Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/51694
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dc.contributor.authorEkkasit Tharavichitkulen_US
dc.contributor.authorPitchayaponne Klunkinen_US
dc.contributor.authorVicharn Lorvidhayaen_US
dc.contributor.authorVimol Sukthomyaen_US
dc.contributor.authorSomvilai Chakrabhanduen_US
dc.contributor.authorNantaka Pukanhaphanen_US
dc.contributor.authorImjai Chitapanaruxen_US
dc.contributor.authorRazvan Galalaeen_US
dc.date.accessioned2018-09-04T06:06:29Z-
dc.date.available2018-09-04T06:06:29Z-
dc.date.issued2012-03-01en_US
dc.identifier.issn13499157en_US
dc.identifier.issn04493060en_US
dc.identifier.other2-s2.0-84863434668en_US
dc.identifier.other10.1269/jrr.11038en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84863434668&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/51694-
dc.description.abstractEfficacy of different schedules of HDR brachytherapy in concurrent chemoradiotherapy was evaluated. The study compared the effectiveness of the two HDR brachytherapy schedules which have the same Biological Effective Dose (BED) in locally advanced cervical carcinoma that was treated with concurrent chemoradiotherapy. Included in the study were 377 randomly selected patients with advanced carcinoma of the cervix uteri who were treated during the period 2004-2006. Patients were divided into Group I: 7.2 Gy × 3 fractions and Group II: 6 Gy × 4 fractions. With a median follow-up time of 35 months, local control, disease-free survival and overall survival rates were 80.8%, 63.4%, 98.8% in group I and 86.7%, 63.8%, 97.3% in group II, respectively. There was no statistical significance in terms of local control, disease- free survival, overall survival and complication rates between the two treatment schedules which could be observed. Seven patients in group I developed acute grade 2-4 GI toxicities and two patients in group II. In GU toxicities, there were three patients in group I and three patients in group II who developed grade 2-4 toxicities. In late toxicity, no patient developed grade 3-4 GU toxicities in group I while two patients developed grade 3-4 GU toxicities in group II. In GI toxicities, there were five and six patients in group I and group II, respectively, who developed grade 3-4 severity. Both HDR schedules seem to be safe and effective for the treatment of locally advanced cervical cancer.en_US
dc.subjectEnvironmental Scienceen_US
dc.subjectMedicineen_US
dc.subjectPhysics and Astronomyen_US
dc.titleThe effects of two HDR brachytherapy schedules in locally advanced cervical cancer treated with concurrent chemoradiation: A study from Chiang Mai, Thailanden_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Radiation Researchen_US
article.volume53en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsChristian-Albrechts-Universitat zu Kielen_US
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