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Cyberknife Radiosurgery in Hepatocellular carcinoma with Portal vein tumor thrombosis

Phase 2
Conditions
Health Condition 1: C220- Liver cell carcinoma
Registration Number
CTRI/2022/02/040384
Lead Sponsor
Amrita Institute of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients with radiologically confirmed HCC with

portal vein invasion, willing to participate in the study, having good performance statusâ??Eastern Cooperative Oncology Group (ECOG)â??0 to 2 preserved liver function (bilirubin <4 mg/dL, preferably albumin >3 g/dL, international normalized ratio [INR] < 1.5) no (or mild) ascites, not suitable for TACE, and age above 18 years.

Exclusion Criteria

Patients not consenting for the study, poor performance status (ECOG 3â??4), extrahepatic visceral metastases, long PVT involvement ( >7 cm in axial length), Child C with decompensated liver function, large HCC ( >10 cm cumulative length of the mass), and previously treated with radiation therapy for liver lesion and patients who underwent transarterial radioembolization (TARE).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Response to treatment with recanalization of portal veinTimepoint: 10 weeks
Secondary Outcome Measures
NameTimeMethod
survival function, toxicity parameters, factors influencing <br/ ><br>response to treatment, and feasibility of TACE/TARE in <br/ ><br>responders.Timepoint: 6 months, 1 year, 2 year
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