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Pilot trial of endoscopic ultrasound-guided interstitial chemoradiation of UICC-T4 pancreatic cancer

BACKGROUND AND AIMS: Both interstitial brachytherapy and interstitial chemotherapy are effective in improving local control in patients with local UICC-T4 pancreatic cancer. In this study, we report the results of endoscopic ultrasound (EUS)-guided interstitial chemoradiation (EUS-ICR) in patients w...

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Autores principales: Sun, Siyu, Ge, Nan, Wang, Sheng, Liu, Xiang, Wang, Guoxin, Guo, Jintao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062203/
https://www.ncbi.nlm.nih.gov/pubmed/24949334
http://dx.doi.org/10.7178/eus.01.007
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author Sun, Siyu
Ge, Nan
Wang, Sheng
Liu, Xiang
Wang, Guoxin
Guo, Jintao
author_facet Sun, Siyu
Ge, Nan
Wang, Sheng
Liu, Xiang
Wang, Guoxin
Guo, Jintao
author_sort Sun, Siyu
collection PubMed
description BACKGROUND AND AIMS: Both interstitial brachytherapy and interstitial chemotherapy are effective in improving local control in patients with local UICC-T4 pancreatic cancer. In this study, we report the results of endoscopic ultrasound (EUS)-guided interstitial chemoradiation (EUS-ICR) in patients with advanced pancreatic cancer, with respect to tumor response, clinical response, safety, and complications. PATIENTS AND METHODS: A total of 8 patients (3 men, 5 women; median age of 69) with T4 pancreatic adenocarcinoma were the subjects of this study. A mean of 18 radioactive seeds and 36 intratumoral implants for sustained delivery of 5-fluorouracil in each patient were implanted into the tumors using EUS-guided needle puncture. The mean total implanted radioactive activity was 13.68 mCi, the mean total dose of intratumoral 5-fluorouracil was 3.6 g, and the mean volume of implants was 28 cm(3). The conditions of the patients were followed-up by examination and imaging tests every two months. Clinical endpoints included the Karnofsky performance status, pain response, tumor response (assessed by computed tomography and/or EUS), and survival. RESULTS: During a median follow-up period of 8.3 months, the objective tumor response was classified as “partial” in 1 of 8 patients (with a median duration of partial response of 3 months), “minimal” in 2 patients, and indicative of “stable disease”, in 3 of 8 patients. Clinical benefit was shown in 4 of 8 patients, which was mostly due to pain reduction, and lasted for 3.5 months. No local complications or hematologic toxicity occurred. CONCLUSIONS: EUS-ICR had a moderate local anti-tumor effect, showed some clinical benefits in 4 of the 8 patients, and was well tolerated by all the patients in this study.
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spelling pubmed-40622032014-06-19 Pilot trial of endoscopic ultrasound-guided interstitial chemoradiation of UICC-T4 pancreatic cancer Sun, Siyu Ge, Nan Wang, Sheng Liu, Xiang Wang, Guoxin Guo, Jintao Endosc Ultrasound Original Article BACKGROUND AND AIMS: Both interstitial brachytherapy and interstitial chemotherapy are effective in improving local control in patients with local UICC-T4 pancreatic cancer. In this study, we report the results of endoscopic ultrasound (EUS)-guided interstitial chemoradiation (EUS-ICR) in patients with advanced pancreatic cancer, with respect to tumor response, clinical response, safety, and complications. PATIENTS AND METHODS: A total of 8 patients (3 men, 5 women; median age of 69) with T4 pancreatic adenocarcinoma were the subjects of this study. A mean of 18 radioactive seeds and 36 intratumoral implants for sustained delivery of 5-fluorouracil in each patient were implanted into the tumors using EUS-guided needle puncture. The mean total implanted radioactive activity was 13.68 mCi, the mean total dose of intratumoral 5-fluorouracil was 3.6 g, and the mean volume of implants was 28 cm(3). The conditions of the patients were followed-up by examination and imaging tests every two months. Clinical endpoints included the Karnofsky performance status, pain response, tumor response (assessed by computed tomography and/or EUS), and survival. RESULTS: During a median follow-up period of 8.3 months, the objective tumor response was classified as “partial” in 1 of 8 patients (with a median duration of partial response of 3 months), “minimal” in 2 patients, and indicative of “stable disease”, in 3 of 8 patients. Clinical benefit was shown in 4 of 8 patients, which was mostly due to pain reduction, and lasted for 3.5 months. No local complications or hematologic toxicity occurred. CONCLUSIONS: EUS-ICR had a moderate local anti-tumor effect, showed some clinical benefits in 4 of the 8 patients, and was well tolerated by all the patients in this study. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC4062203/ /pubmed/24949334 http://dx.doi.org/10.7178/eus.01.007 Text en Copyright: © Endoscopic Ultrasound http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sun, Siyu
Ge, Nan
Wang, Sheng
Liu, Xiang
Wang, Guoxin
Guo, Jintao
Pilot trial of endoscopic ultrasound-guided interstitial chemoradiation of UICC-T4 pancreatic cancer
title Pilot trial of endoscopic ultrasound-guided interstitial chemoradiation of UICC-T4 pancreatic cancer
title_full Pilot trial of endoscopic ultrasound-guided interstitial chemoradiation of UICC-T4 pancreatic cancer
title_fullStr Pilot trial of endoscopic ultrasound-guided interstitial chemoradiation of UICC-T4 pancreatic cancer
title_full_unstemmed Pilot trial of endoscopic ultrasound-guided interstitial chemoradiation of UICC-T4 pancreatic cancer
title_short Pilot trial of endoscopic ultrasound-guided interstitial chemoradiation of UICC-T4 pancreatic cancer
title_sort pilot trial of endoscopic ultrasound-guided interstitial chemoradiation of uicc-t4 pancreatic cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062203/
https://www.ncbi.nlm.nih.gov/pubmed/24949334
http://dx.doi.org/10.7178/eus.01.007
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