AI Article Synopsis

  • A study was conducted to compare the effectiveness and safety of three treatment options for unresectable recurrent hepatocellular carcinoma (HCC): transarterial chemoembolization combined with lenvatinib and PD-1 inhibitors (T-L-P), TACE with lenvatinib (T-L), and TACE alone.
  • Among 204 patients analyzed, those in the T-L-P group had the best survival outcomes and disease control rates compared to the other two groups.
  • The study concluded that the T-L-P regimen is both safe and significantly better in enhancing survival for patients dealing with unresectable recurrent HCC.

Article Abstract

Background: There is no consensus on the optimal regimen for unresectable recurrent hepatocellular carcinoma (HCC), so this retrospective study aimed to evaluate the efficacy and safety of transarterial chemoembolization (TACE) combined with lenvatinib and PD-1 inhibitors (T-L-P) versus TACE combined with lenvatinib (T-L) or TACE alone.

Method: Data were collected from 204 patients with unresectable recurrent HCC who received T-L-P, T-L, or TACE alone at three medical centers from January, 2019 to December, 2020 for analysis. The survival outcomes, tumor response, and adverse events were compared between three groups, and risk factors were further investigated.

Results: The median overall survival in the T-L-P, T-L, and TACE alone groups were not reached, 25.6, and 15.7 months, respectively (p < 0.001). The median progression-free survival in the T-L-P, T-L, and TACE alone groups were 24.1, 17.3, and 13.7 months, respectively (p < 0.001). The best objective response rate in the T-L-P, T-L, and TACE alone groups were 70.4%, 48.9%, and 42.5%, respectively. The best disease control rate in the T-L-P, T-L, and TACE alone groups were 100.0%, 97.8%, and 87.5%, respectively. There was no significant difference between the T-L-P and T-L groups for Grade 3/4 adverse events.

Conclusion: T-L-P regimen was safe and superior to T-L or TACE alone in improving survival for unresectable recurrent HCC patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242311PMC
http://dx.doi.org/10.1002/cam4.5880DOI Listing

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