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
956P - Phase II study of adjuvant tislelizumab combined with interferon-α and active surveillance in hepatocellular carcinoma patients with microvascular invasion
Presenter: Yixiu Wang
Session: Poster session 18
957P - Interim report of Notable-HCC: A phase Ib study of neoadjuvant PD-1 with stereotactic body radiotherapy in patients with resectable hepatocellular carcinoma (HCC)
Presenter: Mingming Li
Session: Poster session 18
959P - Combination therapy of envafolimab and suvemcitug in patients with hepatocellular carcinoma (HCC): Results from a phase II clinical trial
Presenter: Lixia Ma
Session: Poster session 18
960P - Personalized circulating tumor DNA (ctDNA) monitoring for recurrence detection and treatment response assessment in hepatocellular carcinoma (HCC)
Presenter: Maen Abdelrahim
Session: Poster session 18
961P - Blood circulating Galectin-3 is a prognostic biomarker in hepatocellular carcinoma
Presenter: Shadi Chamseddine
Session: Poster session 18
962P - SBRT improves the efficacy of immuno-checkpoint inhibitors for hepatocellular carcinoma through the activation of IL-6/JAK1-STAT3/PD-L1 axis mediated by MBD3 degradation
Presenter: Weiwei Yan
Session: Poster session 18
963P - Discovery and validation of cfDNA methylation, AFP and ctDNA mutation for the early detection of hepatocellular carcinoma: A multicenter prospective study (ASCEND-Hep)
Presenter: Mingxin Pan
Session: Poster session 18
966P - Potential role of neuropilin-1 in the prognosis, development and risk of invasion in hepatocellular carcinoma patients
Presenter: Tania Payo-Serafín
Session: Poster session 18