11 research outputs found

    Results of univariate Kaplan-Meier survival analysis for overall survival.

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    Results of univariate Kaplan-Meier survival analysis for overall survival.</p

    Prognostic Value of SUVmax Measured by Pretreatment Fluorine-18 Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography in Patients with Ewing Sarcoma

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    <div><p>Aim</p><p>The aim of this retrospective study was to determine whether glucose metabolism assessed by using Fluorine-18 (F-18) fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) provides prognostic information independent of established prognostic factors in patients with Ewing sarcoma.</p><p>Methods</p><p>We retrospectively reviewed the medical records of 34 patients (men, 19; women, 15; mean age, 14.5 ± 9.7 years) with pathologically proven Ewing sarcoma. They had undergone F-18 FDG PET/CT as part of a pretreatment workup between September 2006 and April 2012. In this analysis, patients were classified by age, sex, initial location, size, and maximum standardized uptake value (SUVmax). The relationship between FDG uptake and survival was analyzed using the Kaplan-Meier method with the log-rank test and Cox’s proportional hazards regression model.</p><p>Results</p><p>The median survival time for all 34 subjects was 999 days and the median SUV by using PET/CT was 5.8 (range, 2–18.1). Patients with a SUVmax ≤ 5.8 survived significantly longer than those with a SUVmax > 5.8 (median survival time, 1265 vs. 656 days; p = 0.002). Survival was also found to be significantly related to age (p = 0.024), size (p = 0.03), and initial tumor location (p = 0.036). Multivariate analysis revealed that a higher SUVmax (p = 0.003; confidence interval [CI], 3.63–508.26; hazard ratio [HR], 42.98), older age (p = 0.023; CI, 1.34–54.80; HR, 8.59), and higher stage (p = 0.03; CI, 1.21–43.95; HR, 7.3) were associated with worse overall survival.</p><p>Conclusions</p><p>SUVmax measured by pretreatment F-18-FDG PET/CT can predict overall survival in patients with Ewing sarcoma.</p></div

    Kaplan–Meier survival curves depicting overall survival.

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    <p>(A) SUVmax, (B) initial tumor location (b; other locations of the primary tumor were the thigh muscles, arm muscles, lungs, bowel and soft tissues in 5, 2, 2, 1, and 2 patients, respectively), (C) age, and (D) tumor size and (E) stage.</p

    Heteronuclear Gd-<sup>99m</sup>Tc Complex of DTPA-Bis(histidylamide) Conjugate as a Bimodal MR/SPECT Imaging Probe

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    The work describes the synthesis and in vivo application of heterotrimetallic complexes of the type {Gd­(H<sub>2</sub>O)­[(M­(H<sub>2</sub>O)­(CO)<sub>3</sub>)<sub>2</sub>(<b>1</b>)]} {<b>1</b> = DTPA-bis­(histidyl-amide); <i>M</i> = Re (<b>3a</b>); <sup>99m</sup>Tc (<b>3b</b>)} for dual modality MR/SPECT imaging. Here, the DTPA-bis­(histidylamide) conjugate functions as a trinucleating chelate incorporating Gd in the DTPA core with Re or <sup>99m</sup>Tc in the pair of histidylamide side arms. The two complexes are chemically equivalent as revealed by HPLC, and their “cocktail mixture” (<b>3a</b> + <b>3b</b>) has demonstrated itself to be essentially a single bimodal imaging probe. The present system has thus overcome the sensitivity difference problem between MRI and SPECT and paved the way for practical applications

    Gadolinium Complex of <sup>125</sup>I/<sup>127</sup>I‑RGD-DOTA Conjugate as a Tumor-Targeting SPECT/MR Bimodal Imaging Probe

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    The work describes the synthesis and in vivo application of [Gd­(L)­(H<sub>2</sub>O)]·<i>x</i>H<sub>2</sub>O, where L is a (<sup>125</sup>I/<sup>127</sup>I-RGD)- DOTA conjugate, as a tumor-targeting SPECT/MR bimodal imaging probe. Here, (<sup>125</sup>I/<sup>127</sup>I-RGD)-DOTA signifies a “cocktail mixture” of radioisotopic (<b>1a</b>, L = <sup>125</sup>I-RGD-DOTA) and natural (<b>1b</b>, L = <sup>127</sup>I-RGD-DOTA) Gd complexes. The two complexes are chemically equivalent as revealed by HPLC, and their cocktail mixture exhibits the integrin-specific tumor enhancement, demonstrating that they constitute essentially a single bimodal imaging probe. Employment of a cocktail mixture thus proves to be a sole and practical approach to overcome the sensitivity difference problem between MRI and SPECT

    Simple Methods for Tracking Stem Cells with <sup>64</sup>Cu-Labeled DOTA-hexadecyl-benzoate

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    The purpose of this study was to evaluate <sup>64</sup>Cu-labeled hexadecyl-1,4,7,10-tetraazacyclododecane-tetraacetic acid-benzoate (<sup>64</sup>Cu-DOTA-HB) (<b>1</b>) as positron emission tomography (PET) radiotracer for stem cell imaging. Hexadecyl-DOTA-benzoate (DOTA-HB) (<b>2</b>) was efficiently labeled with <sup>64</sup>Cu (>99%), and cell labeling efficiency with adipose-derived stem cells (ADSCs) was over 50%. Labeling with <b>1</b> did not compromise cell viability. In the PET imaging, intramuscularly transplanted <b>1</b>-labeled ADSCs were monitored for 18 h in normal rat heart. These results indicate that <b>1</b> can be utilized as a promising radiotracer for monitoring of transplanted stem cells
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