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<article xml:lang="en" article-type="research-article">
<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">OL</journal-id>
<journal-title-group>
<journal-title>Oncology Letters</journal-title></journal-title-group>
<issn pub-type="ppub">1792-1074</issn>
<issn pub-type="epub">1792-1082</issn>
<publisher>
<publisher-name>D.A. Spandidos</publisher-name></publisher></journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3892/ol_00000067</article-id>
<article-id pub-id-type="publisher-id">ol-01-02-0379</article-id>
<article-categories>
<subj-group>
<subject>Articles</subject></subj-group></article-categories>
<title-group>
<article-title><sup>99m</sup>Tc-sestamibi scintigraphy used to evaluate tumor response to neoadjuvant chemotherapy in locally advanced breast cancer: A quantitative analysis</article-title></title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>KOGA</surname><given-names>KATIA HIROMOTO</given-names></name><xref rid="af1-ol-01-02-0379" ref-type="aff">1</xref><xref ref-type="corresp" rid="c1-ol-01-02-0379"/></contrib>
<contrib contrib-type="author">
<name><surname>MORIGUCHI</surname><given-names>SONIA MARTA</given-names></name><xref rid="af5-ol-01-02-0379" ref-type="aff">5</xref></contrib>
<contrib contrib-type="author">
<name><surname>NETO</surname><given-names>JORGE NAH&#x000C1;S</given-names></name><xref rid="af2-ol-01-02-0379" ref-type="aff">2</xref></contrib>
<contrib contrib-type="author">
<name><surname>PERES</surname><given-names>STELA VERZINHASSE</given-names></name><xref rid="af7-ol-01-02-0379" ref-type="aff">7</xref></contrib>
<contrib contrib-type="author">
<name><surname>SILVA</surname><given-names>EDUARDO TIN&#x000D3;IS DA</given-names></name><xref rid="af1-ol-01-02-0379" ref-type="aff">1</xref></contrib>
<contrib contrib-type="author">
<name><surname>SARRI</surname><given-names>ALMIR JOS&#x000C9;</given-names></name><xref rid="af6-ol-01-02-0379" ref-type="aff">6</xref></contrib>
<contrib contrib-type="author">
<name><surname>MICHELIN</surname><given-names>ODAIR CARLITO</given-names></name><xref rid="af3-ol-01-02-0379" ref-type="aff">3</xref></contrib>
<contrib contrib-type="author">
<name><surname>MARQUES</surname><given-names>MARIANGELA ESTHER ALENCAR</given-names></name><xref rid="af4-ol-01-02-0379" ref-type="aff">4</xref></contrib>
<contrib contrib-type="author">
<name><surname>GRIVA</surname><given-names>BEATRIZ LOTUFO</given-names></name><xref rid="af1-ol-01-02-0379" ref-type="aff">1</xref></contrib></contrib-group>
<aff id="af1-ol-01-02-0379">
<label>1</label>Department of Nuclear Medicine, Botucatu Medical School, Sao Paulo State University (UNESP), S&#x000E3;o Paulo</aff>
<aff id="af2-ol-01-02-0379">
<label>2</label>Department of Obstetrics and Gynecology, Botucatu Medical School, Sao Paulo State University (UNESP), S&#x000E3;o Paulo</aff>
<aff id="af3-ol-01-02-0379">
<label>3</label>Department of Medical Clinic, Botucatu Medical School, Sao Paulo State University (UNESP), S&#x000E3;o Paulo</aff>
<aff id="af4-ol-01-02-0379">
<label>4</label>Department of Pathology, Botucatu Medical School, Sao Paulo State University (UNESP), S&#x000E3;o Paulo</aff>
<aff id="af5-ol-01-02-0379">
<label>5</label>Department of Nuclear Medicine, Barretos Cancer Hospital, Barretos, S&#x000E3;o Paulo, Brazil</aff>
<aff id="af6-ol-01-02-0379">
<label>6</label>Department of Physiotherapy, Barretos Cancer Hospital, Barretos, S&#x000E3;o Paulo, Brazil</aff>
<aff id="af7-ol-01-02-0379">
<label>7</label>Center for Researcher Support, Barretos Cancer Hospital, Barretos, S&#x000E3;o Paulo, Brazil</aff>
<author-notes>
<corresp id="c1-ol-01-02-0379"><italic>Correspondence to:</italic> Dr Katia Hiromoto Koga, Department of Nuclear Medicine, Botucatu Medical School, Sao Paulo State University (UNESP), S&#x000E3;o Paulo, Brazil, E-mail: <email>khkoga@bol.com.br</email></corresp></author-notes>
