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<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">OR</journal-id>
<journal-title-group>
<journal-title>Oncology Reports</journal-title></journal-title-group>
<issn pub-type="ppub">1021-335X</issn>
<issn pub-type="epub">1791-2431</issn>
<publisher>
<publisher-name>D.A. Spandidos</publisher-name></publisher></journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3892/or.2012.1950</article-id>
<article-id pub-id-type="publisher-id">or-28-04-1243</article-id>
<article-categories>
<subj-group>
<subject>Articles</subject></subj-group></article-categories>
<title-group>
<article-title>Microwave-induced thermoablation with Amica-probe is a safe and reproducible method to treat solid renal masses: Results from a phase I study</article-title></title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>BARTOLETTI</surname><given-names>RICCARDO</given-names></name><xref rid="af1-or-28-04-1243" ref-type="aff">1</xref></contrib>
<contrib contrib-type="author">
<name><surname>MELIANI</surname><given-names>ENRICO</given-names></name><xref rid="af1-or-28-04-1243" ref-type="aff">1</xref></contrib>
<contrib contrib-type="author">
<name><surname>SIMONATO</surname><given-names>ALCHIEDE</given-names></name><xref rid="af2-or-28-04-1243" ref-type="aff">2</xref></contrib>
<contrib contrib-type="author">
<name><surname>GONTERO</surname><given-names>PAOLO</given-names></name><xref rid="af3-or-28-04-1243" ref-type="aff">3</xref></contrib>
<contrib contrib-type="author">
<name><surname>BERTA</surname><given-names>GIOVANNA</given-names></name><xref rid="af3-or-28-04-1243" ref-type="aff">3</xref></contrib>
<contrib contrib-type="author">
<name><surname>PALMA</surname><given-names>PAOLO DALLA</given-names></name><xref rid="af4-or-28-04-1243" ref-type="aff">4</xref></contrib>
<contrib contrib-type="author">
<name><surname>LEONARDI</surname><given-names>ELENA</given-names></name><xref rid="af4-or-28-04-1243" ref-type="aff">4</xref></contrib>
<contrib contrib-type="author">
<name><surname>CAI</surname><given-names>TOMMASO</given-names></name><xref rid="af5-or-28-04-1243" ref-type="aff">5</xref><xref ref-type="corresp" rid="c1-or-28-04-1243"/></contrib>
<contrib contrib-type="author">
<name><surname>CARMIGNANI</surname><given-names>GIORGIO</given-names></name><xref rid="af2-or-28-04-1243" ref-type="aff">2</xref></contrib></contrib-group>
<aff id="af1-or-28-04-1243">
<label>1</label>Department of Urology, Santa Maria Annunziata Hospital, University of Florence, Florence</aff>
<aff id="af2-or-28-04-1243">
<label>2</label>Department of Urology, University of Genoa, Genoa</aff>
<aff id="af3-or-28-04-1243">
<label>3</label>Department of Urology, University of Turin, Turin</aff>
<aff id="af4-or-28-04-1243">
<label>4</label>Department of Pathology, Santa Chiara Hospital, Trento, Italy</aff>
<aff id="af5-or-28-04-1243">
<label>5</label>Department of Urology, Santa Chiara Hospital, Trento, Italy</aff>
<author-notes>
<corresp id="c1-or-28-04-1243"><italic>Correspondence to:</italic> Dr Tommaso Cai, Department of Urology, Santa Chiara Hospital, Largo Medaglie d&#x02019;Oro 9, Trento, Italy, E-mail: <email>ktommy@libero.it</email></corresp></author-notes>
<pub-date pub-type="ppub">
<month>10</month>
<year>2012</year></pub-date>
<pub-date pub-type="epub">
<day>06</day>
<month>08</month>
<year>2012</year></pub-date>
<volume>28</volume>
<issue>4</issue>
<fpage>1243</fpage>
<lpage>1248</lpage>
<history>
<date date-type="received">
<day>27</day>
<month>04</month>
<year>2012</year></date>
<date date-type="accepted">
<day>08</day>
<month>06</month>
<year>2012</year></date></history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2012, Spandidos Publications</copyright-statement>
<copyright-year>2012</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/3.0">
<license-p>This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.</license-p></license></permissions>
<abstract>
