Articles Vol. 67 No. 10 25/10/2026

OUTCOMES OF SUBSEQUENT TREATMENT AFTER ATEZOLIZUMAB–BEVACIZUMAB FOR HEPATOCELLULAR CARCINOMA

Vu Hong Thang, Nguyen Thi Thu Huong, Chu Quoc Hoan, Do Quang Huy, Nguyen Xuan Dai, Pham Tuan Anh
DOI: 10.52163/yhc.v67i10.6872
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Abstract

Objective: To evaluate outcomes of subsequent active treatment after atezolizumab–bevacizumab (AB) in patients with hepatocellular carcinoma (HCC).

Methods: This descriptive study combined retrospective and prospective data from K Hospital between 2019 and 2026. Of 238 patients treated with AB, 84 (35.3%) received subsequent active treatment and were included. Tumor response was assessed using mRECIST; PFS2 and OS2 were measured from initiation of subsequent treatment. There was no supportive-care-only control group.

Results: ORR and DCR were 10.7% and 69.0% in the overall cohort and 12.3% and 79.5% among radiologically evaluable patients. Median PFS2 and OS2 were 5.2 and 12.1 months. Progression or discontinuation of AB within ≤3 months was independently associated with poorer OS2 (HR 1.97; 95% CI, 1.04–3.73; p = 0.037). Sorafenib and lenvatinib were used in 54.8% and 35.7% of patients, respectively. No statistically significant difference in PFS2 or OS2 was observed between sorafenib and lenvatinib.

Conclusion: Among selected patients who remained eligible for active treatment after AB, TKIs were the most common subsequent therapies, with the observed survival outcomes reported above. AB treatment duration ≤3 months was associated with poorer OS2 and warrants validation in an independent cohort.

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