Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster Display session

185P - The combined role of patients (pts) gender and disease etiology on unresectable HCC (uHCC) first-line (1L) treatment outcome

Date

27 Jun 2024

Session

Poster Display session

Presenters

Silvia Cesario

Citation

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

Authors

S. Cesario1, V. Genovesi2, M. Rimini3, T. Tada4, G. Suda5, S. Shimose6, M. Kudo7, F. Finkelmeier8, C. Yoo9, J. Presa10, M.A. Iavarone11, F. Marra12, F.G. Foschi13, E. Tamburini14, S. Lonardi15, F. Piscaglia16, F. Salani2, C. Vivaldi17, A. Casadei Gardini3, G. Masi18

Author affiliations

  • 1 AOU Pisana - Stabilimento di Santa Chiara, Pisa/IT
  • 2 Azienda Ospedaliera Universitaria Pisana, Pisa/IT
  • 3 IRCCS Ospedale San Raffaele, Milan/IT
  • 4 Japanese Red Cross Society Himeji Hospital, Himeji/JP
  • 5 Hokkaido University Hospital, Sapporo/JP
  • 6 Kurume University Hospital, Kurume/JP
  • 7 Kindai University Faculty of Medicine, Osaka/JP
  • 8 Goethe-University Frankfurt am Main - Campus Westend, Frankfurt am Main/DE
  • 9 Asan Medical Center - University of Ulsan, Seoul/KR
  • 10 rás-os-Montes e Alto Douro Hospital Centre, Vila real/PT
  • 11 Ospedale Maggiore Policlinico - Fondazione IRCCS Ca' Granda, Milan/IT
  • 12 UniFI - Università degli Studi di Firenze, Firenze/IT
  • 13 Ospedale di Faenza, Faenza/IT
  • 14 Azienda Ospedaliera Cardinale Giovanni Panico, Tricase/IT
  • 15 IOV - Istituto Oncologico Veneto IRCCS, Padova/IT
  • 16 AOU Policlinico S. Orsola-Malpighi, Bologna/IT
  • 17 Azienda Ospedaliero Universitaria Pisana - Stabilimento di Santa Chiara, Pisa/IT
  • 18 Unit of Medical Oncology 2, Azienda Ospedaliera Universitaria Pisana, Pisa/IT

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 185P

Background

The role of pts gender and disease etiology on 1L treatment outcome in uHCC is still debated. We investigated the putative prognostic effect of these factors on real-world uHCC overall survival (OS) and progression-free survival (PFS) on atezolizumab/bevacizumab (AB) or lenvatinib (L) 1L.

Methods

We conducted a retrospective multi-center, multi-National (Europe and Asiatic non-China), analysis of well-characterized uHCC pts receiving AB or L. Univariate analyses for OS and PFS were conducted after stratifying pts as viral males (VM), non-viral males (NVM), viral females (VF), and non-viral females (NVF) with the Kaplan-Meier method. Cox regression was used to adjust for patients’ subgroup imbalances.

Results

We included 1,759 male and 467 female pts. One hundred fifty-four (60%) male pts received L and 705 (40%) AB. VM were 56%. Significantly (p<0.05) different characteristics of NVM vs VM were higher age at diagnosis, less frequent prior locoregional therapies (LRT), higher Child Pugh score, and lower alfafetoprotein (AFP). Female pts received L in 287 cases (62%) and AB in 180 (38%). VF were 60%. Significantly (p<0.05) different characteristics of NVF vs VF included less frequent prior LRT and higher AFP. At a median follow-up of 12.7 months, no differences in terms of OS were found for gender with either L (HR 1.05, p 0.61) or the AB treatment (HR 1.17, p 0.30). In male pts, PFS was prolonged with AB compared to L (HR, 0.83 p 0.002). In VM, no statistical difference in terms of OS was identified between the two treatments, whilst AB improved PFS over L (HR 0.76, p 0.001). AB superiority in PFS was not confirmed in NVM. In female pts, no difference between the two treatments in terms of OS (HR 1.04, p 0.78) and PFS (HR 0.81, p 0.10) was identified. In VF, AB improved PFS compared to L (HR 0.72, p 0.049); in NVF no differences were observed. In the exploratory analysis of BCLC-B pts, L improved OS over AB only in NVF (p 0.030). After adjusting for differential clinical factors, the independent role in PFS for AB was confirmed only in VM (p=0.0002).

Conclusions

This analysis revealed no significant differences in OS for either AB or L when selecting pts by gender and etiology. In VM, AB is an independent factor of improved PFS.

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.