Abstract 976P
Background
First-line systemic therapy (ST) options in advanced hepatocellular carcinoma (HCC) include tyrosine kinase inhibitors and immunotherapy (IO). Evolving data suggest prolonged overall survival (OS) when ST approaches are combined with stereotactic radiation therapy (SRT), although evidence is limited in HCC populations. We hypothesized that advanced HCC patients in the United States National Cancer Database (NCDB) would have improved OS when receiving ST+SRT vs ST alone.
Methods
Stage III/IV HCC patients diagnosed from 2010-2020 and treated with first-line ST±SRT were identified from the NCDB. The primary endpoint was OS from date of diagnosis stratified by the receipt of SRT (ST+SRT vs ST alone). Survival was estimated using Kaplan-Meier methodology and compared via log-rank. Multivariate analysis (MVA) was performed by Cox regression.
Results
Of 10,505 eligible patients with stage III disease, 115 (1.1%) received ST+SRT and 10,390 (98.9%) received ST alone. Of 9,617 eligible patients with stage IV disease, 127 (1.3%) received ST+SRT and 9,490 (98.6%) received ST alone. Median follow-up time was 6.8 months. Baseline characteristics were similar between cohorts. Patients with stage III disease receiving ST+SRT had improved median OS (12.62 months vs. 8.38, log-rank P=0.0054) and higher rates of survival at 1-year (53.0% vs. 38.7%) and 2-years (27.0% vs. 20.7%) compared to those receiving ST alone. Similarly, patients with stage IV disease receiving ST+SRT had improved median OS (11.79 months vs 5.72 months, log-rank P<0.0001) and higher rates of survival at 1-year (49.6% vs 26.2%) and 2-years (23.6% vs. 12.0%). On MVA, receipt of SRT predicted for improved OS (HR=0.748, P=0.0178) and receipt of IO trended towards improved OS (HR=0.859, P=0.0538). Predictors of poor OS included stage IV disease (HR=1.509), primary tumor size > 5 cm (HR=1.354), and Charlson-Deyo Score >0 (HR=1.106) (P=<0.0001).
Conclusions
In patients with stage III/IV HCC, concomitant ST+SRT improved OS compared to ST alone. Prospective clinical trials are warranted to better identify HCC populations which may benefit from combined modality therapy.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Saint Louis University.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
967P - The effect of prognosis value of EZH2 (Enhancer Of Zeste Homologue) staining in hepatocellular cancer
Presenter: Mehmet Kidi
Session: Poster session 18
968P - High sensitivity routine blood based detection of HCC: An AI model from 220k patients
Presenter: Kin Nam Kwok
Session: Poster session 18
969P - Establishing a novel routine blood component signature for Hepatocellular Carcinoma (HCC) screening with big clinical data
Presenter: Ka Man Cheung
Session: Poster session 18
970P - Real-world multi-center study of systemic treatment after first-line atezolizumab plus bevacizumab for advanced hepatocellular carcinoma in Asia-Pacific countries
Presenter: Choong-kun Lee
Session: Poster session 18
971P - Effect of preoperative frailty on surgical outcomes following hepatic resection for elderly patients with hepatocellular carcinoma: A multicenter retrospective cohort study from China
Presenter: Zhongqi Fan
Session: Poster session 18
972P - Sequential therapies after atezolizumab plus bevacizumab or lenvatinib first-line treatments in advanced hepatocellular carcinoma
Presenter: Mara Persano
Session: Poster session 18
973P - Clinicopathologic and treatment outcome data in 165 fibrolamellar carcinoma patients
Presenter: Sunyoung Lee
Session: Poster session 18
974P - The barthel index predicts surgical textbook outcomes following hepatectomy for elderly patients with hepatocellular carcinoma: A multicenter cohort study from China
Presenter: Guoyue Lv
Session: Poster session 18
975P - The clinical impact of urinary protein creatinine ratio and AFP at six weeks in patients with unresectable hepatocellular carcinoma treated with atezolizumab plus bevacizumab
Presenter: Kaoru Tsuchiya
Session: Poster session 18