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A safe and effective dose of cisplatin in hepatic arterial infusion chemotherapy for hepatocellular carcinoma

Cisplatin (CDDP) is an anticancer agent that is commonly used in hepatic arterial infusion (HAI) chemotherapy for hepatocellular carcinoma (HCC). This study aimed to clarify the safe and effective dose of CDDP in HAI for HCC. The hypervascular area was measured in 42 HCCs before and after HAI with C...

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Autores principales: Osaki, Akihiko, Suda, Takeshi, Kamimura, Kenya, Tsuchiya, Atsunori, Tamura, Yasushi, Takamura, Masaaki, Igarashi, Masato, Kawai, Hirokazu, Yamagiwa, Satoshi, Aoyagi, Yutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797567/
https://www.ncbi.nlm.nih.gov/pubmed/24133631
http://dx.doi.org/10.1002/cam4.55
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author Osaki, Akihiko
Suda, Takeshi
Kamimura, Kenya
Tsuchiya, Atsunori
Tamura, Yasushi
Takamura, Masaaki
Igarashi, Masato
Kawai, Hirokazu
Yamagiwa, Satoshi
Aoyagi, Yutaka
author_facet Osaki, Akihiko
Suda, Takeshi
Kamimura, Kenya
Tsuchiya, Atsunori
Tamura, Yasushi
Takamura, Masaaki
Igarashi, Masato
Kawai, Hirokazu
Yamagiwa, Satoshi
Aoyagi, Yutaka
author_sort Osaki, Akihiko
collection PubMed
description Cisplatin (CDDP) is an anticancer agent that is commonly used in hepatic arterial infusion (HAI) chemotherapy for hepatocellular carcinoma (HCC). This study aimed to clarify the safe and effective dose of CDDP in HAI for HCC. The hypervascular area was measured in 42 HCCs before and after HAI with CDDP. Serum platinum concentration was quantified in the peripheral and/or middle hepatic veins by atomic absorption spectrometry. The relation between the HCC response and CDDP dose was statistically analyzed. The multiple HCC nodules in an individual case generally demonstrated the same response to CDDP. The free-platinum concentration stayed relatively constant in the hepatic vein during HAI followed by a rapid decline, while total-platinum gradually increased then slowly disappeared over several days. After CDDP-HAI, 15 HCCs shrunk and 27 HCCs grew. The reduction rate in the shrunken nodules was tended to be correlated with CDDP dose after standardization with the target liver volume. On the other hand, the growth rate of the enlarged HCCs was significantly correlated with CDDP dose after normalization with creatinine clearance. These data support a recommendation of CDDP-HAI infusion where the amount of CDDP (mg) administered is less than patient creatinine clearance (mL/min/1.73 m(2)) upon an assumption of HCC doubling time of 90 days, and the targeted liver is smaller than 200 times the CDDP dose (mg). A further analysis is required to define appropriate injection speeds.
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spelling pubmed-37975672013-10-16 A safe and effective dose of cisplatin in hepatic arterial infusion chemotherapy for hepatocellular carcinoma Osaki, Akihiko Suda, Takeshi Kamimura, Kenya Tsuchiya, Atsunori Tamura, Yasushi Takamura, Masaaki Igarashi, Masato Kawai, Hirokazu Yamagiwa, Satoshi Aoyagi, Yutaka Cancer Med Clinical Cancer Research Cisplatin (CDDP) is an anticancer agent that is commonly used in hepatic arterial infusion (HAI) chemotherapy for hepatocellular carcinoma (HCC). This study aimed to clarify the safe and effective dose of CDDP in HAI for HCC. The hypervascular area was measured in 42 HCCs before and after HAI with CDDP. Serum platinum concentration was quantified in the peripheral and/or middle hepatic veins by atomic absorption spectrometry. The relation between the HCC response and CDDP dose was statistically analyzed. The multiple HCC nodules in an individual case generally demonstrated the same response to CDDP. The free-platinum concentration stayed relatively constant in the hepatic vein during HAI followed by a rapid decline, while total-platinum gradually increased then slowly disappeared over several days. After CDDP-HAI, 15 HCCs shrunk and 27 HCCs grew. The reduction rate in the shrunken nodules was tended to be correlated with CDDP dose after standardization with the target liver volume. On the other hand, the growth rate of the enlarged HCCs was significantly correlated with CDDP dose after normalization with creatinine clearance. These data support a recommendation of CDDP-HAI infusion where the amount of CDDP (mg) administered is less than patient creatinine clearance (mL/min/1.73 m(2)) upon an assumption of HCC doubling time of 90 days, and the targeted liver is smaller than 200 times the CDDP dose (mg). A further analysis is required to define appropriate injection speeds. Blackwell Publishing Ltd 2013-02 2013-02-03 /pmc/articles/PMC3797567/ /pubmed/24133631 http://dx.doi.org/10.1002/cam4.55 Text en Copyright © 2012 The Authors. Published by Blackwell Publishing Ltd. http://creativecommons.org/licenses/by/2.5/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Osaki, Akihiko
Suda, Takeshi
Kamimura, Kenya
Tsuchiya, Atsunori
Tamura, Yasushi
Takamura, Masaaki
Igarashi, Masato
Kawai, Hirokazu
Yamagiwa, Satoshi
Aoyagi, Yutaka
A safe and effective dose of cisplatin in hepatic arterial infusion chemotherapy for hepatocellular carcinoma
title A safe and effective dose of cisplatin in hepatic arterial infusion chemotherapy for hepatocellular carcinoma
title_full A safe and effective dose of cisplatin in hepatic arterial infusion chemotherapy for hepatocellular carcinoma
title_fullStr A safe and effective dose of cisplatin in hepatic arterial infusion chemotherapy for hepatocellular carcinoma
title_full_unstemmed A safe and effective dose of cisplatin in hepatic arterial infusion chemotherapy for hepatocellular carcinoma
title_short A safe and effective dose of cisplatin in hepatic arterial infusion chemotherapy for hepatocellular carcinoma
title_sort safe and effective dose of cisplatin in hepatic arterial infusion chemotherapy for hepatocellular carcinoma
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797567/
https://www.ncbi.nlm.nih.gov/pubmed/24133631
http://dx.doi.org/10.1002/cam4.55
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