# Usefulness of atezolizumab plus bevacizumab as second-line therapy for patients with unresectable hepatocellular carcinoma

**Authors:** Shinpei Yamaba, Yukinori Imai, Kayoko Sugawara, Yoshihito Uchida, Akira Fuchigami, Hiroshi Uchiya, Nobuaki Nakayama, Satoshi Mochida, Jincheng Wang, Jincheng Wang

PMC · DOI: 10.1371/journal.pone.0298770 · PLOS ONE · 2024-04-30

## TL;DR

A combination of atezolizumab and bevacizumab shows promise as a second-line treatment for advanced liver cancer, with similar survival rates in patients who had prior therapies.

## Contribution

The study evaluates the effectiveness of atezolizumab plus bevacizumab in MTA-experienced hepatocellular carcinoma patients.

## Key findings

- The combination therapy achieved an overall response rate of 32.8% and a disease control rate of 82.1%.
- Patients who had not previously received molecular-targeted agents had a higher response rate (40.5%) compared to those who had (7.7%).
- Survival rates at 24 and 48 weeks were 86% and 72%, with no significant difference between MTA-naïve and MTA-experienced patients.

## Abstract

To clarify the efficacy of atezolizumab (ATZ) plus bevacizumab (BEV) as the second-line therapy for patients with unresectable hepatocellular carcinoma (HCC).

The subjects were 82 patients with HCC receiving ATZ/BEV, including 33 patients with previous therapies with molecular-targeted agents (MTA). Therapeutic efficacy was evaluated using contrast-enhanced CT according to the mRECIST.

The Child-Pugh scores were 5, 6,7 and 8 in 40, 35, 5 and 2 patients, respectively, and the extents of HCC progression were BCLC stage A, B and C in 3, 31 and 48 patients, respectively. Early therapeutic efficacy was evaluated in 67 patients, and percentages of patients achieving CR/PR/SD/PD until 12 weeks were 3.0%/29.9%/49.3%/17.9%, respectively, indicating ORR of 32.8% and DCR of 82.1%, The ORR was higher in MTA-naïve patients (40.5%) than in those after discontinuation of lenvatinib due to PD (7.7%, P = 0.0410), while the DCR was equivalent between both patients (83.3% vs 80.0%, P = 0.1184), and the multivariate analysis revealed previous MTA therapies with lenvatinib alone as a factor to deteriorate the ORR (HR of 4.846 (P = 0.0619)). The OS rates at 24 and 48 weeks were 86% and 72%, respectively, and the rates did not differ between MTA-naïve and MTA-experienced patients. Multivariate analyses revealed that achievement of CR, PR or SD and peripheral neutrophil/lymphocyte ratio were associated with a favorable outcome (HR of 0.124, P<0.0001 and 0.351, P = 0.0303).

ATZ/BEV merits consideration even for MTA-experienced patients, since the OS was equivalent to those in MTA-naïve patients despite of an unfavorable early therapeutic efficacy.

## Linked entities

- **Chemicals:** lenvatinib (PubChem CID 9823820)
- **Diseases:** hepatocellular carcinoma (MONDO:0007256), liver cancer (MONDO:0002691)

## Full-text entities

- **Diseases:** PD (MESH:D010300), HCC (MESH:D006528)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC11060596/full.md

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Source: https://tomesphere.com/paper/PMC11060596