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Advantage of Scheduled Upfront Lenvatinib Administration Followed by Transarterial Chemoembolization Therapy Over Lenvatinib Monotherapy in Patients With Unresectable Intermediate-Stage Hepatocellular Carcinoma: A Multicenter Cohort Study.

코호트 1/5 보강
Cancer medicine 📖 저널 OA 95.5% 2022: 15/15 OA 2023: 14/14 OA 2024: 36/36 OA 2025: 164/164 OA 2026: 211/232 OA 2022~2026 2026 Vol.15(1) p. e71503
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 3/4)

유사 논문
P · Population 대상 환자/모집단
41 patients with unresectable Barcelona Clinic Liver Cancer intermediate-stage HCC who were considered unsuitable for TACE owing to factors such as exceeding the up-to-7 criteria, having infiltrative HCC, or multiple asynchronous recurrent HCC.
I · Intervention 중재 / 시술
lenvatinib monotherapy
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Superiority in both PFS and OS was also observed in the propensity score-matched (PSM) cohort for the LEN-TACE group. [CONCLUSION] Scheduled upfront lenvatinib combined with TACE is superior to lenvatinib monotherapy for intermediate-stage HCC, particularly in patients unsuitable for TACE.

Taniki N, Ojiro K, Kasuga R, Nakadai Y, Tabuchi T, Chu PS, Usui S, Hoshi H, Kaneko F, Yamaguchi A, Koizumi J, Ebinuma H, Tamura M, Tsukada J, Inoue M, Nakatsuka S, Hasegawa Y, Abe Y, Kitago M, Jinzaki M, Kitagawa Y, Kanai T, Nakamoto N

📝 환자 설명용 한 줄

[BACKGROUND AND AIM] Combining systemic chemotherapy with transarterial chemoembolization (TACE) has demonstrated improved outcomes, with promising results for the efficacy of lenvatinib pretreatment

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • p-value p = 0.0496
  • 95% CI 1.01-8.95

이 논문을 인용하기

↓ .bib ↓ .ris
APA Taniki N, Ojiro K, et al. (2026). Advantage of Scheduled Upfront Lenvatinib Administration Followed by Transarterial Chemoembolization Therapy Over Lenvatinib Monotherapy in Patients With Unresectable Intermediate-Stage Hepatocellular Carcinoma: A Multicenter Cohort Study.. Cancer medicine, 15(1), e71503. https://doi.org/10.1002/cam4.71503
MLA Taniki N, et al.. "Advantage of Scheduled Upfront Lenvatinib Administration Followed by Transarterial Chemoembolization Therapy Over Lenvatinib Monotherapy in Patients With Unresectable Intermediate-Stage Hepatocellular Carcinoma: A Multicenter Cohort Study.." Cancer medicine, vol. 15, no. 1, 2026, pp. e71503.
PMID 41546425 ↗
DOI 10.1002/cam4.71503

Abstract

[BACKGROUND AND AIM] Combining systemic chemotherapy with transarterial chemoembolization (TACE) has demonstrated improved outcomes, with promising results for the efficacy of lenvatinib pretreatment combined with TACE in single-arm studies involving patients with hepatocellular carcinoma (HCC). This study aimed to evaluate the efficacy of a scheduled upfront lenvatinib combined with a TACE regimen in patients with HCC, representing both the first study to comparatively analyze this approach and to focus specifically on patients unsuitable for TACE.

[METHODS] We conducted a multicenter retrospective study between 2018 and 2024, enrolling 41 patients with unresectable Barcelona Clinic Liver Cancer intermediate-stage HCC who were considered unsuitable for TACE owing to factors such as exceeding the up-to-7 criteria, having infiltrative HCC, or multiple asynchronous recurrent HCC. Of these patients, 25 received upfront lenvatinib administration prior to TACE (LEN-TACE group), followed by continuous lenvatinib and on-demand TACE, and 16 received lenvatinib monotherapy.

[RESULTS] Radiological evaluation revealed significantly higher complete response (CR) and objective response rates (ORR) in the LEN-TACE group than in the lenvatinib group. The median overall survival (OS) was not reached in the LEN-TACE group, whereas it was 16.2 months in the lenvatinib monotherapy group, indicating a significantly superior OS in the LEN-TACE group (hazard ratio [HR]: 2.99; 95% CI: 1.01-8.95; p = 0.0496). Superiority in both PFS and OS was also observed in the propensity score-matched (PSM) cohort for the LEN-TACE group.

[CONCLUSION] Scheduled upfront lenvatinib combined with TACE is superior to lenvatinib monotherapy for intermediate-stage HCC, particularly in patients unsuitable for TACE.

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