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Efficacy of intensity-modulated radiotherapy with concurrent carboplatin in nasopharyngeal carcinoma
BACKGROUND. The aim of the prospective phase II study was to evaluate the efficacy and toxicities of concurrent carboplatin with intensity-modulated radiotherapy (IMRT) in the treatment of nasopharyngeal carcinoma (NPC). PATIENTS AND METHODS. Between October 2005 and November 2011, 73 stage II–IVB N...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Versita, Warsaw
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387992/ https://www.ncbi.nlm.nih.gov/pubmed/26029027 http://dx.doi.org/10.2478/raon-2014-0044 |
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author | Songthong, Anussara Chakkabat, Chakkapong Kannarunimit, Danita Lertbutsayanukul, Chawalit |
author_facet | Songthong, Anussara Chakkabat, Chakkapong Kannarunimit, Danita Lertbutsayanukul, Chawalit |
author_sort | Songthong, Anussara |
collection | PubMed |
description | BACKGROUND. The aim of the prospective phase II study was to evaluate the efficacy and toxicities of concurrent carboplatin with intensity-modulated radiotherapy (IMRT) in the treatment of nasopharyngeal carcinoma (NPC). PATIENTS AND METHODS. Between October 2005 and November 2011, 73 stage II–IVB NPC patients received IMRT 70 Gy concurrently with three cycles of carboplatin (AUC 5) every three weeks, followed by three cycles of adjuvant carboplatin (AUC 5) and 5-FU (1,000 mg/m(2)/day for four days) every four weeks. All patients were evaluated for tumour response using response evaluation criteria in solid tumour (RECIST) criteria, survival analysis using Kaplan-Meier methods, and toxicities according to common terminology criteria for adverse events (CTCAE) version 4.0. RESULTS. At three months after chemoradiation, 82.2% and 17.8% of patients achieved complete and partial response, respectively. With a median follow-up of 48.1 months (1.3–97.8 months), 9.6% and 17.8% had local recurrence and distant metastasis, respectively. The median survival was not reached. A three-year overall survival was 83.6% and a progression-free survival was 65.3%. Regarding treatment compliance, 97.2%, 68.5% and 69.8% completed radiation treatment, concurrent carboplatin and adjuvant chemotherapy, respectively. Grade 3–4 acute toxicities were oral mucositis (16.4%), dysphagia (16.4%), xerostomia (15.1%) and haematotoxicity (6.8%). CONCLUSIONS. Carboplatin concurrently with IMRT provided excellent tumour response, manageable toxicities and good compliance. This should be considered as an alternative treatment for NPC patients. |
format | Online Article Text |
id | pubmed-4387992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Versita, Warsaw |
record_format | MEDLINE/PubMed |
spelling | pubmed-43879922015-06-01 Efficacy of intensity-modulated radiotherapy with concurrent carboplatin in nasopharyngeal carcinoma Songthong, Anussara Chakkabat, Chakkapong Kannarunimit, Danita Lertbutsayanukul, Chawalit Radiol Oncol Research Article BACKGROUND. The aim of the prospective phase II study was to evaluate the efficacy and toxicities of concurrent carboplatin with intensity-modulated radiotherapy (IMRT) in the treatment of nasopharyngeal carcinoma (NPC). PATIENTS AND METHODS. Between October 2005 and November 2011, 73 stage II–IVB NPC patients received IMRT 70 Gy concurrently with three cycles of carboplatin (AUC 5) every three weeks, followed by three cycles of adjuvant carboplatin (AUC 5) and 5-FU (1,000 mg/m(2)/day for four days) every four weeks. All patients were evaluated for tumour response using response evaluation criteria in solid tumour (RECIST) criteria, survival analysis using Kaplan-Meier methods, and toxicities according to common terminology criteria for adverse events (CTCAE) version 4.0. RESULTS. At three months after chemoradiation, 82.2% and 17.8% of patients achieved complete and partial response, respectively. With a median follow-up of 48.1 months (1.3–97.8 months), 9.6% and 17.8% had local recurrence and distant metastasis, respectively. The median survival was not reached. A three-year overall survival was 83.6% and a progression-free survival was 65.3%. Regarding treatment compliance, 97.2%, 68.5% and 69.8% completed radiation treatment, concurrent carboplatin and adjuvant chemotherapy, respectively. Grade 3–4 acute toxicities were oral mucositis (16.4%), dysphagia (16.4%), xerostomia (15.1%) and haematotoxicity (6.8%). CONCLUSIONS. Carboplatin concurrently with IMRT provided excellent tumour response, manageable toxicities and good compliance. This should be considered as an alternative treatment for NPC patients. Versita, Warsaw 2015-03-25 /pmc/articles/PMC4387992/ /pubmed/26029027 http://dx.doi.org/10.2478/raon-2014-0044 Text en Copyright © by Association of Radiology & Oncology http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Research Article Songthong, Anussara Chakkabat, Chakkapong Kannarunimit, Danita Lertbutsayanukul, Chawalit Efficacy of intensity-modulated radiotherapy with concurrent carboplatin in nasopharyngeal carcinoma |
title | Efficacy of intensity-modulated radiotherapy with concurrent carboplatin in nasopharyngeal carcinoma |
title_full | Efficacy of intensity-modulated radiotherapy with concurrent carboplatin in nasopharyngeal carcinoma |
title_fullStr | Efficacy of intensity-modulated radiotherapy with concurrent carboplatin in nasopharyngeal carcinoma |
title_full_unstemmed | Efficacy of intensity-modulated radiotherapy with concurrent carboplatin in nasopharyngeal carcinoma |
title_short | Efficacy of intensity-modulated radiotherapy with concurrent carboplatin in nasopharyngeal carcinoma |
title_sort | efficacy of intensity-modulated radiotherapy with concurrent carboplatin in nasopharyngeal carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387992/ https://www.ncbi.nlm.nih.gov/pubmed/26029027 http://dx.doi.org/10.2478/raon-2014-0044 |
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