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논문 기본 정보

자료유형
학술저널
저자정보
박재연 (Seoul National University College of Medicine, Seoul, Korea) 이윤빈 (서울대학교병원) 고윤미 (Seoul National University College of Medicine, Seoul, Korea) 박영수 (Seoul National University College of Medicine, Seoul, Korea) 신현재 (Seoul National University College of Medicine, Seoul, Korea) 허문행 (서울대학교병원) 박민경 (서울대학교병원) 이대원 (서울대학교) 조은주 (서울대학교병원) 이경훈 (서울대학교병원) 이정훈 (서울대학교병원) 유수종 (서울대학교병원) 김태용 (서울대학교) 김태유 (서울대학교병원 내과) 윤정환 (서울대학교)
저널정보
대한간암학회 Journal of Liver Cancer Journal of Liver Cancer 제24권 제1호
발행연도
2024.3
수록면
81 - 91 (11page)
DOI
10.17998/jlc.2023.12.25

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Background/Aim: Atezolizumab plus bevacizumab and lenvatinib are currently available as first-line therapy for the treatment of unresectable hepatocellular carcinoma (HCC). However, comparative efficacy studies are still limited. This study aimed to investigate the effectiveness of these treatments in HCC patients with portal vein tumor thrombosis (PVTT). Methods: We retrospectively included patients who received either atezolizumab plus bevacizumab or lenvatinib as first-line systemic therapy for HCC with PVTT. Primary endpoint was overall survival (OS), and secondary endpoints included progressionfree survival (PFS) and disease control rate (DCR) determined by response evaluation criteria in solid tumors, version 1.1. Results: A total of 52 patients were included: 30 received atezolizumab plus bevacizumab and 22 received lenvatinib. The median follow-up duration was 6.4 months (interquartile range, 3.9-9.8). The median OS was 10.8 months (95% confidence interval [CI], 5.7 to not estimated) with atezolizumab plus bevacizumab and 5.8 months (95% CI, 4.8 to not estimated) with lenvatinib (P=0.26 by log-rank test). There was no statistically significant difference in OS (adjusted hazard ratio [aHR], 0.71; 95% CI, 0.34-1.49; P=0.37). The median PFS was similar (P=0.63 by log-rank test), with 4.1 months (95% CI, 3.3-7.7) for atezolizumab plus bevacizumab and 4.3 months (95% CI, 2.6-5.8) for lenvatinib (aHR, 0.93; 95% CI, 0.51-1.69; P=0.80). HRs were similar after inverse probability treatment weighting. The DCRs were 23.3% and 18.2% in patients receiving atezolizumab plus bevacizumab and lenvatinib, respectively (P=0.74). Conclusion: The effectiveness of atezolizumab plus bevacizumab and lenvatinib was comparable for the treatment of HCC with PVTT.

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