Extent of Embolization as an Independent Prognostic Factor in Superselective Conventional Transarterial Chemoembolization for Hepatocellular Carcinoma.
[PURPOSE] Superselective conventional transarterial chemoembolization (ss‑cTACE) guided by angiography-multidetector CT (AMDCT) improves feeder detection but can broaden the treated territory and comp
- 표본수 (n) 136
- p-value p =.01
- p-value p =.003
- 95% CI 1.1-2.5
APA
Okumura K, Ogi T, et al. (2026). Extent of Embolization as an Independent Prognostic Factor in Superselective Conventional Transarterial Chemoembolization for Hepatocellular Carcinoma.. Journal of hepatocellular carcinoma, 13, 573705. https://doi.org/10.2147/JHC.S573705
MLA
Okumura K, et al.. "Extent of Embolization as an Independent Prognostic Factor in Superselective Conventional Transarterial Chemoembolization for Hepatocellular Carcinoma.." Journal of hepatocellular carcinoma, vol. 13, 2026, pp. 573705.
PMID
41782744
Abstract
[PURPOSE] Superselective conventional transarterial chemoembolization (ss‑cTACE) guided by angiography-multidetector CT (AMDCT) improves feeder detection but can broaden the treated territory and compromise hepatic reserve. We asked whether restricting the embolized area to <1 Couinaud sector‑equivalent is associated with better prognosis in treatment‑naïve hepatocellular carcinoma (HCC). Our primary estimand was the covariate‑adjusted hazard ratio (HR) comparing extended (≥1 sector‑equivalent) vs limited (<1 sector‑equivalent) embolization.
[PATIENTS AND METHODS] We conducted a single‑center retrospective cohort including 195 consecutive patients with newly diagnosed HCC who underwent initial ss‑cTACE/AMDCT (2010‑10‑01 to 2023‑08‑31; median age 75 years). Post‑procedural imaging classified patients as Group L (<1 sector‑equivalent; n=136) or Group E (≥1; n=59). Endpoints were progression‑free survival (PFS) and overall survival (OS); liver‑related death was modeled with cause‑specific hazards. Multivariable Cox models were prespecified as primary, with propensity‑score overlap weighting as a complementary sensitivity analysis; short‑term hepatic safety was assessed by post‑TACE ALBI within 1 month.
[RESULTS] Compared with Group L, Group E showed shorter PFS (median 7 vs 12 months; aHR 1.7, 95% CI 1.1-2.5; p =.01) and OS (median 21 vs 33 months; aHR 2.1, 95% CI 1.2-3.5; p =.003). Short‑term hepatic safety did not differ: the post‑TACE ALBI score assessed within 1 month was similar between groups (-2.1 ± 0.4 vs -2.0 ± 0.4; p =.16). In Group L, liver‑related survival exceeded OS (113 vs 57 months; p =.01). Adjusted analyses confirmed embolization extent as an independent prognostic factor beyond stage, tumor burden, location, and liver function (PFS aHR 1.7; OS aHR 2.1). Among Group L decedents, HBV/HCV was independently associated with liver‑related death (OR 6.9, 95% CI 1.8-34; p =0.009).
[CONCLUSION] During initial ss‑cTACE/AMDCT, restricting embolization to <1 sector‑equivalent was associated with longer PFS/OS and fewer liver‑related deaths, supporting treatment planning that minimizes ischemic parenchymal injury, particularly in older or vulnerable patients.
[PATIENTS AND METHODS] We conducted a single‑center retrospective cohort including 195 consecutive patients with newly diagnosed HCC who underwent initial ss‑cTACE/AMDCT (2010‑10‑01 to 2023‑08‑31; median age 75 years). Post‑procedural imaging classified patients as Group L (<1 sector‑equivalent; n=136) or Group E (≥1; n=59). Endpoints were progression‑free survival (PFS) and overall survival (OS); liver‑related death was modeled with cause‑specific hazards. Multivariable Cox models were prespecified as primary, with propensity‑score overlap weighting as a complementary sensitivity analysis; short‑term hepatic safety was assessed by post‑TACE ALBI within 1 month.
[RESULTS] Compared with Group L, Group E showed shorter PFS (median 7 vs 12 months; aHR 1.7, 95% CI 1.1-2.5; p =.01) and OS (median 21 vs 33 months; aHR 2.1, 95% CI 1.2-3.5; p =.003). Short‑term hepatic safety did not differ: the post‑TACE ALBI score assessed within 1 month was similar between groups (-2.1 ± 0.4 vs -2.0 ± 0.4; p =.16). In Group L, liver‑related survival exceeded OS (113 vs 57 months; p =.01). Adjusted analyses confirmed embolization extent as an independent prognostic factor beyond stage, tumor burden, location, and liver function (PFS aHR 1.7; OS aHR 2.1). Among Group L decedents, HBV/HCV was independently associated with liver‑related death (OR 6.9, 95% CI 1.8-34; p =0.009).
[CONCLUSION] During initial ss‑cTACE/AMDCT, restricting embolization to <1 sector‑equivalent was associated with longer PFS/OS and fewer liver‑related deaths, supporting treatment planning that minimizes ischemic parenchymal injury, particularly in older or vulnerable patients.
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