<p>Microwave thermal ablation (MWTA) could be considered in the future for treating small solid renal masses. The aim of the present study was to determine both the tolerability of the new Amica-probe applicator-induced MWTA used <italic>in vivo</italic> on patients with solid renal masses and the effects of heating on renal tumors and normal renal parenchyma. Fourteen patients with renal masses eligible for open radical nephrectomy were enrolled in this phase I study. All patients underwent MWTA of renal masses during the open surgery procedure before clamping of renal vascular pedicle. The effects of MWTA on patients&#x02019; coagulation and tumor/renal vasculature were investigated. The histological effects of MWTA on the tumor and intralesional vital tumor cell skipping were also evaluated. The MWTA-induced lesion diameters were measured to calculate both the overall ablation volume and the lesion sphericity index (SI). The Clavien-Dindo classification was used. In all patients the RENAL score was 9.4 (<xref rid="b8-or-28-04-1243" ref-type="bibr">8</xref>&#x02013;<xref rid="b12-or-28-04-1243" ref-type="bibr">12</xref>) and the Charlson comorbidity index was 4.8 (<xref rid="b3-or-28-04-1243" ref-type="bibr">3</xref>&#x02013;<xref rid="b7-or-28-04-1243" ref-type="bibr">7</xref>). MWTA-induced lesion size was 44.14 mm (&#x000B1;22.59). Mean SI was 1.08 (&#x000B1;0.2). No significant differences among coagulation clinical parameters were found. No local bleeding after MWTA treatment was reported. According to the Clavien-Dindo classification, there were two grade II perioperative complications due to the tumor extent but not related with the MWTA treatment. No residual vital tumor cells inside the MWTA-induced lesions were found. Telephone interview at 27.4 (&#x000B1;4.2) months mean follow-up did not find any long-term adverse events due to previous MWTA treatment. Amica-Probe applicator-induced MWTA is a safe and reproducible method to treat solid renal masses.</p></abstract>
<kwd-group>
<kwd>microwave</kwd>
<kwd>minimally invasive treatment</kwd>
<kwd>kidney neoplasms</kwd>
<kwd>thermoablation</kwd></kwd-group></article-meta></front>
<body>
<sec sec-type="intro">
<title>Introduction</title>
<p>Prevalence of small solid renal masses in adult population recently increased probably due to the large number of people that daily undergo preventive diagnostic investigations such as ultrasonography and computed tomography (CT) scan for unrelated symptoms, resulting in incidental tumor detection (<xref rid="b1-or-28-04-1243" ref-type="bibr">1</xref>). Patients&#x02019; comorbidities, such as cardiovascular or respiratory diseases, could represent limiting factors for planning adequate subsequent surgical approaches although conservative laparoscopy surgery is now considered the gold standard treatment, particularly for tumors &lt;3&#x02013;4 cm (<xref rid="b2-or-28-04-1243" ref-type="bibr">2</xref>). Minimally invasive procedures, such as cryoablation (CryA) and radiofrequency ablation (RFA), have been recently proposed by different authors as alternative methods of treatment to conservative surgery with satisfactory results in terms of perioperative complications such as hemorrhage episodes or metabolic problems related to prolonged period of general anaesthesia (<xref rid="b3-or-28-04-1243" ref-type="bibr">3</xref>). Some doubts remain on the efficacy of these methods on tumor complete eradication due to the high prevalence of tumor local recurrences due to persistent vital tumor cells in the context of the ablated tissue (tumor skipping) (<xref rid="b4-or-28-04-1243" ref-type="bibr">4</xref>). Both CryA and RFA are based on the application of physical means (cold and heat respectively) at the centre of the lesion to induce tumor tissue necrosis. Both of them are suitable for clinical application either through laparoscopic trocars or ultrasound/CT-guided percutaneous approaches (<xref rid="b5-or-28-04-1243" ref-type="bibr">5</xref>). Microwaves are a source of electromagnetic energy which, similarly to radiofrequency or cryoablation, could be considered in the future for treating small solid renal masses percutaneously or laparoscopically (<xref rid="b5-or-28-04-1243" ref-type="bibr">5</xref>). Indeed, with respect to RFA and CryA, microwave thermal ablation (MWTA) allows for a more rapid and homogeneous ablation, due to its reduced sensitivity to local variations of tissue physical properties (<xref rid="b6-or-28-04-1243" ref-type="bibr">6</xref>,<xref rid="b7-or-28-04-1243" ref-type="bibr">7</xref>). We previously studied the <italic>in vivo</italic> effects of MWTA on porcine kidney, proving that MWTA is a safe and effective procedure. In particular, we demonstrated the absence of viable cells inside the ablation volume and the absence of any damage to the