<pub-date pub-type="ppub">
<month>3</month>
<year>2010</year></pub-date>
<pub-date pub-type="epub">
<day>01</day>
<month>3</month>
<year>2010</year></pub-date>
<volume>1</volume>
<issue>2</issue>
<fpage>379</fpage>
<lpage>382</lpage>
<history>
<date date-type="received">
<day>16</day>
<month>9</month>
<year>2009</year></date>
<date date-type="accepted">
<day>30</day>
<month>11</month>
<year>2009</year></date></history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2010, Spandidos Publications</copyright-statement>
<copyright-year>2010</copyright-year></permissions>
<abstract>
<p>To evaluate the tumor response to neoadjuvant chemotherapy, <sup>99m</sup>Tc-sestamibi breast scintigraphy was proposed as a quantitative method. Fifty-five patients with ductal carcinoma were studied. They underwent breast scintigraphy before and after neoadjuvant chemotherapy, along with clinical assessment and surgical specimen analysis. The regions of interest on the lesion and contralateral breast were identified, and the pixel counts were used to evaluate lesion uptake in relation to background radiation. The ratio of these counts before to after neoadjuvant chemotherapy was assessed. The decrease in uptake rate due to chemotherapy characterized the scintigraphy tumor response. The Kruskal-Wallis test was used to compare the mean scintigraphic tumor response and histological type. Dunn&#x02019;s multiple comparison test was used to detect differences between histological types. The Mann-Whitney test was used to compare means between quantitative and qualitative variables: scintigraphic tumor response vs. clinical response and uptake before chemotherapy vs. scintigraphic tumor response. The Spearman&#x02019;s test was used to correlate the quantitative variables of clinical reduction in tumor size and scintigraphic tumor response. All of the variables compared presented significant differences. The change in <sup>99m</sup>Tc-sestamibi uptake noted on breast scintigraphy, before to after neoadjuvant chemotherapy, may be used as an effective method for evaluating the response to neoadjuvant chemotherapy, since this quantification reflects the biological behavior of the tumor towards the chemotherapy regimen. Furthermore, additional analysis on the uptake rate before chemotherapy may accurately predict treatment response.</p></abstract>
<kwd-group>
<kwd>breast cancer</kwd>
<kwd>neoadjuvant chemotherapy</kwd>
<kwd><sup>99m</sup>Tc-sestamibi</kwd>
<kwd>scintigraphy</kwd>
<kwd>quantitative analysis</kwd></kwd-group></article-meta></front>
<body>
<sec sec-type="intro">
<title>Introduction</title>
<p>Breast cancer is the second most common type of cancer worldwide and the most common among women. It accounts for approximately 22&#x00025; of new cancer cases among women each year (<xref rid="b1-ol-01-02-0379" ref-type="bibr">1</xref>), and the 5-year survival rate among the worldwide population is 61&#x00025;. This high mortality rate is related to late diagnosis, with the presence of tumors of large dimensions and lymph node metastases.</p>
<p>Locally advanced breast cancer comprises tumors greater than 5 cm in diameter, with wall or skin invasion, metastases to fixed lymph nodes (<xref rid="b2-ol-01-02-0379" ref-type="bibr">2</xref>,<xref rid="b3-ol-01-02-0379" ref-type="bibr">3</xref>) and inflammatory carcinoma. Treatment for this is multidisciplinary, consisting of preoperative chemotherapy, surgery, radiotherapy and postoperative chemotherapy (<xref rid="b4-ol-01-02-0379" ref-type="bibr">4</xref>&#x02013;<xref rid="b6-ol-01-02-0379" ref-type="bibr">6</xref>).</p>
