Health Condition 1: C220- Liver cell carcinoma
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
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 3 g/dL, international normalized ratio [INR] < 1.5) no (or mild) ascites, not suitable for TACE, and age above 18 years.
Exclusion criteria
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).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Response to treatment with recanalization of portal veinTimepoint: 10 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| survival function, toxicity parameters, factors influencing response to treatment, and feasibility of TACE/TARE in responders.Timepoint: 6 months, 1 year, 2 year | — |
Countries
India
Contacts
Amrita Institute of Medical Sciences