Skip to content

An observational study evaluating role of highly dose conformal radiotherapy in management of portal vein tumour thrombus in a case of HCC

Outcomes of Stereotactic Body Radiotherapy in the Management of Portal Vein tumour Thrombosis in Hepatocellular Carcinoma: An Observational Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/07/091458
Enrollment
15
Registered
2025-07-22
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: C220- Liver cell carcinoma

Interventions

Intervention1: Nil: Nil

Sponsors

Department of Radiotherapy and Clinical Oncology, PGIMER, Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosis of Hepatocellular Carcinoma (HCC) with radiologically or histologically confirmed portal vein tumor thrombosis (PVTT). 2. ECOG Performance Status of 0 2 3. BCLC stage C 4. Child-Pugh Class A or B liver function status 5. Adequate remaining liver volume, defined as at least 700 cc of uninvolved liver tissue.

Exclusion criteria

Exclusion criteria: 1. Presence of metastatic disease outside the liver. 2. Previous radiotherapy to the liver. 3. Child-Pugh Class C liver function status with Child pugh score of 10 to 15.

Design outcomes

Primary

MeasureTime frame
1.To evaluate the radiological response of portal vein tumor thrombus (PVTT) following SBRT using mRECIST criteria, assessing changes in tumor viability based on arterial-phase enhancement and measuring PVTT size pre- and post-SBRT at 2, 4, and 6 months. 2.We will also measure the biochemical level of AFP and PIVKAA II before SBRT and after SBRT at 2 months ,4 months and 6 months. Timepoint: 1.To evaluate the radiological response of portal vein tumor thrombus (PVTT) following SBRT using mRECIST criteria, assessing changes in tumor viability based on arterial-phase enhancement and measuring PVTT size pre- and post-SBRT at 2, 4, and 6 months. 2.We will also measure the biochemical level of AFP and PIVKAA II before SBRT and after SBRT at 2 months ,4 months and 6 months.

Secondary

MeasureTime frame
1. To assess acute toxicity profile of SBRT in patients with PVTT, using RTOG scoring criteria.Timepoint: at third fraction 1month 2month

Countries

India

Contacts

Public ContactDr Rakesh Kapoor

Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh

drkapoor.r@gmail.com9872648344

Outcome results

None listed

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