Unknown

Dataset Information

0

Significance of post-progression therapy after tyrosine kinase inhibitors for advanced hepatocellular carcinoma.


ABSTRACT:

Background and aim

Molecular-targeted therapies such as sorafenib and lenvatinib have long been used as first-line treatment for advanced hepatocellular carcinoma (aHCC). However, adverse events or limited therapeutic effects may necessitate the change to another therapeutic option, known as post-progression therapy. To investigate the significance of post-progression therapy, we analyzed the outcomes of aHCC patients following first-line molecular-targeted therapy in a real-world study.

Methods

This retrospective, multicenter study involved patients with aHCC who received sorafenib or lenvatinib as first-line therapy between January 2011 and September 2021.

Results

In total, 513 patients were analyzed: 309 treated with sorafenib and 204 with lenvatinib. The overall response and disease control rates were 15 and 50%, respectively, in the sorafenib group and 30 and 75%, respectively, in the lenvatinib group (P < 0.001). Kaplan-Meier analysis revealed no significant differences in progression-free survival and overall survival (OS) between the two treatments. Multivariate analysis revealed that fibrosis-4 index, disease control rate, post-progression therapy, and use of an immune checkpoint inhibitor (ICI) were significantly associated with OS. OS was significantly longer in patients who received post-progression therapy than in those who did not (log-rank P < 0.001). Most patients who received an ICI as post-progression therapy had previously received lenvatinib. Among lenvatinib-treated patients, OS was significantly longer in patients who received an ICI than in patients received another or no post-progression therapy (P = 0.004).

Conclusion

The introduction of newer drugs for post-progression therapy is expected to prolong survival. ICI-based regimens appear to be effective after lenvatinib.

SUBMITTER: Yano Y 

PROVIDER: S-EPMC9218537 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC3356077 | biostudies-literature
| S-EPMC7732574 | biostudies-literature
| S-EPMC8543014 | biostudies-literature
| S-EPMC3210627 | biostudies-literature
| S-EPMC3328820 | biostudies-literature
| S-EPMC7098670 | biostudies-literature