<p>Preoperative or neoadjuvant chemotherapy is standard treatment for individuals with locally advanced breast cancer (<xref rid="b7-ol-01-02-0379" ref-type="bibr">7</xref>&#x02013;<xref rid="b10-ol-01-02-0379" ref-type="bibr">10</xref>). It has been found to substantially improve the survival of these patients (<xref rid="b6-ol-01-02-0379" ref-type="bibr">6</xref>,<xref rid="b11-ol-01-02-0379" ref-type="bibr">11</xref>,<xref rid="b12-ol-01-02-0379" ref-type="bibr">12</xref>). It provides better local control over the disease, with increased likelihood that the breast surgery will be conservative (<xref rid="b4-ol-01-02-0379" ref-type="bibr">4</xref>,<xref rid="b5-ol-01-02-0379" ref-type="bibr">5</xref>,<xref rid="b13-ol-01-02-0379" ref-type="bibr">13</xref>). Moreover, this type of chemotherapy treats preexisting microscopic systemic disease and enables the evaluation of tumor resistance <italic>in vivo</italic> (<xref rid="b14-ol-01-02-0379" ref-type="bibr">14</xref>).</p>
<p>Reduction in tumor volume has been used as the standard criterion for response evaluation among solid tumors such as breast carcinoma (<xref rid="b15-ol-01-02-0379" ref-type="bibr">15</xref>). Techniques that measure changes in the molecular biology of the tumor, such as Doppler ultrasonography, functional magnetic resonance and nuclear medicine are promising methods for the identification of tumors that present a favorable response, with great accuracy (<xref rid="b16-ol-01-02-0379" ref-type="bibr">16</xref>&#x02013;<xref rid="b18-ol-01-02-0379" ref-type="bibr">18</xref>).</p>
<p>Breast scintigraphy is a well-established diagnostic imaging technique (<xref rid="b19-ol-01-02-0379" ref-type="bibr">19</xref>) of relatively low cost compared with positron emission tomography and magnetic resonance imaging. This technique can also be used as a method for evaluating the response of breast carcinoma to chemotherapy treatment (<xref rid="b20-ol-01-02-0379" ref-type="bibr">20</xref>), thereby providing an <italic>in vivo</italic> indication of the chemosensitivity of the tumor (<xref rid="b8-ol-01-02-0379" ref-type="bibr">8</xref>).</p>
<p>Based on the limitations of the clinical examination as well as the main biological characteristics of <sup>99m</sup>Tc-sestamibi uptake in malignant lesions, an evaluation of the tumor response to neoadjuvant chemotherapy treatment through quantification of <sup>99m</sup>Tc-sestamibi was proposed using scintigrams from individuals with locally advanced breast cancer.</p></sec>
<sec sec-type="methods">
<title>Materials and methods</title>
<p>This was a cross-sectional study conducted between 2000 and 2008. Prior approval had been obtained from the institution&#x02019;s research ethics committee. Fifty-five female patients with a diagnosis of locally advanced ductal invasive breast cancer were included. They underwent neoadjuvant chemotherapy and surgical complementation, with evaluation of the response to treatment through clinical measurements and scintigraphy.</p>
<sec>
<title>Neoadjuvant chemotherapy</title>
<p>The patients underwent chemotherapy consisting of either the AC regimen (doxorubicin hydrochloride, 60 mg/m<sup>2</sup> of body surface and cyclophosphamide, 600 mg/m<sup>2</sup> of body surface) or the FEC regimen (5-fluorouracil, 500 mg/m<sup>2</sup> of body surface; epirubicin, 60 mg/m<sup>2</sup> of body surface and cyclophosphamide, 500 mg/m<sup>2</sup> of body surface).</p></sec>
<sec>
<title>Evaluation of tumor response to neoadjuvant chemotherapy by means of clinical measurements</title>
<p>Tumor measurements were made by a clinical oncologist at two points: before starting and after completing the neoadjuvant chemotherapy. The size in cm was calculated as the mean diameter between the two largest axes. The clinical tumor response was based on the change in tumor size before and after the neoadjuvant chemotherapy, expressed as a percentage. The response was classified into two groups; tumor reduction &gt;60&#x00025; and &lt;60&#x00025;.</p></sec>
