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.
Resources from the same session
341P - NUP214 gene rearrangements in leukemia patients: Case series from a single institution
Presenter: Yu Jeong Choi
Session: Poster Display
Resources:
Abstract
344P - Venetoclax and azacitidine compared with azacitidine monotherapy for acute myeloid leukemia patients: A systematic review and meta-analysis
Presenter: Azzahra Noersamsjah
Session: Poster Display
Resources:
Abstract
345P - Safety and efficacy of platinum substitution in induction chemotherapy for mantle cell lymphoma
Presenter: Omali Pitiyarachchi
Session: Poster Display
Resources:
Abstract
346P - An assessment of marrow-infiltrating T cells in early relapsed hematologic cancer patients after allogeneic hematopoietic stem cell transplantation
Presenter: Ik-Chan Song
Session: Poster Display
Resources:
Abstract
347P - New targets for adult T cell leukemia/lymphoma (ATLL): A map for ATLL immunotherapy
Presenter: Zahra Rezaei Borojerdi
Session: Poster Display
Resources:
Abstract
348P - In-depth molecular analysis in the diagnosis of lymphomas with lymphoplasmacytic differentiation may provide a more precise diagnosis and rational treatment allocation
Presenter: Ella Willenbacher
Session: Poster Display
Resources:
Abstract
349P - Overall survival and progression-free survival comparison of lenalidomide + standard therapy versus standard therapy only in indolent lymphoma: A meta-analysis
Presenter: Kevin Winston
Session: Poster Display
Resources:
Abstract
350P - Intratumoural CD66b+ to predict treatment response in diffuse large B cell lymphoma (DLBCL)
Presenter: Mita Adriani
Session: Poster Display
Resources:
Abstract
351P - Clinical features and treatment outcomes of Waldenstrom macroglobulinemia patients: A single center study
Presenter: Devi Amelia
Session: Poster Display
Resources:
Abstract
352TiP - Randomized phase III study of daratumumab (D) versus bortezomib plus D as a maintenance therapy after D-MPB for elderly or non-elderly patients refusing transplant with untreated multiple myeloma (JCOG1911, B-DASH study)
Presenter: Tomotaka Suzuki
Session: Poster Display
Resources:
Abstract