renal parenchyma outside it (<xref rid="b8-or-28-04-1243" ref-type="bibr">8</xref>). Although empirical studies on the effects of MWTA in the treatment of small renal masses were previously reported by other authors on small series of patients, none of them reported adequate information on patients tolerability and pathological effects on ablated tissues (<xref rid="b4-or-28-04-1243" ref-type="bibr">4</xref>,<xref rid="b5-or-28-04-1243" ref-type="bibr">5</xref>). The aim of this phase I prospective multicentre study was to determine both the tolerability of the new Amica-probe V4 applicator-induced MWTA administered <italic>in vivo</italic> on patients with solid renal masses and the effects of heating on the renal tumors and normal renal parenchyma.</p></sec>
<sec sec-type="methods">
<title>Materials and methods</title>
<sec>
<title>Study design</title>
<p>From February 2009 to June 2010, 14 consecutive patients affected by solid renal masses eligible for open radical surgical treatment were enrolled in three different Italian Urological Centers. We considered for enrolling only patients with renal masses who were candidates to open radical nephrectomy in order to obtain useful adjunctive information on both the anatomical extent and the distribution of MWTA on tumor and peritumoral healthy renal tissues. The patients underwent standard laboratory examinations and radiological evaluations before the treatment. The effects of MWTA on patients&#x02019; coagulation, tumor/renal parenchyma and tumor skipping were assessed. Patients were informed on the risk of a new therapy with no long-term follow-up data and agreed to participate in the study. The present study was approved by the Research Ethics Committee in each of the Centers participating in the study (IRB Coordinator Center no. URO/01/2008-322/2008). Written informed consent was obtained from all patients before treatment. The study was conducted in line with Good Clinical Practice guidelines and with the Ethical Principles laid down in the latest version of the Declaration of Helsinki.</p></sec>
<sec>
<title>Inclusion and exclusion criteria</title>
<p>Requirements for inclusion were the presence of a single, solid, contrast-enhanced parenchymal renal mass (attenuation increase, &gt;15 H on contrast-enhanced CT or &gt;15&#x00025; on gadolinium-enhanced MRI) consistent with renal cell carcinoma on preoperative imaging and to be scheduled for radical nephrectomy through an open approach (<xref rid="b9-or-28-04-1243" ref-type="bibr">9</xref>). Patients affected by major concomitant diseases that precluded the surgical treatment, ASA score &#x02264;3, poor performance status (ECOG, 3&#x02013;4), previous abdominal major surgery, severe medical or psychiatric illness that precluded adequate informed consent, &lt;18 or &gt;85 years, who had undergone radiation therapy to the retroperitoneum were excluded.</p></sec>
<sec>
<title>RENAL score and Charlson comorbidity index</title>
<p>The RENAL nephrometry score was calculated in accordance with Kutikov and Uzzo (<xref rid="b10-or-28-04-1243" ref-type="bibr">10</xref>). In brief, standardized points (1&#x02013;3 points/descriptor) were assigned based on tumor size, endophytic/exophytic properties, nearness to collecting system and lesion location relative to polar lines. Moreover, the Charlson comorbidity index was calculated by using the software purposed in the website of the Institute for Algorithmic Medicine (Texas non-profit Corporation) (<ext-link xlink:href="http://www.medal.org/OnlineCalculators/ch1/ch1.13/ch1.13.01.php" ext-link-type="uri">http://www.medal.org/OnlineCalculators/ch1/ch1.13/ch1.13.01.php</ext-link>) (<xref rid="b11-or-28-04-1243" ref-type="bibr">11</xref>).</p></sec>
<sec>
<title>Microwave probe applicator</title>
<p>The system used for MWTA was HS AMICA, with the Amica-probe V4 applicator (Hospital Services SpA, Aprilia, Italy), which is a technical development of a previously described applicator (Amica-probe V3) (<xref rid="b12-or-28-04-1243" ref-type="bibr">12</xref>). Amica-probe V4 includes a coaxial antenna and an integrated hydraulic circuit to cool the coaxial feeding line. The antenna is provided with a patented device (minichoke) for the entrapment of back-propagating waves and is terminated by a sharp point for easy penetration into the tissues (<xref rid="f1-or-28-04-1243" ref-type="fig">Fig. 1</xref>). Control over the coagulative lesion size is obtained by setting the microwave power level and delivery time.</p></sec>
