Modified transarterial chemoembolization with locoregional administration of sorafenib for treating hepatocellular carcinoma
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Modified transarterial chemoembolization with locoregional administration of sorafenib for treating hepatocellular carcinoma : feasibility, efficacy, and safety in the VX-2 rabbit liver tumor model. / Seidensticker, Max; Streit, Sebastian; Nass, Norbert; Wybranski, Christian; Jürgens, Julian; Brauner, Jan; Schulz, Nadine; Kalinski, Thomas; Seidensticker, Ricarda; Garlipp, Benjamin; Steffen, Ingo; Ricke, Jens; Dudeck, Oliver.
In: DIAGN INTERV RADIOL, Vol. 22, No. 4, 23.06.2016, p. 378-84.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Modified transarterial chemoembolization with locoregional administration of sorafenib for treating hepatocellular carcinoma
T2 - feasibility, efficacy, and safety in the VX-2 rabbit liver tumor model
AU - Seidensticker, Max
AU - Streit, Sebastian
AU - Nass, Norbert
AU - Wybranski, Christian
AU - Jürgens, Julian
AU - Brauner, Jan
AU - Schulz, Nadine
AU - Kalinski, Thomas
AU - Seidensticker, Ricarda
AU - Garlipp, Benjamin
AU - Steffen, Ingo
AU - Ricke, Jens
AU - Dudeck, Oliver
PY - 2016/6/23
Y1 - 2016/6/23
N2 - PURPOSE: We aimed to assess the feasibility, efficacy and safety of a local application of sorafenib within a conventional transarterial chemoembolization in the VX-2 tumor-bearing rabbit model.METHODS: VX-2 tumors were induced in the left liver lobe of 10 New Zealand White rabbits. After two weeks, growth was verified by contrast-enhanced computed tomography (CT). Five rabbits were treated by transarterial chemoembolization using an emulsion of sorafenib and ethiodized oil (referred to as SORATACE; n=5). Rabbits receiving oral sorafenib for two weeks (n=2) and untreated rabbits (n=3) served as controls. After two weeks, contrast-enhanced CT was performed, followed by animal necropsy.RESULTS: The change in tumor diameter between baseline and follow-up was significantly different in the SORATACE group compared with the other groups; tumor shrinkage was observed in the SORATACE group only (P = 0.016). In both control groups, preserved hypervascularity was seen in the follow-up CT in all but one tumor. All tumors in the SORATACE group were devascularized in the follow-up CT. Importantly, substantial parenchymal damage in nontargeted areas of the tumor-bearing liver lobe was seen in rabbits treated with SORATACE.CONCLUSION: SORATACE demonstrated high efficacy in the treatment of experimental VX-2 liver tumors but was also associated with substantial liver parenchymal toxicity.
AB - PURPOSE: We aimed to assess the feasibility, efficacy and safety of a local application of sorafenib within a conventional transarterial chemoembolization in the VX-2 tumor-bearing rabbit model.METHODS: VX-2 tumors were induced in the left liver lobe of 10 New Zealand White rabbits. After two weeks, growth was verified by contrast-enhanced computed tomography (CT). Five rabbits were treated by transarterial chemoembolization using an emulsion of sorafenib and ethiodized oil (referred to as SORATACE; n=5). Rabbits receiving oral sorafenib for two weeks (n=2) and untreated rabbits (n=3) served as controls. After two weeks, contrast-enhanced CT was performed, followed by animal necropsy.RESULTS: The change in tumor diameter between baseline and follow-up was significantly different in the SORATACE group compared with the other groups; tumor shrinkage was observed in the SORATACE group only (P = 0.016). In both control groups, preserved hypervascularity was seen in the follow-up CT in all but one tumor. All tumors in the SORATACE group were devascularized in the follow-up CT. Importantly, substantial parenchymal damage in nontargeted areas of the tumor-bearing liver lobe was seen in rabbits treated with SORATACE.CONCLUSION: SORATACE demonstrated high efficacy in the treatment of experimental VX-2 liver tumors but was also associated with substantial liver parenchymal toxicity.
KW - Animals
KW - Carcinoma, Hepatocellular
KW - Cell Line, Tumor
KW - Chemoembolization, Therapeutic
KW - Drug Administration Schedule
KW - Female
KW - Liver Neoplasms
KW - Neoplasm Transplantation
KW - Niacinamide
KW - Phenylurea Compounds
KW - Rabbits
KW - Tomography, X-Ray Computed
KW - Treatment Outcome
KW - Tumor Burden
KW - Journal Article
U2 - 10.5152/dir.2016.15462
DO - 10.5152/dir.2016.15462
M3 - SCORING: Journal article
C2 - 27328720
VL - 22
SP - 378
EP - 384
JO - DIAGN INTERV RADIOL
JF - DIAGN INTERV RADIOL
SN - 1305-3825
IS - 4
ER -