Abstract 91P
Background
Data on elucidating the efficacy and safety of tislelizumab combined with tyrosine kinase inhibitors (TKIs) in hepatocellular carcinoma (HCC) are lacking. Herein, we explored the regimen of tislelizumab plus TKIs for intermediate or advanced HCC patients (pts) in a real-world setting.
Methods
In this study, 73 pts were included between Jul. 2021 and Jul. 2023. Pts were assigned either with tislelizumab plus TKIs (n=33), or tislelizumab plus TKIs plus TACE (n=40), where TKIs included lenvatinib (49.3%), regorafenib (23.3%), donafenib (21.9%), apatinib (2.7%) and anlotinib (2.7%). The primary endpoints were objective response rate (ORR, mRECIST criteria) and progression-free survival (PFS). The secondary endpoints included 6-month and 12-month PFS rates, disease control rate (DCR) and safety.
Results
Among the 73 pts, 80.8% were male, 53.4% had BCLC stage B, 75.3% were Child-Pugh A, 69.9% were first-line recipients and the average age was 62.8 years. The mean follow-up period was 13.3 (95% CI: 11.9-14.8) months and the mean number of TACE sessions were 0.8 (range 0-3) for all patients. The ORR and DCR were 42.5% and 79.5% with a median PFS of 12.6 months (95% CI: 8.71-16.49) and the 6-month, 12-month PFS rates were 69.6% and 50.4%. Compared to the tislelizumab plus TKIs group, the tislelizumab plus TKIs plus TACE group achieved longer median PFS (12.7 months (95% CI 9.17-16.23) vs. 8.4 months (95% CI 4.83-11.97), P=0.132), higher ORR (55.0% vs 27.3%, P = 0.017) and DCR (87.5% vs 69.7%, P = 0.061). Any-grade TRAEs were reported in 59 (80.8%) pts, and grade 3 TRAEs were reported in 16 (21.9%) pts. Most frequent TEAEs (≥10%) included hand-foot syndrome (24.7%), increased transaminase (15.1%), hyperbilirubinemia (13.7%), diarrhea (13.7%) and fever (11.0%). G3 TRAEs occurred in more 5% pts included hand-foot syndrome (8.2%), increased transaminase (6.8%). No grade 4/5 TRAE and new safety signal were identified.
Conclusions
Tislelizumab plus TKIs with TACE appeared to deliver encouraging efficacy and acceptable safety for pts with intermediate or advanced HCC. Further patient recruitment and longer follow up are warranted.
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
137P - First-in-human results from a Phase I dose-escalation study of VSV-GP (BI 1831169) in patients with advanced solid tumors
Presenter: Stephane Champiat
Session: Poster Display
138P - Generation of frameshift mutated TGF_R2-specific T cells in healthy subjects following administration with cancer vaccine candidate FMPV-1/GM-CSF
Presenter: Else Inderberg
Session: Poster Display
139P - Safety and clinical activity of a novel anti-CCR8 antibody (LM-108) as a single agent or in combination with pembrolizumab in patients with advanced solid tumors: Results of phase 1 study
Presenter: Alexander Starodub
Session: Poster Display
140P - Eliciting mAbs targeting MHC-bound peptides with a novel antibody discovery platform
Presenter: Elli Sandberg
Session: Poster Display
141P - An IgE antibody targeting the melanoma-associated Chondroitin Sulfate Proteoglycan 4
Presenter: Lais Cristina Palhares
Session: Poster Display
142P - Identifying novel immunotherapy targets using machine learning and ex vivo validation
Presenter: Marcellus Augustine
Session: Poster Display
143P - Advancing Cancer Immunotherapy via HLA-G Pathway Modulation with UCB4594
Presenter: Ann WHITE
Session: Poster Display
144P - Discovery of CBO421, a first-in-class Drug Fc-Conjugate (DFC), targeting CD73 in Cancer
Presenter: Simon Döhrmann
Session: Poster Display
145P - An Engineered Ligand-Trap Biologic Targeting the CD47 Signaling Pathway for Cancer Treatment with Superb Efficacy and Safety Profiles
Presenter: ZONG SEAN JUO
Session: Poster Display
146P - A Novel Allosteric Oral Immunotherapy Small Molecule Modulates Adenosine 2A Receptor Signaling and Restores Anti-Tumor Immune Responses
Presenter: David Pejoski
Session: Poster Display