<sec>
<title>Surgical treatment and MWTA</title>
<p>After the surgical exposure of the kidney and before vascular renal pedicle clamping, a Tru-cut biopsy specimen was taken from the tumor, in order to obtain a tumor sample for histopathological analysis. Then, the Amica-probe V4 applicator was inserted in the bed of Tru-cut needle into the tumor. The applicator was placed at least 3 cm deep into the tumor, for tumor size &gt;4&#x02013;5 cm (calculated on the basis of CT scan resolution), and at least 1 cm beyond the tumor, in the case of tumor size &lt;4 cm. Such different applicator insertion methods were used in order to verify the complete tumor ablation in subjects with tumor size &lt;4 cm. For each patient, 50 W microwave power was delivered into the renal tissue for 5 min. The selection of power and time of exposure to MWTA was determined on the basis of previous studies on porcine kidney where these two parameters were standardized to obtain spheroidal shaped repeteable lesions (<xref rid="b8-or-28-04-1243" ref-type="bibr">8</xref>). The probe was removed, the renal blood vessels were promptly legated and the surgeon proceeded to classic radical nephrectomy. The surgical specimen, consisting of the kidney and tumor within the Gerota fascia, was removed en bloc and underwent pathological analysis for standard hystopathological diagnosis, microwave thermo-induced effects in the context of both tumor and healthy renal tissue and tumor skipping evaluation.</p></sec>
<sec>
<title>Heating-induced lesion measurement and histopathological analysis</title>
<p>Pathological samples were collected from the ablated tissues immediately after surgery to investigate neoplastic vital cell skipping. Small tumor samples were collected from the tumor bed after adequate sagittal and horizontal line kidney sections useful for both the tumor and the microwave thermo-induced lesion measurements. These small samples were immediately sectioned and stained with trypan blue according to the procedure described by Allison and Ridolpho (<xref rid="b13-or-28-04-1243" ref-type="bibr">13</xref>), in order to test cell viability. Pathologist thus provided for tumor and lesion measurements and tissues were stored in formalin for subsequent staining with haematoxylin and eosin (H&amp;E) and microscopical analysis. Pathological evaluation was carried out by one dedicated pathologist in each center, in accordance with Bartoletti <italic>et al</italic> (<xref rid="b8-or-28-04-1243" ref-type="bibr">8</xref>). All samples were analyzed to evaluate the effect of microwave energy delivered to renal tissue (no skipping) and the effect of energy on the collecting system or peritumoral healthy renal tissue, as previously described (<xref rid="b8-or-28-04-1243" ref-type="bibr">8</xref>). All ablation lesions were assessed using callipers for both the short-axis diameter (r1, perpendicular to the applicator) and the long-axis diameter (r2, along the applicator). In addition, both diameters were used to calculate the sphericity of the ablation. Sphericity index (SI) was defined as the volume of ablation divided by the volume sphere, using only the greatest diameter. According to Hines-Peralta <italic>et al</italic> (<xref rid="b14-or-28-04-1243" ref-type="bibr">14</xref>), the volume of ablation was defined as the calculated volume of an ellipsoid, obtained by using r1 and r2 radii. As suggested by these authors, SI was simplified to r1<sup>2</sup>/r2 (2); a perfect sphere has an index of 1.0 and an ellipsoid &lt;1.0 (<xref rid="b14-or-28-04-1243" ref-type="bibr">14</xref>).</p></sec>
<sec>
<title>Trypan blue exclusion test</title>
<p>Trypan blue exclusion test (Life Technologies) is able to accurately determine cell viability. In fact, if cells take-up trypan blue, they are considered non-viable. Live cells or tissues with intact cell membranes are not colored. After the Amica-probe application, a sample of the renal lesion was collected and immediately sent to laboratory in isotonic salt solution under refrigerate conditions. Renal cells were added to a solution 0.4&#x00025; of trypan blue in buffered isotonic salt solution, pH 7.2&#x02013;7.3, such as phosphate-buffered saline and were examined immediately under a microscope at low magnification. In order to obtain reproducible results, the sample collection and tissue processing was performed according to Wu <italic>et al</italic> (<xref rid="b15-or-28-04-1243" ref-type="bibr">15</xref>).</p></sec>
