Main Session
Sep 30
PQA 08 - Gastrointestinal Cancer, Nonmalignant Disease, Palliative Care

3442 - Proton Radiotherapy Alone vs. Combined with Immuno-Oncology Agents (Proton-IO) or Tyrosine Kinase Inhibitors (Proton-TKI) for Intermediate to Advanced-Stage Hepatocellular Carcinoma

02:30pm - 03:45pm PT
Hall F
Screen: 13
POSTER

Presenter(s)

Rodney Cheng-En Hsieh, MD, PhD - Chang Gung Memorial Hospital Linkou Branch, Taoyuan City, Taiwan

R. C. E. Hsieh1, P. Y. Chen2, C. H. Lin3, Y. C. Chang4, K. C. Tr?n5, and C. W. Lee6; 1Departments of Medical Imaging and Radiological Sciences, Radiation Oncology, and Cancer Genome Research Center, Chang Gung Memorial Hospital at Linkou and Chang Gung University, Taoyuan City, Taiwan, 2Department of Radiation Oncology, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan, 3MD Anderson Cancer Center, Houston, TX, 4Department of Radiation Oncology, Chang Gung Memorial Hospital, Keelung, Taiwan, 5Department of Radiation Oncology and Proton Therapy Center, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan, 6Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan, Taiwan

Purpose/Objective(s): We aim to compare the outcomes of proton radiotherapy alone versus its combination with immuno-oncology agents (Proton-IO) or tyrosine kinase inhibitors (Proton-TKI) for the treatment of intermediate to advanced-stage hepatocellular carcinoma (HCC).

Materials/Methods: This retrospective study reviewed the medical records of 137 patients with Barcelona Clinic Liver Cancer (BCLC) stage B (N = 43) or C (N = 94) HCC who received proton radiotherapy alone (N = 64), Proton-IO (N = 44), or Proton-TKI (N = 29) at Linkou Chang Gung Memorial Hospital between 2020 and 2023. The most common dose fractionation schedules included 72.6 Cobalt Gray Equivalent (CGE) in 22 fractions (N = 123) and 66 CGE in 10 fractions (N = 8). Atezolizumab-bevacizumab (N = 33) and pembrolizumab (N = 5) were the most frequently used immuno-oncology agents, while tyrosine kinase inhibitors included lenvatinib (N = 16) and sorafenib (N = 13). Tumor vascular thrombosis was observed in 85 (62%) patients. Pretreatment Child-Pugh class A and B were documented in 125 (91%) and 12 (9%) patients, respectively.

Results: After a median follow-up of 20 months, patients treated with Proton-IO had a significantly higher 2-year overall survival (OS) rate compared to those treated with Proton-TKI or proton radiotherapy alone (79.2% vs. 46.4% vs. 53.0%, P = 0.008). We observed significantly higher 2-year progression-free survival (PFS; 45.1% vs. 13.8% vs. 17.1%, P < 0.001) and distant metastasis-free survival (DMFS; 81.6% vs. 61.1% vs. 64.3%, P = 0.016) rates in the Proton-IO group, compared to those treated with Proton-TKI or proton radiotherapy alone. No significant differences were observed in 2-year local control rates among the treatment groups (Proton-IO vs. Proton-TKI vs. Proton radiotherapy alone: 93.9% vs. 86.8% vs. 80.7%, P = 0.216). Multivariate analysis identified the use of immuno-oncology agents as a significant predictor of superior OS (P = 0.010), PFS (P < 0.001), and DMFS (P = 0.005), whereas a tumor size >10 cm was significantly associated with lower PFS (P = 0.013) and DMFS (P = 0.042).

Conclusion: For intermediate to advanced-stage HCC, proton radiotherapy combined with immuno-oncology agents was associated with superior OS, PFS, and DMFS rates, compared with proton irradiation alone or in combination with tyrosine kinase inhibitors.