Carcinoma, Hepatocellular Clinical Trial
Official title:
Fingerprint Characterization of Advanced HCC to Optimize Treatment Decisions and Enable an Early Prediction of Therapy Resistance (HCC Multiscale Trial-1)
This single center, open-label, uncontrolled, non-randomized observational study in patients with advanced HCC. The patients qualify either to a local treatment with transarterial chemoembolization (TACE) or to a systemic treatment with the multikinase inhibitor sorafenib. The aim of this feasibility study is to get a comprehensive image and molecular fingerprint of individual tumors, with the intention to govern therapy decisions. Furthermore, to improve the care of patients that get progressive disease under treatment, the investigators have to improve the investigators understanding of the development of therapy resistance, which will improve patient care at the time point of progressive disease. Therefore, the data of 20 patients in each group will be used to identify molecular and / or image patterns, that can be used to predict treatment responses and thus govern an optimized individual cancer treatment for patients with advanced HCC.
A single-center, open-label, uncontrolled, non-randomized clinical trial. The two treatment
groups to receive:
Group A Transarterial Chemoembolization (TACE): 20 patients that are treated with TACE will
get an image and molecular fingerprint of the tumor prior to the first treatment with TACE, a
second image fingerprint between week 2 - 4 after the first treatment with TACE, and a third
image and molecular fingerprint at the time point of progressive disease.
Group B Sorafenib: 20 patients that are treated with Sorafenib will get an image and
molecular fingerprint of the tumor prior to the first treatment, between week 2 and 3 after
the start of treatment and at the time point of progressive disease.
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