<sec>
<title>Preoperative complication evaluation</title>
<p>The classification of perioperative complications was performed using the Clavien-Dindo classification (<xref rid="b16-or-28-04-1243" ref-type="bibr">16</xref>).</p></sec>
<sec>
<title>Statistical analysis</title>
<p>All ablation diameters are reported as the mean (&#x000B1;SD) and were compared using ANOVA, followed by Bonferroni test, when appropriate, with P&lt;0.05 (two-sided) considered to indicate significance. All statistical calculations were performed with the Statistical Package for Social Sciences 11.0 (SPSS, Inc., Chicago, IL, USA).</p>
<p>For the ablation equipment, materials, support was provided by Hospital Services SpA, and the results were analyzed and discussed independently of any influence of the Sponsor Company.</p></sec></sec>
<sec sec-type="results">
<title>Results</title>
<p>Fourteen patients (12 men and 2 women; mean age, 70.9&#x000B1;9.8; range, 53&#x02013;88 years) underwent open radical nephrectomy. The mean age-adjusted Charlson comorbidity index was 4.8 (range, 3&#x02013;7). The mean RENAL score was 9.4 (range, 8&#x02013;12). <xref rid="tI-or-28-04-1243" ref-type="table">Table I</xref> shows the clinical and laboratory characteristics of enrolled patients.</p>
<sec>
<title>Clinical and laboratory results</title>
<p>No significant differences between D-dimer, aPPT and INR values were found before and after MWTA and surgery treatment independently from previous anti-platelet medical treatments. Two patients (14.2&#x00025;) with tumor extension to vena cava (pT3b), showed low grade complications (Clavien II) that required blood transfusions. This procedure was, however, independent from the parenchyma MWTA treatment. All patients had a normal postoperative time of hospitalization (mean, 3.1 days; range, 3&#x02013;5) without relevant complications concerning both the wound healing and the laboratory analyses regularization. No short-term significant bleeding was collected from draining tubes which were removed just before patient discharge. No adverse events due to co-morbidities were observed during hospitalization or after long-term follow-up (27.4&#x000B1;4.2 months). Noticeable absence or reduction bleeding from the tumor was described by different surgeons overall in patients with smaller tumors, although this parameter could not be scientifically quantifiable.</p></sec>
<sec>
<title>Histopathological results</title>
<sec>
<title>Macroscopic evaluation</title>
<p>MW-induced lesion size was 44.14 mm (&#x000B1;22.59). All removed kidneys were sectioned along three different planes (sagittal, orizontal and transversal) in order to obtain precise measurement of both tumor and MWTA-induced lesion diameters. Mean SI of MWTA-induced lesions was 1.08 (&#x000B1;0.2). <xref rid="f2-or-28-04-1243" ref-type="fig">Fig. 2</xref> shows the distribution of SI values among all patients. All pathological and laboratory findings are presented in <xref rid="tII-or-28-04-1243" ref-type="table">Table II</xref>. The inner area of the MWTA-induced lesions appeared pale and necrotic, the middle area hyperemic, while a purple border represented the outer layer. H&amp;E staining showed homogeneous coagulative necrosis at the lesion core (inner area) surrounded by renal cells (<xref rid="f3-or-28-04-1243" ref-type="fig">Fig. 3A</xref>).</p></sec>
<sec>
<title>Microscopic evaluation</title>
<p>Renal cells appear with irreversible cell death, as shown by pyknotic nuclei and nuclear disruption. There were variable amounts of granulation tissue, with immature fibroblasts and inflammatory cells in the boundary region (middle and outer areas). Beyond these, only healthy tissue was found and no skipping was noted in any sample (<xref rid="f3-or-28-04-1243" ref-type="fig">Fig. 3B</xref>). Moreover, histological review of the wide ablation zones showed the inner zone to have uniform cell death by trypan blue exclusion test. No residual vital tumor cells inside the MW-induced lesions were found.</p></sec></sec></sec>
<sec sec-type="discussion">
<title>Discussion</title>
