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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1016/j.brachy.2022.01.006</dc:identifier><dc:language>eng</dc:language><dc:creator>Lozares-Cordero, Sergio</dc:creator><dc:creator>González Pérez, Victor</dc:creator><dc:creator>Pellejero-Pellejero, Santiago</dc:creator><dc:creator>Rodríguez Ruiz, Lucia</dc:creator><dc:creator>Guinot Rodríguez, José Luis</dc:creator><dc:creator>Villafranca-Iturre, Elena</dc:creator><dc:creator>Méndez-Villamón, Agustina</dc:creator><dc:creator>Gandía Martínez, Almudena</dc:creator><dc:creator>Fuentemilla-Urío, Naiara</dc:creator><dc:creator>Ruggeri, Ricardo</dc:creator><dc:title>Feasibility of electronic brachytherapy in cervix cancer–A dosimetric comparison of different brachytherapy techniques</dc:title><dc:identifier>ART-2022-146971</dc:identifier><dc:description>Introducción: This study analyzes cases in which electronic brachytherapy (eBT) led to acceptable treatment plans in cervical cancer. Findings were compared with dosimetry values obtained in 192 Ir-based treatments according to the high-risk clinical target volume (HR-CTV) and the disease stage. 

Material and methods: We retrospectively analyzed 48 patients with cervical cancer from two centers. The patients were treated with 192 Ir based on MRI. It was possible to use interstitial needles via an Utrecht-type applicator. Dosimetry was simulated using eBT and the parameters D90 and D98 (HR-CTV) and D2cc, D1cc, and D0.1cc (bladder, rectum, and sigmoid colon) were evaluated. The Mann-Whitney U test was used for comparison. The overall cohort of patients was analyzed, as were the sub-cohorts based on stage (FIGO stages I + IIA, IIB and III–IV). Finally, the dosimetry of the eBT plans was evaluated, and the plans obtained were classified as “good”, “acceptable”, or “poor”. 

Results: Statistically significant differences were found between the eBT and 192 Ir plans for D98 (HR-CTV), D1cc and D0.1cc (bladder), and D1cc and D0.1cc (sigmoid colon). A total of 31 cases (64.6%) were considered good, seven (14.6%) were considered acceptable, and 10 (20.8%) were considered poor. For volumes &lt; 30 cc, all the plans were good or acceptable; for volumes &gt; 30 cc, 54.3% were good, and 71.4% were good or acceptable. By stage, eBT plans for patients with stage IB–IIA disease were good in 100%, whereas those for patients with stage IIB were good in 70.6% and III–IV disease were good in 50%. 

Conclusions: eBT provides appropriate dosimetry for treatment of cervical cancer in selected cases.</dc:description><dc:date>2022</dc:date><dc:source>http://zaguan.unizar.es/record/165293</dc:source><dc:doi>10.1016/j.brachy.2022.01.006</dc:doi><dc:identifier>http://zaguan.unizar.es/record/165293</dc:identifier><dc:identifier>oai:zaguan.unizar.es:165293</dc:identifier><dc:identifier.citation>Brachytherapy 21, 4 (2022), 389-396</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>https://creativecommons.org/licenses/by/4.0/deed.es</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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