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Intratumoral radiofrequency hyperthermia-enhanced direct chemotherapy of pancreatic cancer

PURPOSE: To investigate the technical feasibility of using ultrasound-guided intratumoral radiofrequency hyperthermia (RFH) to enhance local chemotherapy of rat orthotopic pancreatic cancers. MATERIALS AND METHODS: Orthotopic pancreatic cancer masses were established by inoculating luciferase/mCherr...

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Autores principales: Bai, Zhibin, Shi, Yaoping, Wang, Jianfeng, Qiu, Longhua, Monroe, Eric J., Teng, Gaojun, Zhang, Feng, Yang, Xiaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356906/
https://www.ncbi.nlm.nih.gov/pubmed/27690303
http://dx.doi.org/10.18632/oncotarget.12295
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author Bai, Zhibin
Shi, Yaoping
Wang, Jianfeng
Qiu, Longhua
Monroe, Eric J.
Teng, Gaojun
Zhang, Feng
Yang, Xiaoming
author_facet Bai, Zhibin
Shi, Yaoping
Wang, Jianfeng
Qiu, Longhua
Monroe, Eric J.
Teng, Gaojun
Zhang, Feng
Yang, Xiaoming
author_sort Bai, Zhibin
collection PubMed
description PURPOSE: To investigate the technical feasibility of using ultrasound-guided intratumoral radiofrequency hyperthermia (RFH) to enhance local chemotherapy of rat orthotopic pancreatic cancers. MATERIALS AND METHODS: Orthotopic pancreatic cancer masses were established by inoculating luciferase/mCherry labeled-pancreatic cancer cells into the pancreatic tails of Lewis model rats via a laparotomy approach. Twenty-four rats with pancreatic cancer and 24 mice with subcutaneous pancreatic cancer xenografts in four study groups (n = 6/group) received various treatments: i) combination therapy of intratumoral MR imaging-heating-guidewire-mediated RFH (42(o)C) plus local chemotherapy (gemcitabine); ii) intratumoral chemotherapy alone; iii) RFH alone; and (iv)phosphate-buffered saline (PBS). Transcutaneous ultrasound imaging was used to guide the treatment and subsequently follow changes in tumor sizes. Bioluminescence optical imaging was performed to follow photon signal changes. Sonographic and optical findings were correlated with histology at 14 days. RESULTS: Optical imaging demonstrated a significantly decreased bioluminescence signal in mice with combination therapy group, compared with the other control groups (0.51±0.18 VS 1.6±0.4 VS 3.18±0.9 VS 3.5±0.96, p < 0.05). Ultrasound imaging showed the smallest tumor volumes of both mice and rat group with the combination therapy, compared with other control groups (0.62±0.16 VS 1.25±0.19 VS 2.28±0.25 VS 2.64±0.26, p < 0.05) and (0.75±0.18 VS 1.31±0.30 VS 1.61±0.28 VS 1.72±0.28, p < 0.05). Both imaging findings were confirmed by histologic correlation. CONCLUSION: Intratumoral RFH can augment the chemotherapeutic effect in an orthotopic pancreatic cancer model.
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spelling pubmed-53569062017-04-20 Intratumoral radiofrequency hyperthermia-enhanced direct chemotherapy of pancreatic cancer Bai, Zhibin Shi, Yaoping Wang, Jianfeng Qiu, Longhua Monroe, Eric J. Teng, Gaojun Zhang, Feng Yang, Xiaoming Oncotarget Clinical Research Paper PURPOSE: To investigate the technical feasibility of using ultrasound-guided intratumoral radiofrequency hyperthermia (RFH) to enhance local chemotherapy of rat orthotopic pancreatic cancers. MATERIALS AND METHODS: Orthotopic pancreatic cancer masses were established by inoculating luciferase/mCherry labeled-pancreatic cancer cells into the pancreatic tails of Lewis model rats via a laparotomy approach. Twenty-four rats with pancreatic cancer and 24 mice with subcutaneous pancreatic cancer xenografts in four study groups (n = 6/group) received various treatments: i) combination therapy of intratumoral MR imaging-heating-guidewire-mediated RFH (42(o)C) plus local chemotherapy (gemcitabine); ii) intratumoral chemotherapy alone; iii) RFH alone; and (iv)phosphate-buffered saline (PBS). Transcutaneous ultrasound imaging was used to guide the treatment and subsequently follow changes in tumor sizes. Bioluminescence optical imaging was performed to follow photon signal changes. Sonographic and optical findings were correlated with histology at 14 days. RESULTS: Optical imaging demonstrated a significantly decreased bioluminescence signal in mice with combination therapy group, compared with the other control groups (0.51±0.18 VS 1.6±0.4 VS 3.18±0.9 VS 3.5±0.96, p < 0.05). Ultrasound imaging showed the smallest tumor volumes of both mice and rat group with the combination therapy, compared with other control groups (0.62±0.16 VS 1.25±0.19 VS 2.28±0.25 VS 2.64±0.26, p < 0.05) and (0.75±0.18 VS 1.31±0.30 VS 1.61±0.28 VS 1.72±0.28, p < 0.05). Both imaging findings were confirmed by histologic correlation. CONCLUSION: Intratumoral RFH can augment the chemotherapeutic effect in an orthotopic pancreatic cancer model. Impact Journals LLC 2016-09-27 /pmc/articles/PMC5356906/ /pubmed/27690303 http://dx.doi.org/10.18632/oncotarget.12295 Text en Copyright: © 2017 Bai et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Bai, Zhibin
Shi, Yaoping
Wang, Jianfeng
Qiu, Longhua
Monroe, Eric J.
Teng, Gaojun
Zhang, Feng
Yang, Xiaoming
Intratumoral radiofrequency hyperthermia-enhanced direct chemotherapy of pancreatic cancer
title Intratumoral radiofrequency hyperthermia-enhanced direct chemotherapy of pancreatic cancer
title_full Intratumoral radiofrequency hyperthermia-enhanced direct chemotherapy of pancreatic cancer
title_fullStr Intratumoral radiofrequency hyperthermia-enhanced direct chemotherapy of pancreatic cancer
title_full_unstemmed Intratumoral radiofrequency hyperthermia-enhanced direct chemotherapy of pancreatic cancer
title_short Intratumoral radiofrequency hyperthermia-enhanced direct chemotherapy of pancreatic cancer
title_sort intratumoral radiofrequency hyperthermia-enhanced direct chemotherapy of pancreatic cancer
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356906/
https://www.ncbi.nlm.nih.gov/pubmed/27690303
http://dx.doi.org/10.18632/oncotarget.12295
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