Carcinoma, Hepatocellular Clinical Trial
Official title:
A Prospective Study of Anti-PD-1 Inhibitors Therapy in Combination With Incomplete Thermal Ablation in Patients With Advanced Hepatocellular Carcinoma
The inhibition of programmed cell death protein 1 (PD-1) has shown promising antitumor activity in advanced hepatocellular carcinoma (HCC). Unfortunately, less than 20% of HCC have response. The effect of PD-1 blockade and incomplete thermal ablation in patients with advanced HCC is not yet clearly understood. This study aimed to analyze outcomes of advanced HCC treated with anti PD-1 inhibitors in combination with incomplete thermal ablation.
Hepatocellular carcinoma (HCC) is ranked as the third leading cause of cancer death both
worldwide and in the China. In the past decade, survivals of patients with advanced HCC or
those who have progressed diseases following locoregional treatments can be increased with
the multi-kinase inhibitor sorafenib, the first evidence identified drug for HCC. Recent
clinical trials further verified some novel tyrosine kinase inhibitors such as regorafenib
and cabozantinib, and two programmed cell death protein-1 (PD-1) immune checkpoint inhibitors
(ICIs), nivolumab and pembrolizumab, as useful therapies in second line setting following
sorafenib.
Advances in programmed cell death protein 1 (PD-1) blockade have shown an ORR of 15-17% and
median survival time of 12.9-15.0 months among patients with advanced HCC. Of these,
nivolumab and pembrolizumab have been accelerated approved as second-line treatment of
advanced HCC. Notably, patients who have tumor responses maintain long-lasting disease
control for 9.9-17months and still a large proportion of patients (81-83%) do not respond to
mono PD-1 blockade, which emphasizing the need to explore strategies to increase the efficacy
of immunotherapy.
An approach to expanding the benefit of ICIs may involve combinations with locoregional
therapy like radiofrequency ablation (RFA) and transarterial chemoembolization (TACE), such
treatments have been shown to boost tumor-specific T-cell response through release of TAAs
from HCC cells. The intent-to-treat population of this study was a subset of patients
receiving ongoing ICIs therapy for advanced HCC and is with stable disease or atypical
responses in different lesions of the same individuals.
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