<sec>
<title><sup>99m</sup>Tc-sestamibi breast scintigraphy</title>
<p>Breast scintigraphy was performed at two points: before starting and after completing the neoadjuvant chemotherapy, simultaneously with the clinical measurements of the tumor. The images were acquired by a Siemens gamma camera (Orbiter model), coupled to an Icon computer with software version 7.5 and circular detector. A foam pad of 30 cm in thickness was used with openings lateral to the breast projection (<xref rid="b21-ol-01-02-0379" ref-type="bibr">21</xref>,<xref rid="b22-ol-01-02-0379" ref-type="bibr">22</xref>). A low-energy high-resolution collimator was used with a matrix of 128&#x000D7;128 pixels, a photopeak of 140 keV and a window of 15&#x00025;. The image acquisition lasted for 10 min, starting 10 min after injection. Posterior oblique and lateral images with magnification were obtained. The patient was in a prone position with the breasts hanging and the collimator was fitted into the openings. Anterior thoracic and axillary images without magnification were obtained with the patient in a supine position. For all of the examinations <sup>99m</sup>Tc-sestamibi was used, which has a labeling efficiency of &gt;95&#x00025;. It was administered through a vein in the foot or the arm contralateral to the compromised breast.</p>
<p>Quantification of <sup>99m</sup>Tc-sestamibi uptake was carried out on the lateral images of the breasts by creating two identical regions of interest: one on the tumor and the other in the mirror position on the contralateral breast. Pixel counting was performed in these regions. The tumor <sup>99m</sup>Tc-sestamibi uptake rate was determined as the pixel count ratio between the region of interest in the tumor and the mirror region in the contralateral breast. The pretreatment <sup>99m</sup>Tc-sestamibi uptake rate (BUR) and post-treatment <sup>99m</sup>Tc-sestamibi uptake rate (AUR) were obtained from scintigraphic evaluations performed before starting and after completing the neoadjuvant chemotherapy, respectively. The scintigraphic tumor response (STR) was obtained from the following equation: STR &#x0003D; (100 - AUR)/(BUR &#x000D7; 100)&#x00025;.</p></sec>
<sec>
<title>Histological evaluation</title>
<p>The results from the diagnostic biopsy and surgical specimen were analyzed by means of histological sections (4&#x02013;5 &#x003BC;m), cut from paraffin blocks. Hematoxylin and eosin staining was used.</p></sec>
<sec>
<title>Statistical analysis</title>
<p>To calculate the sample size a correlation coefficient (r) of 0.44 was used in the preliminary analysis. Results showed that a minimum of 45 patients would be needed. The descriptive analysis consisted of calculations of absolute and relative frequencies and central trend and dispersion measurements. The Kolmogorov-Smirnov test was used to evaluate the adherence to the normal distribution curve. Since the variables were found not to present a normal distribution, non-parametric tests were used. The Kruskal-Wallis test was used to compare the mean scintigraphic tumor response and histological type. Dunn&#x02019;s multiple comparison test was used to detect differences between histological types. The Mann-Whitney test was used to compare means between quantitative and qualitative variables: scintigraphic tumor response vs. clinical tumor response and pretreatment <sup>99m</sup>Tc-sestamibi uptake vs. scintigraphic tumor response. The Spearman&#x02019;s test was used to correlate the quantitative variables of clinical reduction in tumor size and scintigraphic tumor response. The level of significance was set at p&lt;0.05.</p></sec></sec>
