Clinical trial · Observational
The Detection of Small Early Liver Cancer With Natural History Follow up
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The SELINA study will recruit 200 patients with cirrhosis and small HCC and 50 patients with HCC but without cirrhosis (most of whom are expected to have FLD). Blood, urine and liver tissue samples (where available) will be collected for laboratory analysis. In a subgroup of patients (N=80, around 64 patients with HCC with liver cirrhosis and around 16 patients with HCC without liver cirrhosis), additional magnetic resonance liver imaging will be performed. The findings of the SELINA study aim to identify biomarkers that can be used to detect liver cancer at the earliest possible time, something we expect will increase the survival rate of HCC.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hepatocellular Carcinoma | Hepatocellular Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Blood & Urine Samples | Other | — | UNRESOLVED |
| Imaging | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- label
- Small HCC with Cirrhosis
- description
- 200 patients diagnosed with small HCC (as defined in Eligibility Criteria) and cirrhosis
- interventionNames
- Other: Blood & Urine Samples
- label
- Small HCC without Cirrhosis
- description
- 50 patients diagnosed with small HCC (as defined in Eligibility Criteria) but without cirrhosis
- interventionNames
- Other: Blood & Urine Samples
- label
- Imaging Subgroup
- description
- In a subgroup of patients (N=80, around 64 patients with HCC with liver cirrhosis and around 16 patients with HCC without liver cirrhosis), additional magnetic resonance liver imaging \& elastography will be performed
- interventionNames
- Other: Imaging
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 100 Years
Show eligibility criteria text
Inclusion Criteria: 1. Participant is willing and able to give informed consent for participation in the study. 2. Male or Female aged 18 years or above. 3. Diagnosed with small HCC (Barcelona Clinic Liver Cancer Staging Criteria (BCLC) stage 0/A; 1-3 nodules \<3cm, preserved liver function, performance status 0) with liver cirrhosis from any aetiology 4. Diagnosed with small HCC (as above) and without cirrhosis 5. Diagnosis of small HCC shown or confirmed within 3 months of study Visit 1 6. Patients with a diagnosis of HCC that was fully ablated or resected more than 6 months ago and now presenting with a new diagnosis of HCC in a different site in the liver may be included in the study 7. Histological confirmation is required to establish the diagnosis of HCC in patients without cirrhosis (imaging alone is not considered sufficient to establish the diagnosis of HCC). Exclusion Criteria: 1. Patients judged by the investigator to be unsuitable for inclusion in the study (e.g. where the investigator feels that the participant will not be able to comply with the study procedures) 2. HCC with liver cirrhosis at BCLC stage B/C 3. Patients who have had a previous liver transplant (note, it is permitted to enrol patients on the liver transplant waiting list if they fulfil all inclusion/exclusion criteria) 4. Participants of the Pearl study 5. Patients who have had a previous diagnosis of HCC followed by therapy, and now have a recurrence at the same site in the liver 6. Patients who have received HCC specific therapy 3 months prior to study visit 1 (including resection, ablation \[microwave/radiofrequency\]), transarterial chemoembolization \[TACE\], select internal radiation therapy \[SIRT\] or stereotactic body radiation therapy \[SBRT\] 3, chemotherapy, immune modulators and other experimental therapies). Exclusion Criteria for Imaging Subgroup 1\. Any contra-indication to Magnetic Resonance Imaging (MRI) (e.g. claustrophobia, metal implants/fragments, implants, pregnancy, other conditions the scanner operator deems unsafe for MR scanning).
References
Publications (0)
Data not yet available