Abstract 726P
Background
The combination of systemic therapies and hepatic arterial infusion chemotherapy (HAIC) showed promising outcomes for advanced hepatocellular carcinoma (HCC). Raltitrexed, an antimetabolic drug with long plasma concentrations half-life, could be used in short infusions. HAIC with raltitrexed plus oxaliplatin (RALOX) was reported to be effective and safe in HCC. This study aimed to investigated the efficacy and safety of combined camrelizumab and lenvatinib plus RALOX-HAIC as a first-line treatment in advanced HCC patients.
Methods
This single-arm, phase II study included treatment-naive adult (≥18 years) patients with HCC in BCLC stage B and C and Child-Pugh score small or equal to 7 points (NCT05003700). Patients were administrated with RALOX-HAIC (oxaliplatin 100mg/m2, raltitrexed 3 mg/m2, every 3 weeks), combined with camrelizumab (200mg by IV infusion, every 3 weeks) and lenvatinib (8mg orally once daily) for 6 cycles, followed by maintenance therapy with camrelizumab and lenvatinib until disease progression or unacceptable toxicity. The primary endpoint was objective response rate (ORR).
Results
Between March 2021 and February 2022, 26 patients (23 men and 3 women; median age, 53.5 years) were enrolled. The median tumor size was 11.3 cm, 88.5% of patients had portal vein invasion, and 23% had extrahepatic metastasis. As of April 20, 2022, the median follow-up was 8.4 months, and all patients had at least one post-baseline tumor assessment. The confirmed ORR per RECIST v1.1 and mRECIST was respectively 57.7% (95% CI, 37.3-78.0), and 80.8% (95% CI, 64.5-97.0) including 2 (7.7%) patients who achieved a complete radiological response. Grade 3-4 treatment-related adverse events (AEs) occurred in 61.5% of patients, and the most common were thrombocytopenia (23.1%), elevated aspartate aminotransferase (23.1%), leucopenia (15.4%) and abdominal pain (15.4%). All AEs were expected and manageable, and no treatment-related deaths were reported.
Conclusions
Combination treatment with camrelizumab and lenvatinib plus RALOX-HAIC showed promising antitumor activity and acceptable toxicity in patients with advanced HCC.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
GuangDong Basic and Applied Basic Research Foundation (2020A1515110941); The Natural Science Foundation of Guangdong Province (2021A1515012518, and 2022A1515010526); The National Natural Science Foundation of China (82102879).
Disclosure
All authors have declared no conflicts of interest.