<p>The effects of MWTA on kidney tissue have been recently evaluated and discussed by several authors with conflicting results. Clark <italic>et al</italic> (<xref rid="b9-or-28-04-1243" ref-type="bibr">9</xref>) demonstrated the feasibility of MWTA in 10 patients with large kidney tumors before radical nephrectomy and demonstrated complete tumor cell kill inside the ablated lesions. Liang <italic>et al</italic> (<xref rid="b17-or-28-04-1243" ref-type="bibr">17</xref>) confirmed the efficacy of MWTA on renal tumors by treating 12 patients with small lesions (&lt;4 cm in diameter) and no evidence of recurrence after 20 months of follow-up, while Castle <italic>et al</italic> (<xref rid="b18-or-28-04-1243" ref-type="bibr">18</xref>) reported poor oncologic outcomes and significant complication rates in a series of 10 patients with tumor diameter size ranging from 2.0 to 5.5 cm treated by laparoscopic- or CT-guided percutaneous MWTA. Rational explanations for such similar discrepancies could be easily found by evaluating either the absence of a standardized and reproducible method for microwave administration or the adequate selection of patients. Our previous study on porcine kidney (<xref rid="b8-or-28-04-1243" ref-type="bibr">8</xref>) demonstrated that a standardized method of microwave administration could be obtained by using pre-determined independent variables such as power of treatment and time of exposure to energy. The Amica-probe antenna is a new refrigerated probe able to determine approximately spherical lesions with a maximum of 2.7&#x000B1;0.3 cm in the animal kidney tissue by an exposure time of 5 min and 50 W power (<xref rid="b8-or-28-04-1243" ref-type="bibr">8</xref>). The best results could be obtained by using 15 min of time exposure and 50 W power with induced-lesion SI ~1.0 and diameters from 4.1 to 4.2 cm (&#x000B1;0.1). Moreover, the thermocouple sensors placed ~4 cm radially far from the Amica-probe antenna point of insertion showed temperature peaks of 41&#x000B0;C, thus, confirming the safety of this method on healthy renal tissues. These results could explain the importance of patient selection (only patients with small renal masses could be treated) and reliable technology (this refrigerated probe is able to induce a satisfactory SI) to obtain reproducible methods of treatment and evaluable results. This is the first study describing the use of Amica-probe V4 microwave applicator on human kidney tumors, which has been successfully tested. Although a subjective variability of MWs induced lesion diameters due to both the applicator insertion depth and the tumor water content, tumors until 2 cm could be safely treated by using 50 W power energy and 5 min of exposure time to MWs. Clinical studies on MWTA of small renal masses and conservative surgery should be then conducted to obtain extensive clinical clarifications and indications on this fascinating technique. Microwaves create a thermal field that is absorbed by surrounding tissues proportionally to the tissue water content (<xref rid="b19-or-28-04-1243" ref-type="bibr">19</xref>). Thus, tissues with greater water content absorb more energy and produce heat, while tissues with lower water content produce less heat and propagate microwaves (<xref rid="b20-or-28-04-1243" ref-type="bibr">20</xref>). Testing the Amica-probe antenna on both healthy renal tissue and renal tumor tissue, we found no substantial differences of diffusion of MWs by measuring macroscopically MWTA-induced lesion diameters, although no significant variations of SI were found. This could be related to both the cellular type or the presence of necrosis in the context of the tumor. Nevertheless, large tumors usually present necrotic areas in their context while small tumors tends to be more compact and homogeneous except oncocytomas. All patients selected for this study presented large or complicated renal masses (mean RENAL score, 9.4). This kind of selection aimed to obtain an accurate evaluation of MWs diffusion and spread inside the tumor tissue, thus, avoiding the risk of significant variations in heat-induced lesion diameters due to different tissue resistance of tumor pseudo-capsule. Nevertheless, this could justify future studies on MWTA application on small solid renal masses. The potential tropism of MWs to tumor and renal vasculature represented one of the most important parameters investigated in this study. No differences were found in monitoring