<sec sec-type="results">
<title>Results</title>
<p>The patients evaluated (n&#x0003D;55) were aged between 28 and 68 years (mean 50.5; SD, 9.8; median 51). The number of cycles of chemotherapy ranged from 2 to 8 (mean 3.9; SD, 0.9; median 4). The interval between the scintigraphic examinations before starting and after completing neoadjuvant chemotherapy ranged from 2 to 7 months (mean 3.4; SD, 1.1; median 3).</p>
<p>Residual tumor material was observed in 49 surgical specimens, consisting of invasive ductal carcinoma in 21 cases (38.2&#x00025;) and an association between invasive ductal carcinoma and <italic>in situ</italic> ductal carcinoma in 28 cases (50.9&#x00025;). In six cases (10.9&#x00025;), the tumor response was complete. <xref rid="tI-ol-01-02-0379" ref-type="table">Table I</xref> shows a comparison between the mean scintigraphic tumor response and the different findings from the surgical specimen. The mean scintigraphic tumor response was found to be greatest in tumors that were reduced to zero, followed by those that were purely invasive ductal carcinomas. The mean scintigraphic tumor response was least in tumors in which there was an associated <italic>in situ</italic> component (p&#x0003D;0.011).</p>
<p>The <sup>99m</sup>Tc-sestamibi BUR ranged from 1.18 to 10.13 (mean 3.40&#x000B1;0.22), while the AUR ranged from 0.74 to 3.59 (mean 1.88&#x000B1;0.10). Thus, the overall mean scintigraphic tumor response rate was 38.31&#x000B1;3.26 (&#x00025;). A higher pretreatment <sup>99m</sup>Tc-sestamibi uptake showed greater response rates (<xref rid="tII-ol-01-02-0379" ref-type="table">Table II</xref>).</p>
<p>A positive correlation was noted between the clinical and scintigraphic responses (r&#x0003D;0.44; p&#x0003D;0.001). The scintigraphic response was greater in the tumors with a clinical response &gt;60&#x00025; (p&#x0003D;0.04) (<xref rid="tIII-ol-01-02-0379" ref-type="table">Table III</xref>).</p></sec>
<sec sec-type="discussion">
<title>Discussion</title>
<p>Although clinical examinations are currently standard in evaluating tumor response to chemotherapy treatment, these measurements do not reflect the biological characteristics of tumors, nor do they reflect the real reduction in tumor size. This is because these measurements do not discriminate between inflammatory and healing processes in viable tumors.</p>
<p>On the other hand, the uptake characteristics and efflux dynamics of <sup>99m</sup>Tc-sestamibi have shown a high correlation with the biological behavior of breast tumors, particularly in relation to aggressiveness and chemoresistance.</p>
<p>In the present study, the focus was on the relationship between the <sup>99m</sup>Tc-sestamibi uptake in locally advanced breast tumors and the histological type, and between this uptake and the clinically measured response, as a method for evaluating the response to chemotherapy treatment.</p>
<p>Based on the evaluation of the tumor histology in the surgical specimen, we observed that the individuals with invasive ductal carcinoma presented a greater scintigraphic tumor response than those who had an association with an <italic>in situ</italic> component. This finding may reflect the lower response of <italic>in situ</italic> carcinomas to chemotherapy, thus suggesting that calculation of the <sup>99m</sup>Tc-sestamibi uptake has additional usefulness for possible prediction of the chemotherapy response to different types of carcinomas.</p>
