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. 2024 May 24:14:1374262.
doi: 10.3389/fonc.2024.1374262. eCollection 2024.

Can adjuvant immune checkpoint inhibitors improve the long-term outcomes of hepatocellular carcinoma with high-risk recurrent factors after liver resection? A meta-analysis and systematic review

Affiliations

Can adjuvant immune checkpoint inhibitors improve the long-term outcomes of hepatocellular carcinoma with high-risk recurrent factors after liver resection? A meta-analysis and systematic review

Lingbo Hu et al. Front Oncol. .

Abstract

Background: Administering adjuvant therapy following liver resection is crucial for patients with hepatocellular carcinoma (HCC) exhibiting high-risk recurrence factors. Immune checkpoint inhibitors (ICIs) are effective against unresectable HCC; however, their effectiveness and safety for this specific patient group remain uncertain.

Methods: We conducted an extensive literature search across four scholarly databases to identify relevant studies. Our primary endpoints were overall survival (OS), recurrence-free survival (RFS), and adverse events (AEs). OS and RFS were quantified using hazard ratios (HRs), whereas the 1-, 2-, and 3-year OS and RFS rates were expressed as risk ratios (RRs). Additionally, the incidence of AEs was calculated.

Results: Our meta-analysis included 11 studies (N = 3,219 patients), comprising two randomized controlled trials (RCTs) and nine retrospective studies. Among these, eight studies reported HRs for OS, showing a statistically significant improvement in OS among patients receiving adjuvant ICIs (HR, 0.60; 95% confidence interval [CI], 0.45-0.80; p < 0.0001). All included studies reported HRs for RFS, indicating a favorable impact of adjuvant ICIs (HR, 0.62; 95% CI, 0.52-0.73; p < 0.0001). Moreover, aggregated data demonstrated improved 1- and 2-year OS and RFS rates with adjuvant ICIs. The incidence rate of AEs of any grade was 0.70 (95% CI, 0.49-0.91), with grade 3 or above AEs occurring at a rate of 0.12 (95% CI, 0.05-0.20).

Conclusion: Adjuvant ICI therapy can enhance both OS and RFS rates in patients with HCC exhibiting high-risk recurrence factors, with manageable AEs.

Systematic review registration: https://www.crd.york.ac.uk/prospero/#recordDetails PROSPERO, identifier CRD42023488250.

Keywords: adjuvant therapy; hepatocellular carcinoma; immune checkpoint inhibitors; liver resection; prognosis.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Flow chart of literature search.
Figure 2
Figure 2
Forest plot of overall and recurrence-free survival rates. (A) Overall survival; (B) Recurrence-free survival.
Figure 3
Figure 3
Forest plot for 1-, 2-, and 3-year overall and recurrence-free survival rates.
Figure 4
Figure 4
Forest plot of any grade and grade 3 or 4 adverse events. (A) Any grade adverse events; (B) Grade 3 or 4 adverse events.
Figure 5
Figure 5
Subgroup analysis for overall survival. Abbreviations: PSM, propensity score matching; MVI, microvascular invasion; ES, Edmondson-Steiner; AFP, alpha-fetoprotein; BCLC, Barcelona Clinic Liver Cancer; ICI, immune checkpoint inhibitor; TACE, transarterial chemoembolization; TKI, tyrosine kinase inhibitor.
Figure 6
Figure 6
Subgroup analysis for recurrence-free survival. Abbreviations: PSM, propensity score matching; MVI, microvascular invasion; ES, Edmondson-Steiner; AFP, alpha-fetoprotein; BCLC, Barcelona Clinic Liver Cancer; ICI, immune checkpoint inhibitor; TACE, transarterial chemoembolization; TKI, tyrosine kinase inhibitor.

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