Published online May 28, 2016. doi: 10.3748/wjg.v22.i20.4835
Peer-review started: February 28, 2016
First decision: March 21, 2016
Revised: March 29, 2016
Accepted: April 20, 2016
Article in press: April 20, 2016
Published online: May 28, 2016
Processing time: 82 Days and 22.6 Hours
Hepatocellular carcinoma (HCC) is one of the major causes of morbidity and mortality in patients with chronic liver disease. Transarterial chemoembolization (TACE) can significantly improve the survival rate of patients with HCC and is the first treatment choice for patients who are not suitable for surgical resections. The evaluation of the response to TACE treatment affects not only the assessment of the therapy efficacy but also the development of the next step in the treatment plan. The use of imaging to examine changes in tumor volume to assess the response of solid tumors to treatment has been controversial. In recent years, the emergence of new imaging technology has made it possible to observe the response of tumors to treatment prior to any morphological changes. In this article, the advances in studies reporting the use of computed tomography perfusion imaging, diffusion-weighted magnetic resonance imaging (MRI), intravoxel incoherent motion, diffusion kurtosis imaging, magnetic resonance spectroscopy, magnetic resonance perfusion-weighted imaging, blood oxygen level-dependent MRI, positron emission tomography (PET)/computed tomography and PET/MRI to assess the TACE treatment response are reviewed.
Core tip: Imaging studies play an important role in the evaluation of the response to transarterial chemoembolization treatment. The use of imaging to examine changes in tumor size to assess the response of solid tumors to treatment has been controversial. In recent years, the emergence of new imaging technologies has made it possible to observe the response of tumors to treatment prior to any morphological changes. In this article, we present a summary of the most recent information on the role of imaging in assessing the treatment response in hepatocellular carcinomas.