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Background: The efficacy of transarterial chemoembolization (TACE) in treating unresectable hepatocellular carcinoma (uHCC) complicated by arterioportal shunts (APS) was unsatisfactory. Developed systemic therapies can synergize with TACE, potentially reducing APS recanalization and enhancing patient benefits. The objective of this study was to evaluate and compare the therapeutic efficacy and safety of a combination therapy regimen that includes TACE, lenvatinib, and sintilimab (TACE-L-S) versus TACE monotherapy in uHCC patients with APS.
Methods: After reviewing hospital records, this retrospective study enrolled 96 patients: 51 in the TACE-L-S group and 45 in the TACE group. We utilized the Chi-squared test to analyze tumor response, changes in APS grades, APS recanalization rates, and adverse events (AEs) between the two groups. Kaplan-Meier analysis was employed to compare median progression-free survival (mPFS). Cox regression analyses were conducted to identify factors influencing mPFS, whereas logistic regression analyses were performed to assess factors influencing APS recanalization rates.
Results: The objective response rate (ORR) was 68.6% in the TACE-L-S group and 37.8% in the TACE group (P=0.002). The TACE-L-S group had better mPFS compared to the TACE group (168 111 days, P<0.001), influenced by the treatment option, hepatic vein invasion, and portal vein tumor thrombosis (PVTT) type. Following the first TACE procedure, APS grades were similar between the groups; however, at 3 months after the first TACE, the TACE-L-S group demonstrated better APS grades. APS recanalization rates also differed significantly between the groups (24.4% 53.8%, P=0.006), influenced by the treatment option, preoperative APS grade, and PVTT type. AEs associated with TACE-L-S were tolerable.
Conclusions: For uHCC patients with APS, TACE-L-S may be a kind of effective and safe therapy.
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http://dx.doi.org/10.21037/tcr-2025-167 | DOI Listing |
Front Immunol
July 2025
Neurology Department, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Background: The pathogenic potential of non-criteria antiphospholipid antibodies (aPLs), such as anti-β2-glycoprotein I (aβ2GPI) IgA, remains undefined. Additionally, the role of antiplatelet therapy in thrombotic antiphospholipid syndrome (APS) is controversial. Diagnosing APS is challenging when consensus aPLs are negative.
View Article and Find Full Text PDFTransl Cancer Res
June 2025
Interventional Therapy Department, Ningbo No. 2 Hospital, Ningbo, China.
Background: The efficacy of transarterial chemoembolization (TACE) in treating unresectable hepatocellular carcinoma (uHCC) complicated by arterioportal shunts (APS) was unsatisfactory. Developed systemic therapies can synergize with TACE, potentially reducing APS recanalization and enhancing patient benefits. The objective of this study was to evaluate and compare the therapeutic efficacy and safety of a combination therapy regimen that includes TACE, lenvatinib, and sintilimab (TACE-L-S) versus TACE monotherapy in uHCC patients with APS.
View Article and Find Full Text PDFAnn Med Surg (Lond)
June 2025
Department of Internal Medicine, Al-Ahli Hospital, West Bank, Palestine.
Introduction And Importance: Neurologic disorders are among the most significant clinical symptoms of systemic lupus erythematosus (SLE) and antiphospholipid syndrome (APS), primarily affecting the central nervous system. Both SLE and APS increase the risk of cerebrovascular events, and stroke is one of the most serious and late consequences that often occur years after diagnosis. Stroke as an initial symptom is uncommon in its early stages and frequently misinterpreted as ischemic cerebrovascular illness, posing diagnostic challenges.
View Article and Find Full Text PDFAliment Pharmacol Ther
March 2025
Division of Gastroenterology and Hepatology, Department of Medicine, University of Pennsylvania, Philadelphia, USA.
Background And Aims: We assessed clinical, procoagulant and genetic risk factors and clinical outcomes in dabigatran-treated patients with non-tumoural acute and acute-on-chronic portal vein thrombosis (PVT).
Methods: Patients with a new diagnosis of non-tumoural acute and acute-on-chronic PVT between January 2021 and January 2024 (aged ≥ 18 years) in those without/with cirrhosis (Child-Pugh (CP)-A/B/C ≤ 10) were started on dabigatran and followed and compared with those on vitamin K antagonist (VKA) and untreated individuals.
Results: Dabigatran was prescribed in 119 patients with PVT type 1 (61, 51.
Clin Rheumatol
December 2024
Department of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.