Abstract 973P
Background
Atezolizumab plus bevacizumab (A+B) and lenvatinib (L) are approved first line systemic therapies for advanced hepatocellular carcinoma (HCC). They demonstrated superiority to sorafenib in clinical trials, but assessment from big real world data (RWD) studies are lacking. Here we present results of overall survival (OS) using the TrinetX platform.
Methods
Using TriNetX Global Collaborative Network we identified patients with advanced HCC from 66 healthcare organizations treated with S, L or A+B as first line systemic therapy. Treatment start happend between January 2015 and December 2022. Propensity score (PSM) was used to balance cohorts on age, gender and race. Kaplan-Meier analysis was used to compare the 5-year overall survival (OS) between the cohorts.
Results
We identified 7038 patients: 1030 treated with A+B, 1674 with L, and 4334 with S. Mean age was 65 years old and 78% were male. Second line therapy was received by 1682 patients (23.8%), 48% of them with immunotherapy. When analysing raw data, OS was significantly better with A+B (mOS 449 days) compared to S (mOS 374 days) (HR 0.88, 95% CI 0.80-0.97, p=0.047), and with L (mOS 460 days) compared to S (HR 0.90, 95% CI 0.84-0.98). After matching cohorts by sex, age, and race OS difference maintained with A+B vs S (HR 0.83, 95% CI 0.73-0.93, p=0.002) but it was not significant for L vs S (HR 0.92, 95% CI 0.84-1.01, p=0.12).
Conclusions
In this RWD setting, A+B maintains a robust OS benefit when compared to S as first line therapy for advanced HCC. L seems to be superior to S but difference in OS is not significant when patients data are matched. These results support the use of A+B as standard treatment.
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
1156P - The efficacy of lower doses of everolimus in patients with advanced neuroendocrine tumors
Presenter: Rachel Riechelmann
Session: Poster session 17
1157P - Retreatment with peptide receptor radionuclide therapy (PRRT) in patients (p) with neuroendocrine tumors (NET): Spanish clinical experience from SEPTRALU national registry
Presenter: Jorge Hernando Cubero
Session: Poster session 17
1158P - A novel nomogram for predicting overall survival of small intestinal neuroendocrine tumors treated with PRRT
Presenter: Dimitrios Papantoniou
Session: Poster session 17
1159P - Molecular characterization of extra-pulmonary mixed adeno-neuroendocrine carcinomas: The NIRVANA substudy
Presenter: Francesca Spada
Session: Poster session 17
1160P - An Italian multicenter phase II trial of metronomic temozolomide in unfit patients with advanced neuroendocrine neoplasms: Interim analysis of the MeTe study
Presenter: Francesca Spada
Session: Poster session 17
1161P - Progression-free survival ratio and the implications for treatment sequencing in neuroendocrine neoplasms
Presenter: Philipp Melhorn
Session: Poster session 17
1162P - Transcriptomic analysis of gastroenteropancreatic neuroendocrine tumours with carcinoid syndrome
Presenter: Javier Pozas Perez
Session: Poster session 17
1163P - Prognostic value of systemic inflammatory index (SII) in neuroendocrine tumors (NETs) treated with peptide receptor radionuclide therapy (PRRT)
Presenter: Eduardo Terán Brage
Session: Poster session 17
1164P - The influence of neoadjuvant radiotherapy on surgical management and prognostic outcomes in locally advanced rectal neuroendocrine carcinoma
Presenter: Weiran Xu
Session: Poster session 17