Abstract 1009P
Background
Advanced hepatocellular carcinoma (HCC) is a highly lethal disease with limited treatment options. The use of first-line (1L) systemic therapies showcase improved overall survival and quality of life. This study aimed to compare the objective response rate (ORR) of various systemic therapies for advanced HCC in 1L setting using a network meta-analysis.
Methods
A systematic literature review (SLR) and network meta-analysis (NMA) of randomized controlled trials (RCTs) was conducted to assess the efficacy of 1L systemic therapies for advanced HCC. Multiple databases, including PubMed, Embase, and the Cochrane Library were searched for relevant studies. The primary outcome of interest was the ORR of each therapy compared to placebo. The results were obtained for both fixed and random-effect models to estimate each therapy's relative risk (RR) and 95% credible intervals (CrI).
Results
A total of 12 RCTs met the inclusion criteria. The combination therapy of sintilimab + IBI305 had the highest ORR, with an RR of 13.6 (95% CrI: 3.69, 55.67) using fixed-effect and RR of 14.13 (95% CrI: 0.82, 120.1) using random-effect models. SUCRA values ranged from 0.075 for placebo to 0.761 for sintilimab + IBI30. SUCRA rankings were generally better for combination therapies followed by mono-therapies and placebo.
Conclusions
The NMA revealed that the combination therapies had the highest ORR among the systemic therapies in the 1L setting. The SUCRA values confirmed the high probability of these treatments ranking higher in terms of ORR and can be used to support treatment decision-making in clinical practice.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
G. Kaur, B. Singh, S. Attri, A. Sharma, P. Rai, S. Pandey: Financial Interests, Personal, Full or part-time Employment: Pharmacoevidence.
Resources from the same session
832P - Characterisation of EXS73565: A potent and selective MALT1 inhibitor with low drug-drug interaction risk and potential in lymphoma
Presenter: Major Gooyit
Session: Poster session 18
833P - New targets for adult T cell leukemia/lymphoma (ATLL): A map for ATLL immunotherapy
Presenter: Zahra Rezaei Borojerdi
Session: Poster session 18
834P - Phase II clinical study of VR-CAP regimen for first-line treatment of marginal zone lymphoma
Presenter: Junfeng Chu
Session: Poster session 18
835P - A safe and effective immunochemotherapy with oral sobuzoxane and etoposide for untreated diffuse large B cell lymphoma patients aged 80 and over
Presenter: Kaname Miyashita
Session: Poster session 18
838P - Matching-adjusted indirect comparison (MAIC) of axicabtagene ciloleucel (axi-cel) and epcoritamab (epcor) in relapsed/refractory (R/R) large B cell lymphoma (LBCL) after at least two prior systemic therapies (3L+)
Presenter: Olalekan Oluwole
Session: Poster session 18
840P - Genomic landscape, immune characteristics and prognostic mutation signature of extranodal NK/T cell lymphoma, nasal type in China
Presenter: Yue Chai
Session: Poster session 18
841P - Ki67-revised risk index to risk-stratify patients with extra-nodal natural killer/T cell lymphoma
Presenter: Shuo Li
Session: Poster session 18