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Efficacy of minimally invasive therapies on unresectable pancreatic cancer

For patients with unresectable pancreatic cancer, current chemotherapies have negligible survival benefits. Thus, developing effective minimally invasive therapies is currently underway. This study was conducted to evaluate the efficacy of transarterial chemoembolization plus radiofrequency ablation...

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Autores principales: Huang, Zhi-Mei, Pan, Chang-Chuan, Wu, Pei-Hong, Zhao, Ming, Li, Wang, Huang, Zi-Lin, Yi, Rui-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sun Yat-sen University Cancer Center 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845623/
https://www.ncbi.nlm.nih.gov/pubmed/22958741
http://dx.doi.org/10.5732/cjc.012.10093
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author Huang, Zhi-Mei
Pan, Chang-Chuan
Wu, Pei-Hong
Zhao, Ming
Li, Wang
Huang, Zi-Lin
Yi, Rui-Yang
author_facet Huang, Zhi-Mei
Pan, Chang-Chuan
Wu, Pei-Hong
Zhao, Ming
Li, Wang
Huang, Zi-Lin
Yi, Rui-Yang
author_sort Huang, Zhi-Mei
collection PubMed
description For patients with unresectable pancreatic cancer, current chemotherapies have negligible survival benefits. Thus, developing effective minimally invasive therapies is currently underway. This study was conducted to evaluate the efficacy of transarterial chemoembolization plus radiofrequency ablation and/or (125)I radioactive seed implantation on unresectable pancreatic cancer. We analyzed the outcome of 71 patients with unresectable pancreatic carcinoma who underwent chemoembolization plus radiofrequency ablation and/or radioactive seed implantation. Of the 71 patients, the median survival was 11 months, and the 1-, 2-, and 3-year overall survival rates were 32.4%, 9.9%, and 6.6% respectively. Patients who had no metastasis, who had oligonodular liver metastases (≤3 lesions), and who had multinodular liver metastases (>3 lesions) had median survival of 12, 18, and 8 months, respectively, and 1-year overall survival rates of 50.0%, 68.8%, and 5.7%, respectively. Although the survival of patients without liver metastases was worse than that of patients with oligonodular liver metastasis, the result was not significant (P = 0.239). In contrast, the metastasis-negative patients had significantly better survival than did patients with multinodular liver metastases (P < 0.001). Patients with oligonodular liver lesions had a significanthg longer median survival than did patients with multinodular lesions (P < 0.001). In conclusion, combined minimally invasive therapies had good efficacy on unresectable pancreatic cancer and resulted in a good control of liver metastases. In addition, the number of liver metastases was a significant factor in predicting prognosis and response to treatment.
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spelling pubmed-38456232013-12-11 Efficacy of minimally invasive therapies on unresectable pancreatic cancer Huang, Zhi-Mei Pan, Chang-Chuan Wu, Pei-Hong Zhao, Ming Li, Wang Huang, Zi-Lin Yi, Rui-Yang Chin J Cancer Original Article For patients with unresectable pancreatic cancer, current chemotherapies have negligible survival benefits. Thus, developing effective minimally invasive therapies is currently underway. This study was conducted to evaluate the efficacy of transarterial chemoembolization plus radiofrequency ablation and/or (125)I radioactive seed implantation on unresectable pancreatic cancer. We analyzed the outcome of 71 patients with unresectable pancreatic carcinoma who underwent chemoembolization plus radiofrequency ablation and/or radioactive seed implantation. Of the 71 patients, the median survival was 11 months, and the 1-, 2-, and 3-year overall survival rates were 32.4%, 9.9%, and 6.6% respectively. Patients who had no metastasis, who had oligonodular liver metastases (≤3 lesions), and who had multinodular liver metastases (>3 lesions) had median survival of 12, 18, and 8 months, respectively, and 1-year overall survival rates of 50.0%, 68.8%, and 5.7%, respectively. Although the survival of patients without liver metastases was worse than that of patients with oligonodular liver metastasis, the result was not significant (P = 0.239). In contrast, the metastasis-negative patients had significantly better survival than did patients with multinodular liver metastases (P < 0.001). Patients with oligonodular liver lesions had a significanthg longer median survival than did patients with multinodular lesions (P < 0.001). In conclusion, combined minimally invasive therapies had good efficacy on unresectable pancreatic cancer and resulted in a good control of liver metastases. In addition, the number of liver metastases was a significant factor in predicting prognosis and response to treatment. Sun Yat-sen University Cancer Center 2013-06 /pmc/articles/PMC3845623/ /pubmed/22958741 http://dx.doi.org/10.5732/cjc.012.10093 Text en Chinese Journal of Cancer 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-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Original Article
Huang, Zhi-Mei
Pan, Chang-Chuan
Wu, Pei-Hong
Zhao, Ming
Li, Wang
Huang, Zi-Lin
Yi, Rui-Yang
Efficacy of minimally invasive therapies on unresectable pancreatic cancer
title Efficacy of minimally invasive therapies on unresectable pancreatic cancer
title_full Efficacy of minimally invasive therapies on unresectable pancreatic cancer
title_fullStr Efficacy of minimally invasive therapies on unresectable pancreatic cancer
title_full_unstemmed Efficacy of minimally invasive therapies on unresectable pancreatic cancer
title_short Efficacy of minimally invasive therapies on unresectable pancreatic cancer
title_sort efficacy of minimally invasive therapies on unresectable pancreatic cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845623/
https://www.ncbi.nlm.nih.gov/pubmed/22958741
http://dx.doi.org/10.5732/cjc.012.10093
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