Changes in Serum Growth Factors during Resistance to Atezolizumab Plus Bevacizumab Treatment in Patients with Unresectable Hepatocellular Carcinoma DOI Open Access
Zijian Yang, Goki Suda,

Osamu Maehara

et al.

Cancers, Journal Year: 2023, Volume and Issue: 15(3), P. 593 - 593

Published: Jan. 18, 2023

The possible mechanisms of resistance to atezolizumab/bevacizumab for unresectable HCC, and the subsequent response these therapies, remain underexplored. sequential changes in serum growth factors, including VEGF-A, VEGF-C, VEGF-D, ANG-2, FGF-19, HGF, EGF during HCC were evaluated 46 patients. Patients who experienced PD after CR, PR, or SD evaluated. A total 4, 9, 19, 14 patients showed SD, PD, respectively. Of 32 with disease control, 28 atezolizumab/bevacizumab. Baseline factor levels similar between without control those an objective response. Growth baseline best overall points (BOR) that FGF-19 significantly increased ANG2 decreased at BOR. BOR point VEGF-D compared Summarily, ANG-2 might contribute developing be target molecules salvage therapies.

Language: Английский

Alcohol and Hepatocellular Carcinoma DOI
Nghiem B. Ha, Francis Y. Yao

Clinics in Liver Disease, Journal Year: 2024, Volume and Issue: 28(4), P. 633 - 646

Published: July 23, 2024

Language: Английский

Citations

5

Lenvatinib as First-Line Treatment for Unresectable Hepatocellular Carcinoma: A Systematic Review and Meta-Analysis DOI Open Access
Shijie Wang, Yiting Wang, Jiangtao Yu

et al.

Cancers, Journal Year: 2022, Volume and Issue: 14(22), P. 5525 - 5525

Published: Nov. 10, 2022

Lenvatinib was approved in 2018 as a first-line treatment for patients with unresectable hepatocellular carcinoma (HCC). This systematic review and meta-analysis aimed to provide the most updated evidence about efficacy safety of lenvatinib HCC. An electronic search PubMed database, Web Science, Embase, Cochrane Library undertaken identify all relevant studies up May 2022. The pooled effect sizes were calculated based on random-effects model. One phase III randomized controlled trial 23 retrospective 2438 eligible analysis. For treated treatment, median overall survival (OS), progression-free (PFS), 1-year OS rate, PFS objective response rate (ORR), disease control (DCR) 11.36 months, 6.68 56.0%, 27.0%, 36.0% 75.0%, respectively. showed significantly superior compared sorafenib (HR OS, 0.85 HR PFS, 0.72; OR ORR, 4.25 DCR, 2.23). current study demonstrates that can better tumor responses benefits than HCC, comparable incidence adverse events.

Language: Английский

Citations

22

Clinical practice guidelines and real-life practice in hepatocellular carcinoma: A Japanese perspective DOI Creative Commons
Hironori Koga, Hideki Iwamoto, Hiroyuki Suzuki

et al.

Clinical and Molecular Hepatology, Journal Year: 2023, Volume and Issue: 29(2), P. 242 - 251

Published: March 21, 2023

Striking advances in systemic therapy for unresectable advanced hepatocellular carcinoma (HCC) have improved the average prognosis of patients with HCC. As a result, guidelines treatment HCC changed significantly. However, various issues emerged clinical practice. First, there is no established biomarker that can predict response to therapy. Second, regimen after primary therapy, including combined immunotherapy. Third, intermediate-stage These points make current ambiguous. In this review, we present Japanese diagnosis and based on latest evidence; introduce efforts mainly real-life practice update these guidelines; our perspectives future guidelines.

Language: Английский

Citations

12

The New Era of Systemic Treatment for Hepatocellular Carcinoma: From the First Line to the Optimal Sequence DOI Creative Commons

Maria Cerreto,

Ferdinando Cardone,

Lucia Cerrito

et al.

Current Oncology, Journal Year: 2023, Volume and Issue: 30(10), P. 8774 - 8792

Published: Sept. 26, 2023

Hepatocellular carcinoma (HCC) represents the most common primary liver cancer and is considered a major global health problem as one of leading causes cancer-related death in world. Due to increase life expectancy epidemiological growth specific risk factors, such metabolic dysfunction-associated steatotic disease (MASLD), incidence HCC growing globally, mortality rates are still high. Moreover, patients frequently present at an intermediate or advanced tumor stage, when curative treatments, surgical resection, transplantation ablation no longer applicable. In these cases, trans-arterial chemoembolization (TACE), radioembolization (TARE), systemic therapy only suitable options achieve control. The multi-kinase inhibitor Sorafenib has been treatment available for unresectable almost decade, but last couple years new therapeutic have emerged. Recent advances understanding interactions between its microenvironment, especially immune escape, led advent immunotherapy. Currently, first-line represented by combination checkpoint (ICI) Atezolizumab plus Bevacizumab, anti-vascular endothelial factor (VEGF) monoclonal antibody, many other ICIs investigated, Nivolumab, Pembrolizumab, Durvalumab Ipilimumab. However, second- third-line therapies, correct sequence treatments remains open not addressed studies. This explains urge find that can improve survival quality go beyond first line treatment. aim this paper offer complete overview recent innovations locally metastatic HCC, including emerging with particular focus on sequences. we will provide outlook possible future approaches who progress therapies.

Language: Английский

Citations

12

Changes in Serum Growth Factors during Resistance to Atezolizumab Plus Bevacizumab Treatment in Patients with Unresectable Hepatocellular Carcinoma DOI Open Access
Zijian Yang, Goki Suda,

Osamu Maehara

et al.

Cancers, Journal Year: 2023, Volume and Issue: 15(3), P. 593 - 593

Published: Jan. 18, 2023

The possible mechanisms of resistance to atezolizumab/bevacizumab for unresectable HCC, and the subsequent response these therapies, remain underexplored. sequential changes in serum growth factors, including VEGF-A, VEGF-C, VEGF-D, ANG-2, FGF-19, HGF, EGF during HCC were evaluated 46 patients. Patients who experienced PD after CR, PR, or SD evaluated. A total 4, 9, 19, 14 patients showed SD, PD, respectively. Of 32 with disease control, 28 atezolizumab/bevacizumab. Baseline factor levels similar between without control those an objective response. Growth baseline best overall points (BOR) that FGF-19 significantly increased ANG2 decreased at BOR. BOR point VEGF-D compared Summarily, ANG-2 might contribute developing be target molecules salvage therapies.

Language: Английский

Citations

11