the patients haemo-coagulative set up before surgery and after short- and long-term follow-up, showing a limited diffusion of MWs through renal tissue independently from the renal pedicle clamping during the MWTA treatment. All patients underwent open radical nephrectomy after MWTA treatment and only 2/14 of them presented intraoperative bleeding with the need of blood-transfusions due to the presence of a tumor thrombus in the vena cava (Clavien II). The incidence of patients requiring blood-transfusions during radical nephrectomy have been reported as ranging from 18 to 44&#x00025; in relation to tumor extension and the need of extensive surgery (<xref rid="b21-or-28-04-1243" ref-type="bibr">21</xref>). This complication found in our series has not to be considered as relevant and it was not related to the MWTA tumor treatment. No evidence of tumor-cell skipping was found by using vital staining analyisis in all cases. This could demonstrate that local recurrence of disease, previously described by other authors, is probably due to the incomplete ablation of large tumors where the estimation of surgical results have been entrusted to the macroscopically apparent evidence of ablation in case of both laparoscopic- and CT-guided MWs application. The empirical experience of Muto <italic>et al</italic> (<xref rid="b22-or-28-04-1243" ref-type="bibr">22</xref>) confirmed our results demonstrating that MWs application to small renal tumors (1.3&#x02013;4.2 cm) provides good results in terms of tumor follow-up and has to be considered as optimal method for haemostasis making laparoscopic tumor enucleation easier and possible without renal pedicle clamping and haemostatic sutures subsequent to tumor removal. However, the present study shows few limitations that should be taken into account during interpretation of the findings. The MWs diffusion and spread through tumor tissue may vary in relation to its liquid content (water and/or necrosis), thus, large tumors could not be considered as the optimal model although our findings demonstrated satisfactory homogeneous results in terms of both heat-induced lesion diameters and SI.</p>
<p>In conclusion, the Amica-probe V4 microwave antenna is able to determine reproducible results in the treatment of small kidney solid tumors. MWTA is a safe method and could be relatively easily employed for future clinical efficacy and comparative studies.</p></sec></body>
<back>
<ack>
<title>Acknowledgements</title>
<p>We are grateful to all members of the R&amp;D Unit of HS Hospital Service SpA (Aprilia, Italy) for their technical assistance and to Professor John Denton for manuscript language revision.</p></ack>
<ref-list>
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<floats-group>
<fig id="f1-or-28-04-1243" position="float">
<label>Figure 1</label>
<caption>
<p>Sagittal section of Amica-probe V4.</p></caption>
<graphic xlink:href="OR-28-04-1243-g00.gif"/></fig>
<fig id="f2-or-28-04-1243" position="float">
<label>Figure 2</label>
<caption>
<p>Distribution of sphericity index values among all treated patients.</p></caption>
<graphic xlink:href="OR-28-04-1243-g01.gif"/></fig>
<fig id="f3-or-28-04-1243" position="float">
<label>Figure 3</label>
<caption>
<p>Pathological findings after micro-wave-thermal-ablation (H&amp;E; magnification, &#x000D7;40). (A) Gross inspection of the ablated kidney tissue. (B) Three areas of ablation were noted when compared to the peripheral normal-looking parenchyma (NT). The inner area appeared pale and necrotic (N), the middle area hyperemic (HYP), while the outer layer is represented by a purple border (PB).</p></caption>
<graphic xlink:href="OR-28-04-1243-g02.gif"/></fig>
<table-wrap id="tI-or-28-04-1243" position="float">
<label>Table I</label>
<caption>
<p>Patient characteristics at baseline.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="bottom">Characteristics</th>
<th align="center" valign="bottom">Mean</th>
<th align="center" valign="bottom">SD</th>
<th align="center" valign="bottom">Median</th>
<th align="center" valign="bottom">Range</th></tr></thead>
<tbody>
<tr>
<td align="left" valign="top">Age (years)</td>
<td align="center" valign="top">70.9</td>
<td align="center" valign="top">9.8</td>
<td align="center" valign="top">70</td>
<td align="center" valign="top">53&#x02013;88</td></tr>
<tr>
<td align="left" valign="top">Charlson CI</td>
