作者
Akifumi Kuwano,Masayoshi Yada,Kosuke Tanaka,Taikan Hamomoto,Kazuki Kurosaka,Hideo Suzuki,Kenta Motomura
摘要
Background/Aim:
The optimal systemic therapy for intermediate-stage (BCLC-B) hepatocellular carcinoma (HCC) remains undefined. While transarterial chemoembolization (TACE) has long been the standard of care, increasing use of molecular-targeted agents and immune checkpoint inhibitors (ICIs), including atezolizumab plus bevacizumab (Atez/Bev) and lenvatinib (LEN), has shifted therapeutic paradigms. This study compared real-world effectiveness, safety, and cost-effectiveness of Atez/Bev versus LEN for BCLC-B HCC in Japan. Patients and Methods:
This single-center, retrospective cohort study analyzed 55 consecutive patients with BCLC-B HCC: 33 received Atez/Bev and 22 received lenvatinib. Clinical outcomes, treatment-related adverse events, total healthcare expenditures (drugs costs, hospitalization, procedures, imaging, laboratory tests, supportive care) were assessed. Life-years gained (LYG) were estimated using mean overall survival, and incremental cost-effectiveness ratios (ICERs) were calculated. Results:
Baseline age and body weight were comparable between groups. The Atez/Bev cohort had larger tumors and more impaired liver function. No significant differences were observed in tumor response, median overall survival (OS), or progression-free survival (PFS). Mean total healthcare expenditures per patient were significantly lower with lenvatinib ($65,227.9) than with Atez/Bev ($101,480.1; p=0.036), primarily as a result of reduced drug acquisition costs (Atez/Bev: $70,000; LEN: $33,241.4; p=0.007). Life-years lost with Atez/Bev versus LEN totaled 0.46 years (mean OS: Atez/Bev: 17.82 months; LEN: 23.27 months). LEN dominated Atez/Bev (ICER=−$161,896.5 per LYG). Conclusion:
Although Atez/Bev and LEN confer similar survival in BCLC-B HCC, lenvatinib offers superior cost-effectiveness in the Japanese healthcare setting. These findings underscore the importance of integrating economic considerations into treatment selection for intermediate-stage HCC.