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Poster Display session

184P - Lenvatinib (L) versus sorafenib (S) second-line therapy in hepatocellular carcinoma (HCC) patients (P) progressed to atezolizumab plus bevacizumab (AB)

Date

27 Jun 2024

Session

Poster Display session

Presenters

Silvia Camera

Citation

Annals of Oncology (2024) 35 (suppl_1): S75-S93. 10.1016/annonc/annonc1478

Authors

M. PERSANO1, M. Rimini2, S. Foti3, S. Camera3, F. Rossari4, E. Amadeo2, F. Vitiello2, T. Tada5, G. Suda6, S. Shimose7, M. Kudo8, C. Yoo9, J. Cheon10, F. Finkelmeier11, H.Y. Lim12, J. Presa13, L. Mascia14, S. Cascinu2, M. Scartozzi15, A. Casadei Gardini2

Author affiliations

  • 1 AOU di Cagliari - Ospedale Civile, Cagliari/IT
  • 2 IRCCS Ospedale San Raffaele, Milan/IT
  • 3 Vita-Salute San Raffaele University, IRCCS San Raffaele Scientific Institute Hospital, Milan/IT
  • 4 IRCCS Ospedale San Raffaele, 20132 - Milan/IT
  • 5 Japanese Red Cross Society Himeji Hospital, Himeji/JP
  • 6 Hokkaido University Hospital, Sapporo/JP
  • 7 Kurume University Hospital, Kurume/JP
  • 8 Kindai University Faculty of Medicine, Osaka/JP
  • 9 Asan Medical Center - University of Ulsan, Seoul/KR
  • 10 Ulsan University Hospital, Ulsan/KR
  • 11 Goethe-University Frankfurt am Main - Campus Westend, Frankfurt am Main/DE
  • 12 Samsung Medical Center (SMC) - Sungkyunkwan University School of Medicine, Seoul/KR
  • 13 rás-os-Montes e Alto Douro Hospital Centre, Vila real/PT
  • 14 A. Businco Cancer Center, A. R. N. A. S. Brotzu, Cagliari/IT
  • 15 University Hospital and University of Cagliari, 9042 - Monserrato/IT

Resources

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Abstract 184P

Background

This retrospective multicenter real-world study aims to compare outcomes reached by L and S second-line therapy in HCC P treated with first-line AB.

Methods

The overall cohort included 891 HCC P from 5 countries (Italy, Germany, Portugal, Japan, and the Republic of Korea) treated with AB in first-line setting. 53.0% of P had progressive disease after first-line therapy, of which 51.5% received a second-line treatment. Data from 137 P were available: 37.2% received S and 62.8% L.

Results

L second-line subgroup achieved a median overall survival (mOS) of 18.9 months (mo), significative longer (p = 0.01; HR: 2.24) compared to S subgroup that reached a mOS of 14.3 mo. After adjusting for positive clinical covariates at univariate analysis, multivariate analysis highlighted ALBI 1 grade [p < 0.01; hazard ratio (HR): 5.23] and L second-line therapy (p = 0.01; HR: 2.18) as positive prognostic factor for OS. Forest plot highlighted a positive trend in terms of OS in favor of P treated with L second-line regardless of baseline characteristics before first-line therapy. In particular, L second-line subgroup had a better OS compared to S second-line subgroup in male P, aged ≤ 70 years, with viral etiology, BCLC C stage, αfetoprotein < 400 ng/mL, Child-Pugh A, NLR < 3, ALBI 1 grade, performance status ≤ 1, presence of portal vein thrombosis. Regarding first-line outcomes, L second-line subgroup achieved a median progression-free survival (mPFS) of 3.5 mo, while S second-line subgroup reached a mPFS of 4.3 mo without any significative difference (p 0.42; HR: 1.15). There was no difference in overall response rate (L 26.1% vs. S 19.8%; p = 0.29) and disease control rate (L 76.8% vs. S 66.4%; p = 0.71) between the two subgroups. Among the group of P reaching a first-line PFS inferior to 6.0 mo, P treated with L second-line achieved a mOS of 17.0 mo significative longer (p = 0.02; HR: 2.24) compared to those treated with S second-line (9.2 mo). Within the group of P reaching a first-line PFS superior to 6.0 mo, there was no difference in mOS between the two subgroups (S 15.7 mo vs. L not reached; p = 0.12; HR: 2.41).

Conclusions

L second-line therapy is superior to S in HCC P progressed to first-line AB.

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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