Efficacy and safety in unresectable hepatocellular carcinoma using atezolizumab plus bevacizumab in later-line: A retrospective analysis of real-world evidence.

Authors

null

Jiamin Cheng

Senior Department of Hepatology, the 5th Medical Center of the PLA General Hospital, Beijing, China

Jiamin Cheng , Bowen Chen , Xinfeng Zhang , Guodong Su , Caiyun Peng , Lin Zhou , Jin Lei , Yinyin Li , Yinying Lu

Organizations

Senior Department of Hepatology, the 5th Medical Center of the PLA General Hospital, Beijing, China, Peking University 302 Clinical Medical School, Beijing, China, The Fifth School of Clinical Medicine, Anhui Medical University, Hefei, China, Senior Department of Oncology, the 5th Medical Center of the PLA General Hospital, Beijing, China

Research Funding

No funding received
None.

Background: As far, no data has been published about later-line application of atezolizumab plus bevacizumab (T+A) in patients with unresectable hepatocellular carcinoma (uHCC). Methods: We retrospectively recruited uHCC patients who treated with later-line T+A. Efficacy endpoints included overall survival (OS) and progression free survival (PFS), in accordance with RECIST v1.1. Safety was evaluated with CTCAE v5.0. We also continually enrolled uHCC patients who received later-line regorafenib plus PD-1 inhibitors (Reg+PD-1) as a comparison. Results: Total 33 patients were continually included, 12 used T+A and 21 chose Reg+PD-1. Baseline performance status, liver function and BCLC tumor stage were similar between two cohorts. At data cut-off at February 2023, following median following-up at 18.9 months, median OS in cohort T+A and Reg+PD-1 were 8.2 (95%CI: 5.8-10.6) vs 15.6 (95%CI: 7.6-23.6) (p = 0.237). Median PFS in cohort T+A and Reg+PD-1were 5.1 (95%CI: 1.1-9.1) vs 3.5 (95%CI: 2.1-4.9) (p = 0.575). OS rate and PFS rate are listed. None of efficacy endpoints reached statistical difference. All patients suffered from AEs. No AEs-related death occurred. Conclusions: Efficacy and safety of later-line T+A in uHCC patients was similar with those who used regorafenib plus PD-1 inhibitors, which needed to be further confirmed.

Outcomes.

OutcomesCohort: T+ACohort: Reg+PD-1
PFS (median, 95%CI)5.1 (1.1-9.1)3.5 (2.1-4.9)
3-month PFS rate70.7%60.3%
6-month PFS rate48.5%26.5%
12-month PFS rate12.1%8.8%
OS (median, 95%CI)8.2 (5.8-10.6)15.6 (7.6-23.6)
3-month OS rate90.9%95.2%
6-month OS rate81.8%76.2%
12-month OS rate40.9%60.8%

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Abstract Details

Meeting

2023 ASCO Annual Meeting

Session Type

Publication Only

Session Title

Publication Only: Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Track

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Sub Track

Hepatobiliary Cancer - Advanced/Metastatic Disease

Citation

J Clin Oncol 41, 2023 (suppl 16; abstr e16173)

DOI

10.1200/JCO.2023.41.16_suppl.e16173

Abstract #

e16173

Abstract Disclosures