<p>With regard to comparing the pretreatment <sup>99m</sup>Tc-sestamibi uptake with the scintigraphic tumor response, Del Vecchio <italic>et al</italic> (<xref rid="b23-ol-01-02-0379" ref-type="bibr">23</xref>) obtained similar results and stated that high early <sup>99m</sup>Tc-sestamibi uptake in breast carcinomas was related to high rates of cell proliferation. This indicates greater aggressiveness of tumor behavior and correlates directly with a better and faster tumor response to chemotherapy. On the other hand, the tumors with a lower <sup>99m</sup>Tc-sestamibi uptake showed a lower scintigraphic response. This finding may be related, not only to the histological type, but also to the chemoresistance that was indicated by the inverse correlation between the intensity of <sup>99m</sup>Tc-sestamibi uptake and Bcl-2 levels (<xref rid="b24-ol-01-02-0379" ref-type="bibr">24</xref>).</p>
<p>We observed that almost all of our patients presented a reduction in <sup>99m</sup>Tc-sestamibi uptake (n&#x0003D;54) after chemotherapy. Mankoff <italic>et al</italic> (<xref rid="b20-ol-01-02-0379" ref-type="bibr">20</xref>), Marshall <italic>et al</italic> (<xref rid="b25-ol-01-02-0379" ref-type="bibr">25</xref>) and Cwikla <italic>et al</italic> (<xref rid="b26-ol-01-02-0379" ref-type="bibr">26</xref>) also reported a reduction in the tumor-to-background ratio, thus showing that <sup>99m</sup>Tc-sestamibi uptake reflects the metabolic activity of the tumor and its reduction consequent to chemotherapy (<xref rid="b25-ol-01-02-0379" ref-type="bibr">25</xref>). Wilczek <italic>et al</italic> (<xref rid="b27-ol-01-02-0379" ref-type="bibr">27</xref>) found a significant reduction in the tumor-to-background ratio after the conclusion of neoadjuvant chemotherapy, which was confirmed by the tumor regression noted in the histological evaluation of the surgical specimens. These findings suggest that calculating the scintigraphic tumor response should be included as a safe parameter when evaluating tumor regression.</p>
<p>Quantitative analysis of breast scintigraphy using <sup>99m</sup>Tc-sestamibi was shown to be an additional tool for evaluating the preoperative chemotherapy response, given that the variation in <sup>99m</sup>Tc-sestamibi uptake reflects the biological behavior of the tumor. Thus, a quantitative analysis of breast scintigraphy using <sup>99m</sup>Tc-sestamibi should be included in the approach towards assessing tumor response related to preoperative chemotherapy.</p></sec></body>
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<floats-group>
<table-wrap id="tI-ol-01-02-0379" position="float">
<label>Table I</label>
<caption>
<p>Comparison between mean scintigraphic tumor response (STR) in percentages and the histological findings from the surgical specimen.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Specimen</th>
<th align="center" valign="top">No. (&#x00025;)</th>
<th align="center" valign="top">Mean STR&#x00025; (SD)</th>
<th align="center" valign="top">Median</th>
<th align="center" valign="top">Min-Max</th>
<th align="center" valign="top">P-value<xref rid="tfn1-ol-01-02-0379" ref-type="table-fn">a</xref></th></tr></thead>
<tbody>
<tr>
<td align="left" valign="top">Absence of tumor</td>
<td align="right" valign="top">6 (10.9)</td>
<td align="center" valign="top">63.22 (16.83)</td>
<td align="center" valign="top">71.26</td>
<td align="right" valign="top">39.05&#x02013;80.86</td>
<td align="center" valign="top">0.011</td></tr>
<tr>
<td align="left" valign="top">IDC</td>
<td align="right" valign="top">21 (38.2)</td>
<td align="center" valign="top">40.58 (20.26)</td>
<td align="center" valign="top">38.55</td>
<td align="right" valign="top">7.93&#x02013;77.28</td>
<td align="center" valign="top"/></tr>
<tr>
<td align="left" valign="top">IDC&#x0002B;ISDC</td>
<td align="right" valign="top">28 (50.9)</td>
<td align="center" valign="top">31.28 (24.94)</td>
<td align="center" valign="top">19.20</td>
<td align="right" valign="top">&#x02212;0.83&#x02013;75.61</td>
<td align="center" valign="top"/></tr>
<tr>
<td align="left" valign="top">Total</td>