<td align="center" valign="top">4.8</td>
<td align="center" valign="top">1.2</td>
<td align="center" valign="top">4</td>
<td align="center" valign="top">4&#x02013;7</td></tr>
<tr>
<td align="left" valign="top">Lesion diameter (mm)</td>
<td align="center" valign="top">47.00</td>
<td align="center" valign="top">18.7</td>
<td align="center" valign="top">44</td>
<td align="center" valign="top">40&#x02013;92</td></tr>
<tr>
<td align="left" valign="top">RENAL score</td>
<td align="center" valign="top">9.4</td>
<td align="center" valign="top">1.1</td>
<td align="center" valign="top">9</td>
<td align="center" valign="top">8&#x02013;12</td></tr>
<tr>
<td align="left" valign="top">D-dimer (mg/l)</td>
<td align="center" valign="top">226.8</td>
<td align="center" valign="top">87</td>
<td align="center" valign="top">225.5</td>
<td align="center" valign="top">102.5&#x02013;433.3</td></tr>
<tr>
<td align="left" valign="top">INR</td>
<td align="center" valign="top">1.01</td>
<td align="center" valign="top">0.08</td>
<td align="center" valign="top">0.95</td>
<td align="center" valign="top">0.89&#x02013;1.11</td></tr>
<tr>
<td align="left" valign="top">aPTT</td>
<td align="center" valign="top">31</td>
<td align="center" valign="top">3.9</td>
<td align="center" valign="top">30.5</td>
<td align="center" valign="top">23&#x02013;37.5</td></tr></tbody></table>
<table-wrap-foot><fn id="tfn1-or-28-04-1243">
<p>Enrolled patients, n&#x0003D;14 (12 males, 2 females). SD, standard deviation; Charlson CI, Charlson comorbidity index.</p></fn></table-wrap-foot></table-wrap>
<table-wrap id="tII-or-28-04-1243" position="float">
<label>Table II</label>
<caption>
<p>Pathological and laboratory findings after treatment.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th colspan="3" align="left" valign="bottom">Pathological findings</th></tr></thead>
<tbody>
<tr>
<td colspan="2" align="left" valign="top">Histological findings</td>
<td align="center" valign="top">13 RCC</td></tr>
<tr>
<td colspan="2" align="left" valign="top"/>
<td align="center" valign="top">1 oncocytoma</td></tr>
<tr>
<td colspan="2" align="left" valign="top">Pathological stage</td>
<td align="center" valign="top">2 T1a</td></tr>
<tr>
<td colspan="2" align="left" valign="top"/>
<td align="center" valign="top">5 T1b</td></tr>
<tr>
<td colspan="2" align="left" valign="top"/>
<td align="center" valign="top">1 T2</td></tr>
<tr>
<td colspan="2" align="left" valign="top"/>
<td align="center" valign="top">3 T3a</td></tr>
<tr>
<td colspan="2" align="left" valign="top"/>
<td align="center" valign="top">2 T3b</td></tr>
<tr>
<td colspan="2" align="left" valign="top">Fuhrman grade</td>
<td align="center" valign="top">&#x02212; G1</td></tr>
<tr>
<td colspan="2" align="left" valign="top"/>
<td align="center" valign="top">4 G2</td></tr>
<tr>
<td colspan="2" align="left" valign="top"/>
<td align="center" valign="top">6 G3</td></tr>
<tr>
<td colspan="2" align="left" valign="top"/>
<td align="center" valign="top">3 G4</td></tr>
<tr>
<td colspan="2" align="left" valign="top">Complications (Clavien grade)</td>
<td align="center" valign="top">2, grade II</td></tr>
<tr>
<td colspan="3" align="left" valign="top">
<hr/></td></tr>
<tr>
<td align="left" valign="top">Laboratory findings</td>
<td align="center" valign="top">Mean</td>
<td align="center" valign="top">Difference (P-value)</td></tr>
<tr>
<td colspan="3" align="left" valign="top">
<hr/></td></tr>
<tr>
<td align="left" valign="top">D-dimer pre (mg/l)</td>
<td align="center" valign="top">226.85</td>
<td align="center" valign="top">0.21</td></tr>
<tr>
<td align="left" valign="top">D-dimer post (mg/l)</td>
<td align="center" valign="top">445.69</td>
<td align="center" valign="top"/></tr>
<tr>
<td align="left" valign="top">INR pre</td>
<td align="center" valign="top">1.01</td>
<td align="center" valign="top">0.92</td></tr>
<tr>
<td align="left" valign="top">INR post</td>
<td align="center" valign="top">1.10</td>
<td align="center" valign="top"/></tr>
<tr>
<td align="left" valign="top">aPTT pre</td>
<td align="center" valign="top">31</td>
<td align="center" valign="top">0.34</td></tr>
<tr>
<td align="left" valign="top">aPTT post</td>
<td align="center" valign="top">31.69</td>
<td align="center" valign="top"/></tr></tbody></table>
<table-wrap-foot><fn id="tfn2-or-28-04-1243">
<p>RCC, renal cell carcinoma.</p></fn></table-wrap-foot></table-wrap></floats-group></article>
