td align="left" valign="top">Left inguinal</td>
<td align="left" valign="top">Left iliacal</td>
<td align="left" valign="top">Left and righ iliacal</td>
<td align="left" valign="top">Right iliacal</td>
<td align="left" valign="top">Left inguinal</td>
</tr>
<tr>
<td align="left" valign="top">Gender</td>
<td align="left" valign="top">Male</td>
<td align="left" valign="top">Male</td>
<td align="left" valign="top">Male</td>
<td align="left" valign="top">Male</td>
<td align="left" valign="top">Male</td>
<td align="left" valign="top">Male</td>
</tr>
<tr>
<td align="left" valign="top">Age at RT</td>
<td align="left" valign="top">61</td>
<td align="left" valign="top">75</td>
<td align="left" valign="top">71</td>
<td align="left" valign="top">79</td>
<td align="left" valign="top">70</td>
<td align="left" valign="top">69</td>
</tr>
<tr>
<td align="left" valign="top">Tumor site</td>
<td align="left" valign="top">Prostate</td>
<td align="left" valign="top">Bladder</td>
<td align="left" valign="top">Prostate</td>
<td align="left" valign="top">Prostate</td>
<td align="left" valign="top">Prostate</td>
<td align="left" valign="top">Prostate</td>
</tr>
<tr>
<td align="left" valign="top">Interval surgery-RT</td>
<td align="left" valign="top">26 days</td>
<td align="left" valign="top">4 months</td>
<td align="left" valign="top">18 days</td>
<td align="left" valign="top">25 days</td>
<td align="left" valign="top">5 months</td>
<td align="left" valign="top">3 months</td>
</tr>
<tr>
<td align="left" valign="top">Previous treatment for lymphocele</td>
<td align="left" valign="top">Percutaneous drainage</td>
<td align="left" valign="top">Percutaneous drainage and slerotic agents</td>
<td align="left" valign="top">Percutaneous drainage and doxicyclin</td>
<td align="left" valign="top">Percutaneous drainage and slerotic agents</td>
<td align="left" valign="top">No previous therapy</td>
<td align="left" valign="top">Percutaneous drainage</td>
</tr>
<tr>
<td align="left" valign="top">Total/single dose</td>
<td align="left" valign="top">12/1 Gy</td>
<td align="left" valign="top">12/1 Gy</td>
<td align="left" valign="top">12/1 Gy</td>
<td align="left" valign="top">10/1 Gy</td>
<td align="left" valign="top">10/1 Gy</td>
<td align="left" valign="top">10/1 Gy</td>
</tr>
<tr>
<td/>
<td/>
<td/>
<td/>
<td/>
<td align="left" valign="top">In addition to RT to prostate bed (66 Gy)</td>
</tr>
<tr>
<td align="left" valign="top">PTV (ml)</td>
<td align="left" valign="top">69 ml</td>
<td align="left" valign="top">172 ml</td>
<td align="left" valign="top">57 ml</td>
<td align="left" valign="top">119 and 88 ml</td>
<td align="left" valign="top">114 ml</td>
<td align="left" valign="top">76 ml</td>
</tr>
<tr>
<td align="left" valign="top">Toxicity</td>
<td align="left" valign="top">None</td>
<td align="left" valign="top">None</td>
<td align="left" valign="top">None</td>
<td align="left" valign="top">None</td>
<td align="left" valign="top">None</td>
<td align="left" valign="top">None</td>
</tr>
<tr>
<td align="left" valign="top">Follow up</td>
<td align="left" valign="top">16 months</td>
<td align="left" valign="top">20 months</td>
<td align="left" valign="top">14 months</td>
<td align="left" valign="top">24 months</td>
<td align="left" valign="top">5 months</td>
<td align="left" valign="top">47 months</td>
</tr>
<tr>
<td align="left" valign="top">Early response</td>
<td align="left" valign="top">150 ml residuum (no initial value), drainage drawn</td>
<td align="left" valign="top">600 to 300 ml</td>
<td align="left" valign="top">1,000 to 300 ml</td>
<td align="left" valign="top">800 to 300 ml</td>
<td align="left" valign="top">150 to 0 ml</td>
<td align="left" valign="top">Persistent (500 ml)</td>
</tr>
<tr>
<td align="left" valign="top">Late response</td>
<td align="left" valign="top">Resolved</td>
<td align="left" valign="top">Resolved</td>
<td align="left" valign="top">Resolved</td>
<td/>
<td align="left" valign="top">Resolved</td>
<td align="left" valign="top">Secondary marsupialization, now no symptoms</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="tfn1-mco-0-0-933"><p>RT, radiotherapy; PTV, planning target volume.</p></fn>
</table-wrap-foot>
</table-wrap>
</floats-group>
</article>
