scholarly journals Systemic Therapy for Advanced Hepatocellular Carcinoma: Targeted Therapy and Immunotherapy

2018 ◽  
Vol 18 (1) ◽  
pp. 17-22 ◽  
Author(s):  
Bo Hyun Kim ◽  
Joong-Won Park
2008 ◽  
Vol 14 (42) ◽  
pp. 6546 ◽  
Author(s):  
Ming Jiang ◽  
Fei Liu ◽  
Wu-Jun Xiong ◽  
Lan Zhong ◽  
Xi-Mei Chen

Author(s):  
Yung-Yeh Su ◽  
Chia-Chen Li ◽  
Yih-Jyh Lin ◽  
Chiun Hsu

AbstractAdvancement in systemic therapy, particularly immune checkpoint inhibitor (ICI)-based combination regimens, has transformed the treatment landscape for patients with advanced hepatocellular carcinoma (HCC). The advancement in systemic therapy also provides new opportunities of reducing recurrence after curative therapy through adjuvant therapy or improving resectability through neoadjuvant therapy. Improved recurrence-free survival by adjuvant or neoadjuvant ICI-based therapy has been reported in other cancer types. In this article, developments of systemic therapy in adjuvant and neoadjuvant settings for HCC were reviewed. The design of adjuvant and neoadjuvant therapy using ICI-based regimens and potential challenges of trial conduct and result analysis was discussed. Results from these trials may extend the therapeutic benefit of ICI-based systemic therapy beyond the advanced-stage disease and lead to a new era of multidisciplinary management for HCC.


2016 ◽  
Vol 34 (15_suppl) ◽  
pp. 4075-4075
Author(s):  
Dae-Won Lee ◽  
Myoung-Jin Jang ◽  
Kyung-Hun Lee ◽  
Tae-Yong Kim ◽  
Sae-Won Han ◽  
...  

2010 ◽  
Vol 17 (2) ◽  
pp. 120-129 ◽  
Author(s):  
Jennifer L. Giglia ◽  
Scott J. Antonia ◽  
Lawrence B. Berk ◽  
Salvador Bruno ◽  
Sophie Dessureault ◽  
...  

2017 ◽  
Vol 35 (4_suppl) ◽  
pp. 454-454
Author(s):  
Kyung-Hun Lee ◽  
Dae-Won Lee ◽  
Myoung-Jin Jang ◽  
Tae-Yong Kim ◽  
Sae-Won Han ◽  
...  

454 Background: Time to progression (TTP) is suggested as a reliable endpoint compared to progression free survival (PFS) in the clinical trials of hepatocellular carcinoma (HCC). However, the correlation between TTP and overall survival (OS) has never been studied. Methods: We searched Pubmed and Embase data to obtain data source. Eligible studies were randomized controlled phase III trials which evaluated the efficacy of systemic chemotherapy or molecular targeted therapy in advanced HCC. The association of treatment effects as shown by the hazard ratio (HR) of TTP and OS in each trial was assessed by Spearman rank correlation coefficient ( rs) and linear regression analysis. The association between median TTP and OS was also investigated. Results: Nine studies with a total of 18 treatment arms and 6318 patients were included. Incremental benefit from the study treatment in TTP from each trial was correlated with incremental benefit in OS. The rs value and R2 value between log (HRTTP) and log (HROS) was 0.73 (95% CI 0.12 – 0.94, p = 0.024) and 0.57. The minimum TTP effect to predict a treatment effect on OS was 0.63. Median TTP was associated with median OS. The rs value between TTP and OS was 0.73 (95% confidence interval (CI) 0.40 – 0.89, p < 0.001) and the corresponding R2 was 0.42. Conclusions: Our study results suggest that TTP could be used as a surrogate marker for OS in the clinical trials of advanced HCC. However, the results suggest modest correlation between treatment effects on TTP and OS. Along with individual-level analysis more evidences are needed to confirm our finding.


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