Published online Jun 28, 2023. doi: 10.3748/wjg.v29.i24.3871
Peer-review started: March 26, 2023
First decision: April 26, 2023
Revised: May 6, 2023
Accepted: May 30, 2023
Article in press: May 30, 2023
Published online: June 28, 2023
Processing time: 94 Days and 9.2 Hours
Hepatocellular carcinoma (HCC) accounts for the third-leading cause of cancer-related deaths, and only 30%-40% of patients were diagnosed at early stages. The oligometastatic HCC indicated the metastasis of HCC was not widespread, and some patients may obtain benefits for curative treatments.
Stereotactic body radiotherapy (SBRT) and programmed cell death 1 (PD-1) inhibitors are widely used for HCC, whether the use of SBRT combined with a PD-1 inhibitor could offer superior benefits for oligometastatic HCC remained unclear.
To assess the efficacy and safety of combining SBRT with sintilimab for patients with recurrent or oligometastatic HCC.
Patients with recurrent or oligometastatic HCC were involved and treated with combining SBRT with sintilimab for 12 mo or disease progression. The primary endpoint was progression-free survival (PFS), while the secondary endpoints included overall survival (OS), local control rate, objective response rate (ORR), disease control rate (DCR), and adverse events.
The median PFS was 19.7 mo [95% confidence interval (CI): 16.9-NA], while the median OS was not reached. Moreover, the 1- and 2-year local control rate were 100% and 90.9% (95%CI: 75.4%-100.0%), while the ORR and DCR were 96%, and 96%, respectively. Only 3 patients reported grade 3 adverse events, including increased gamma-glutamyl transpeptidase level, decreased platelet count, and myositis.
SBRT plus sintilimab can serve as an effective, well-tolerated treatment regimen for patients with recurrent or oligometastatic HCC.
Further large-scale, parallel-control randomized controlled trials should be performed to verify the therapeutic effects of SBRT plus sintilimab for patients with recurrent or oligometastatic HCC.