AI Article Synopsis

  • Notable-HCC (NCT05185531) is a phase 1b clinical trial assessing the safety and early effectiveness of combining PD-1 blockade with stereotactic body radiotherapy (SBRT) in patients with early-stage hepatocellular carcinoma (HCC).
  • Twenty patients received SBRT and the anti-PD-1 drug tislelizumab before surgery, with results showing treatment-related adverse events mostly mild, and no delays or complications in surgery.
  • The trial found a 63.2% objective tumor response rate (with some complete responses) and reported that this neoadjuvant therapy is safe and can effectively shrink tumors before surgery.

Article Abstract

Notable-HCC (NCT05185531) is a phase 1b trial, aiming to evaluate the safety and preliminary effectiveness of neoadjuvant PD-1 blockade plus stereotactic body radiotherapy (SBRT) in early-stage resectable hepatocellular carcinoma (HCC). Twenty patients with HCC of BCLC stage 0-A received 3 Gy SBRT and two cycles of tislelizumab, an anti-PD-1 monoclonal antibody before the curative HCC resection. Primary endpoints were the surgery delay, radiographic and pathological tumor response after the neoadjuvant therapy, safety and tolerability. During the neoadjuvant therapy, treatment-related adverse events (TRAEs) of grade 1-2 occurred in all 20 patients (100%), eight patients (40%) had grade 3 TRAEs, no grade 4 to 5 TRAE occurred, and all resolved without corticosteroids treatment. Per mRECIST, the objective response rate was 63.2% (12/19), with 3 complete response; the disease control rate was 100%. Two (10.5%) patients achieved complete pathological response. No surgery delay occurred. The neoadjuvant therapy did not increase the surgical difficulty or the incidence of complications. Secondary endpoints of disease-free survival and overall survival were not mature at the time of the analysis. Our pilot trial shows that neoadjuvant therapy with anti-PD-1 + SBRT is safe and promotes tumor responses in early-stage resectable HCC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11021407PMC
http://dx.doi.org/10.1038/s41467-024-47420-3DOI Listing

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