<td align="right" valign="top">55 (100)</td>
<td align="center" valign="top"/>
<td align="center" valign="top"/>
<td align="right" valign="top"/>
<td align="center" valign="top"/></tr></tbody></table>
<table-wrap-foot><fn id="tfn1-ol-01-02-0379">
<label>a</label>
<p>Kruskal-Wallis test.</p></fn><fn id="tfn2-ol-01-02-0379">
<p>IDC, invasive ductal carcinoma; IDC&#x0002B;ISDC, invasive ductal carcinoma &#x0002B; <italic>in situ</italic> ductal carcinoma.</p></fn></table-wrap-foot></table-wrap>
<table-wrap id="tII-ol-01-02-0379" position="float">
<label>Table II</label>
<caption>
<p>Mean <sup>99m</sup>Tc-sestamibi uptake rate before starting neoadjuvant chemotherapy (BUR) compared with scintigraphic tumor response (STR) groups (&gt;60&#x00025; and &lt;60&#x00025;).</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">STR</th>
<th align="center" valign="top">No. (&#x00025;)</th>
<th align="center" valign="top">Mean BUR (SD)</th>
<th align="center" valign="top">Median</th>
<th align="center" valign="top">Min-Max</th>
<th align="center" valign="top">P-value<xref rid="tfn3-ol-01-02-0379" ref-type="table-fn">a</xref></th></tr></thead>
<tbody>
<tr>
<td align="left" valign="top">&lt;60&#x00025;</td>
<td align="center" valign="top">42 (76.4)</td>
<td align="center" valign="top">2.82 (0.96)</td>
<td align="center" valign="top">2.55</td>
<td align="left" valign="top">1.18&#x02013;5.50</td>
<td align="center" valign="top">&lt;0.001</td></tr>
<tr>
<td align="left" valign="top">&gt;60&#x00025;</td>
<td align="center" valign="top">13 (23.6)</td>
<td align="center" valign="top">5.26 (2.03)</td>
<td align="center" valign="top">5.22</td>
<td align="left" valign="top">2.54&#x02013;10.13</td>
<td align="center" valign="top"/></tr>
<tr>
<td align="left" valign="top">Total</td>
<td align="center" valign="top">55 (100)</td>
<td align="center" valign="top"/>
<td align="center" valign="top"/>
<td align="left" valign="top"/>
<td align="center" valign="top"/></tr></tbody></table>
<table-wrap-foot><fn id="tfn3-ol-01-02-0379">
<label>a</label>
<p>Mann-Whitney test.</p></fn></table-wrap-foot></table-wrap>
<table-wrap id="tIII-ol-01-02-0379" position="float">
<label>Table III</label>
<caption>
<p>Mean scintigraphic tumor response (STR) in relation to groups with reduction in clinical measurement &gt; 60&#x00025; and &lt;60&#x00025; (CTR).</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">CTR</th>
<th align="center" valign="top">No. (&#x00025;)</th>
<th align="center" valign="top">Mean STR&#x00025; (SD)</th>
<th align="center" valign="top">Median</th>
<th align="center" valign="top">Min-Max</th>
<th align="center" valign="top">P-value<xref rid="tfn4-ol-01-02-0379" ref-type="table-fn">a</xref></th></tr></thead>
<tbody>
<tr>
<td align="left" valign="top">&lt;60&#x00025;</td>
<td align="left" valign="top">27 (49)</td>
<td align="center" valign="top">31.16 (22.7)</td>
<td align="center" valign="top">23.9</td>
<td align="right" valign="top">&#x02212;0.8&#x02013;75.6</td>
<td align="center" valign="top">0.040</td></tr>
<tr>
<td align="left" valign="top">&gt;60&#x00025;</td>
<td align="left" valign="top">28 (51)</td>
<td align="center" valign="top">45.26 (23.9)</td>
<td align="center" valign="top">48.3</td>
<td align="right" valign="top">1.3&#x02013;80.8</td>
<td align="center" valign="top"/></tr>
<tr>
<td align="left" valign="top">Total</td>
<td align="left" valign="top">55 (100)</td>
<td align="center" valign="top"/>
<td align="center" valign="top"/>
<td align="right" valign="top"/>
<td align="center" valign="top"/></tr></tbody></table>
<table-wrap-foot><fn id="tfn4-ol-01-02-0379">
<label>a</label>
<p>Mann-Whitney test.</p></fn><fn id="tfn5-ol-01-02-0379">
<p>CTR, clinical tumor response.</p></fn></table-wrap-foot></table-wrap></floats-group></article>
