Research Article Details

Article ID: A30789
PMID: 31779702
Source: J Immunother Cancer
Title: Immunotherapy response evaluation with magnetic resonance elastography (MRE) in advanced HCC.
Abstract: BACKGROUND: Currently, there are no imaging predictors of immunotherapy outcome in hepatocellular carcinoma (HCC). The study aim was to determine if stiffness changes measured by magnetic resonance elastography (MRE) can be a predictor of immunotherapy response in patients with advanced HCC. MATERIALS AND METHODS: This was a prospective study of 15 patients with biopsy proven-advanced HCC treated with Pembrolizumab. All patients had liver MRE and liver biopsy at baseline and at 6&#8201;weeks of therapy. Change in HCC stiffness on MRE was compared with overall survival (OS), time to disease progression (TTP), and number of intratumoral CD3+ T lymphocytes. Analysis was performed using descriptive statistics and Spearman correlation (R); p-value&#8201;<&#8201;0.05 was considered statistically significant. RESULTS: Nine patients were evaluable. Median age was 71&#8201;years (range, 54-78). Etiology of liver disease was HCV (n&#8201;=&#8201;4), HBV (n&#8201;=&#8201;1) and NASH (n&#8201;=&#8201;4). Median OS and TTP were 44&#8201;weeks and 13&#8201;weeks, respectively. Average baseline HCC stiffness and change in HCC stiffness were 5.0&#8201;kPa and 0.12&#8201;kPa, respectively. In contrast, average non-tumor liver stiffness was 3.2&#8201;kPa, and did not significantly change at 6&#8201;weeks (p&#8201;=&#8201;0.42). Average size of measured tumor and change in size were 4&#8201;cm and&#8201;-&#8201;0.32&#8201;cm, respectively. Change in HCC stiffness at 6&#8201;weeks correlated significantly with OS (R&#8201;=&#8201;0.81), and TTP (R&#8201;=&#8201;0.88,p&#8201;<&#8201;0.01). Abundance of intratumoral T lymphocytes on tumor biopsy correlated significantly with HCC stiffness (R&#8201;=&#8201;0.79,p&#8201;=&#8201;0.007). CONCLUSION: Our pilot MRE data suggests early change in tumor stiffness may be an indicator of immunotherapy response in patients with advanced HCC.
DOI: 10.1186/s40425-019-0766-y