2012
DOI: 10.1007/s00330-011-2368-z
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Conventional transarterial chemoembolisation in combination with sorafenib for patients with hepatocellular carcinoma: a pilot study

Abstract: • Transarterial chemoembolisation (TACE) is widely used in patients with hepatocellular carcinoma (HCC) • Various antiangiogenic and other agents have been used to augment this treatment • We tested lipiodol-TACE with bilirubin-adjusted doxorubicin dosing in combination with sorafenib • This trial was stopped prematurely because of safety reasons • Our safety results do not support the combination of sorafenib with this TACE regimen.

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Cited by 39 publications
(21 citation statements)
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“…Despite the positive outcomes reported with the combined therapy, a clinical trial that enrolled a small number of patients was stopped prematurely due to adverse events (AE) and safety concerns with the combination therapy of high-dose doxorubicinbased TACE regimen and sorafenib [31] .…”
Section: Introductionmentioning
confidence: 99%
“…Despite the positive outcomes reported with the combined therapy, a clinical trial that enrolled a small number of patients was stopped prematurely due to adverse events (AE) and safety concerns with the combination therapy of high-dose doxorubicinbased TACE regimen and sorafenib [31] .…”
Section: Introductionmentioning
confidence: 99%
“…At 6 months, seven patients presented complete (two) or partial (five) responses, and one had stable disease. Median overall survival was 10.6 months (95% CI: 5.2 -16 months) [15].…”
Section: Discussionmentioning
confidence: 99%
“…However, the addition of sorafenib failed to prolong TTP (5.4 months vs. 3.7 months; HR = 0.87; P = 0.252) [58]. Subsequently, a number of phase II trials evaluating the efficacy and safety of conventional TACE or TACE with doxorubicin-eluting beads (DEB) with concurrent sorafenib (which started within 14 days before or after TACE was carried out) revealed inconsistent results [59,60,61,62,63,64]. The diversity of study designs created confounding factors including primary endpoints, patient populations, TACE procedures, timing of randomization, and drug administration may account for these conflicting results [69].…”
Section: Clinical Trials Of Molecular Targeted Therapy In Combinationmentioning
confidence: 99%
“…Data from clinical trials on a variety of molecular targeted therapies in combination with locoregional therapy are shown in table 2[58,59,60,61,62,63,64,65,66,67,68]. …”
Section: Clinical Trials Of Molecular Targeted Therapy In Combinationmentioning
confidence: 99%