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

188P - Impact of metformin, statin, aspirin and insulin on the prognosis of unresectable HCC patients receiving first-line lenvatinib or atezolizumab plus bevacizumab

Date

02 Dec 2023

Session

Poster Display

Presenters

Margherita Rimini

Citation

Annals of Oncology (2023) 34 (suppl_4): S1520-S1555. 10.1016/annonc/annonc1379

Authors

M. Rimini1, E. Amadeo1, F. Vitiello2, S. Foti2, M. Persano3, T. Tada4, G. Suda5, S. Shimose6, M. Kudo7, J. Cheon8, F. Finkelmeier9, H.Y. Lim10, F. Piscaglia11, G. Masi12, C. Yoo13, S. Lonardi14, F. Rossari15, S. Camera16, A. Casadei Gardini17, J. Presa18

Author affiliations

  • 1 Medical Oncology, IRCCS Ospedale San Raffaele, 20132 - Milan/IT
  • 2 Oncology, IRCCS Ospedale San Raffaele, 20132 - Milan/IT
  • 3 Medical Oncology Department, AOU di Cagliari - Ospedale Civile, IT-09124 - Cagliari/IT
  • 4 Internal Medicine, Japanese Red Cross Society Himeji Hospital, Himeji/JP
  • 5 Oncology, Hokkaido University, 060-0812 - Sapporo/JP
  • 6 Medical Oncology Department, Kurume University Hospital, 830-0011 - Kurume/JP
  • 7 Department Of Gastroenterology And Hepatology, Kindai University - Faculty of Medicine, 589-8511 - Osaka/JP
  • 8 Division Of Hematology And Oncology, Ulsan University Hospital, 44033 - Ulsan/KR
  • 9 Medical Oncology Department, Universitätsklinikum Frankfurt (Johannes-Wolfgang Goethe-Universität), 60590 - Frankfurt am Main/DE
  • 10 Oncology, Samsung Medical Center (SMC) - Sungkyunkwan University School of Medicine, 135-710 - Seoul/KR
  • 11 Oncology, AOU Policlinico S. Orsola-Malpighi, 40138 - Bologna/IT
  • 12 Medical Oncology, OSPEDALE SANTA CHIARA, Pisa/IT
  • 13 Oncology Dept., Asan Medical Center - University of Ulsan College of Medicine, 138-931 - Seoul/KR
  • 14 Oncology Department, IOV - Istituto Oncologico Veneto IRCCS, 35128 - Padova/IT
  • 15 Department Of Medical Oncology/sr-tiget, UniSR - Università Vita e Salute San Raffaele Milano, 20132 - Milan/IT
  • 16 Dipartimento Di Oncologia Medica, IRCCS Ospedale San Raffaele, 20132 - Milan/IT
  • 17 Medical Oncology Department, IRCCS Ospedale San Raffaele, 20132 - Milan/IT
  • 18 Oncology, rás-os-Montes e Alto Douro Hospital Centre, Vila real/PT

Resources

Login to get immediate access to this content.

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

Abstract 188P

Background

Due to its complex pathophysiology, several comorbidities have to be taken in count in clinical decision-making process for hepatocellular carcinoma (HCC) patients. The aim of the present work was to investigate the potential prognostic role of metformin, aspirin, statins and insulin use in a cohort of advanced HCC patients who received Lenvatinib or atezolizumab plus bevacizumab as first- line treatment.

Methods

The population included HCC patients who received Atezolizumab plus Bevacizumab or Lenvatinib as first- line therapy. Univariate and multivariate analyses were performed by Cox proportional hazard to assess possible association between patients’ baseline characteristics and survival outcomes.

Results

730 patients with HCC were included in the analysis: 430 received Lenvatinib and 300 received Atezolizumab plus Bevacizumab. In both the treatment arms, no statistically differences in terms of OS and PFS were highlighted in patients who make chronic use of statin, aspirin or insulin compared to those who do not. In the Atezolizumab plus Bevacizumab arm, 50 (16.5%) patients were recorded to chronically use metformin. Patients in metformin group showed significantly shorter OS compared to patients in no-metformin group [respectively, 14.9 months (95% CI 6.4-16.3) vs. 19.7 (95% CI 16.0-30.4); HR 1.9 (95% CI 1.1-3.2) p = 0.0248], as confirmed in multivariate analysis (HR 1.9; 95% CI, 1.1-3.1; p=0.0163). Moreover, patients in metformin group had significantly shorter PFS compared to patients in no-metformin group [respectively, 4.5 months (95% CI 2.9-14.2) vs. 5.8 (95% CI 4.1-34.0); HR 1.6 (95% CI 1.0-2.6) p = 0.0212], as confirmed in multivariate analysis (HR 1.7; 95% CI, 1.1-2.7; p=0.0147).No statistically significant differences in terms of both OS and PFS were found between patients in metformin group and patients in no-metformin group in Lenvatinib arm.

Conclusions

The present study reports the first analysis focused on the role of metformin in a large double cohort of patients affected by advanced HCC who received Lenvatinib or Atezolizumab plus Bevacizumab, thus showing a negative prognostic role of metformin use in the Atezolizumab plus Bevacizumab group.

Clinical trial identification

Editorial acknowledgement

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.