Abstract 968P
Background
The LEAP-002 trial showed Lenvatinib plus Pembrolizumab (a programmed death-1 [PD-1] inhibitor) was more beneficial to patients with hepatocellular carcinoma (HCC) and macrovascular invasion compared to Lenvatinib alone. Recently, hepatic arterial infusion chemotherapy (HAIC) has shown promising results for advanced HCC with portal vein tumor thrombosis (PVTT). This trial was to compare the efficacy and safety of HAIC combined with Lenvatinib and PD-1 inhibitors to Lenvatinib plus PD-1 inhibitors for patients with advanced HCC and PVTT.
Methods
Participants with advanced HCC and PVTT were enrolled and assigned 1:1 to HAIC + Lenvatinib + PD-1 inhibitor group (Lenva-PD1-HAIC group) or Lenvatinib + PD-1 inhibitor group (Lenva-PD1 group). HAIC was performed via a percutaneously implanted port-catheter system with 3cir-OFF regimen (oxaliplatin [35 mg/m2, 0-2h, d1-3] and 5-fluorouracil [600 mg/m2, 2-24h, d1-3], repeated every 4 weeks). Lenvatinib was administered orally (12 mg/d [≥ 60 kg] or 8 mg/d [< 60 kg]), and PD-1 inhibitors were administered intravenously on day 1 every 3-4 weeks. Six-month progression-free survival (PFS) rate, overall survival (OS), PFS, objective response rate (ORR) (mRECIST criteria), time to progression (TTP), and safety were compared.
Results
From December 2021 to December 2023, 66 participants were enrolled with 33 in each group. The 6-month PFS rate was 78.8% vs. 46% (p = 0.011). The median PFS was 12.3 vs. 5.9 months (p = 0.001), and the median TTP was 12.3 vs. 5.3 months (p = 0.002). The median OS was not reached vs. 15.7 months, with the 1- and 2-year OS rate of 73.8% vs. 60% and 61.6% vs. 30.5%, respectively. The ORR was 75.8% vs. 37.5% (mRECIST criteria) (p = 0.006). The incidence of Grade 3-4 treatment-related adverse events (AEs) was 51.5% vs. 30.3%. Elevated AST (6/33, 18.2%)was the most frequent Grade 3-4 AEs in Lenva-PD1-HAIC group, while hypertension (6/33, 18.2%) was the most frequent Grade 3-4 AEs in Lenva-PD1 group.
Conclusions
HAIC combined with Lenvatinib and PD-1 inhibitors showed greater efficacy and acceptable safety profile for advanced HCC with PVTT compared to Lenvatinib plus PD-1 inhibitors.
Clinical trial identification
NCT05166239; Release date: 11/26/2021.
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
National Natural Science Foundation of China (No. 82172039), Beijing Hospitals Authority Clinical Medicine Development of Special Funding Support (No. ZYLX202117), and Beijing Natural Science Foundation (No. 7212198).
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1427P - Predicting overall survival and prognostic indicator genes in esophagogastric cancer patients using machine learning and bioinformatics analysis
Presenter: Nguyen-Kieu Viet-Nhi
Session: Poster session 17
1428P - Total neoadjuvant FLOT chemotherapy in oesophagogastric adenocarcinoma: An international cohort study
Presenter: Hollie Clements
Session: Poster session 17
1429P - Differences in esophageal cancer incidence and survival by race/ethnicity: A SEER analysis
Presenter: Ashwin Kulshrestha
Session: Poster session 17
1430P - Impact of menadione supplementation in the treatment of patients with metastatic gastric cancer: A randomized phase II clinical trial
Presenter: Francisco Cezar Moraes
Session: Poster session 17
1431P - Assessing pathological complete response to neoadjuvant chemotherapy combined with immunotherapy in esophageal squamous cell carcinoma: A deep learning approach with voxel-level radiomics
Presenter: Yongling Ji
Session: Poster session 17
1432P - Safety of laparoscopic D2 distal gastrectomy following neoadjuvant chemotherapy for locally advanced gastric cancer patients: A prospective multicenter trial (CLASS-03a)
Presenter: Kun Yang
Session: Poster session 17