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Endovasscular iodine-125 seeds strand brachytherapy combined with stent placement and TACE for treatment of HCC complicated by tumor thrombus in main portal vein

Endovasscular iodine-125 seeds strand brachytherapy combined with stent placement and TACE for treatment of HCC complicated by tumor thrombus in main portal vein

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001500
Enrollment
Unknown
Registered
2011-08-30
Start date
2009-05-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular carcinoma

Interventions

1:Iodine-125 seeds strand and stent were placed in the obstucted MPV combined with TACE
2:Stent was placed in the obstructed MPV combined with TACE

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. diagnosis of HCC confirmed by histology, cytology, or persistently elevated serum alpha-fetoprotein (AFP) (> 400ng/ml) with typical imaging findings; 2. the unsuitability of HCC for resection, liver transplantation or percutaneous ablation according to Barcelona Clinical Liver Cancer (BCLC) staging classification; 3. MPV tumor thrombus was diagnosed by the imaging criteria: filling defect with enhancement was founded in MPV on the arterial phase of enhanced computed tomography (CT) or magnetic resonance imaging (MRI) scan before therapy; 4. at least, the second-order branch of the intrahepatic portal vein being patent in one lobe; 5. no prior therapy for MPV tumor thrombus; 6. Child-Pugh classification grade A or B; 7. Eastern Cooperative Oncology Group (ECOG) performance status < 2.

Exclusion criteria

Exclusion criteria: 1. refused to endovascular brachytherapy or cannot follow the study protocol; 2. intrahepatic portal vein completely occluded by HCC; 3. superior mesenteric vein or splenic vein or both involved by tumor thrombus; 4. contraindications for TACE, including HCC burden> 50% of total liver volume, high flow intrahepatic arteriovenous shunt, total bilirubin >51umol/L, albumin5 times upper limit of normal range, creatinine >115umol/L, leukocyte count 6s above control.

Design outcomes

Primary

MeasureTime frame
survival time;

Secondary

MeasureTime frame
stent patency;

Countries

China

Contacts

Public ContactZhiping Yan
yan.zhiping@zs-hospital.sh..cn+86 021 6404990-2533

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026