Clinical trial · Observational
Blood Sample Collection to Evaluate Biomarkers for Hepatocellular Carcinoma
2017-01: Blood Sample Collection to Evaluate Biomarkers for Hepatocellular Carcinoma
NCT03628651CI-TRIAL-00046462completedClinicalTrials.gov clinicaltrialsProvenance
- 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 primary objective of this study is to obtain de-identified, clinically-characterized whole blood specimens for use in developing and evaluating the performance of new biomarker assays for detection of hepatocellular carcinoma (HCC).
Conditions
Conditions (2)
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 |
| Hepatocellular Carcinoma Surveillance | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Blood Sample Collection | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- HCC Surveillance
- description
- Approximately 1400 HCC surveillance subjects (controls) will be enrolled.
- interventionNames
- Other: Blood Sample Collection
- label
- HCC
- description
- Approximately 700 subjects with untreated clinically diagnosed HCC will be enrolled.
- interventionNames
- Other: Blood Sample Collection
Primary outcomes (1)
- measure
- Biomarker Identification
- timeFrame
- 1 year
- description
- Biomarkers under evaluation include differential methylation of nucleic acids and altered expression of proteins in blood from subjects with HCC compared to those without (but are at risk of developing the disease so are under surveillance)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * All Subjects: 1. Subject is 18 years of age or older 2. Subject understands the study procedures and is able to provide informed consent to participate in the study and authorization for release of data, including personal health data, to the study investigator and sponsor HCC Subjects: 1\. Subject has a recent (within 6 months of enrollment) untreated clinically diagnosed hepatocellular carcinoma as defined by ≥1 cm lesion exhibiting arterial phase hyperenhancement in combination with washout appearance and/or capsule by 4 phase CT scan or multiphase contrast enhanced MRI or biopsy is positive for HCC. Control Subjects: 1. Non-cancer subject undergoing routine imaging surveillance for HCC 2. Definitive lack of HCC within 3 months prior to enrollment as defined by negative imaging, for HCC. 1. Control Group 1 - negative by ultrasound 2. Control Group 2 - negative by CT or MRI Exclusion Criteria: 1. Known cancer diagnosis within the past 5 years (with the exceptions of basal cell or squamous cell skin cancers). 2. Chemotherapy and/or radiation therapy within 5 years prior to enrollment/sample collection. 3. Prior or current treatment with sorafenib, regorafenib, or other treatment indicated for HCC. 4. Any HCC treatment prior to enrollment/blood sample collection (e.g., surgery, ablation, embolization, pharmacotherapy, radiotherapy, liver transplant or other treatment indicated for HCC). 5. IV contrast (e.g. CT and MRI) within 1 day \[or 24 hours\] of blood collection. 6. Less than 3 days between fine needle aspiration (FNA) of target pathology and blood collection. 7. Less than 7 days between biopsy (other than FNA) of target pathology and blood collection. 8. Individual has a condition the Investigator believes would interfere with his or her ability to provide informed consent, comply with the study protocol, which might confound the interpretation of the study results or put the person at undue risk.
References
Publications (2)
- DERIVEDChalasani NP, Porter K, Bhattacharya A, Book AJ, Neis BM, Xiong KM, Ramasubramanian TS, Edwards DK 5th, Chen I, Johnson S, Roberts LR, Kisiel JB, Reddy KR, Singal AG, Olson MC, Bruinsma JJ. Validation of a Novel Multitarget Blood Test Shows High Sensitivity to Detect Early Stage Hepatocellular Carcinoma. Clin Gastroenterol Hepatol. 2022 Jan;20(1):173-182.e7. doi: 10.1016/j.cgh.2021.08.010. Epub 2021 Aug 13. PMID 34391922
- DERIVEDChalasani NP, Ramasubramanian TS, Bhattacharya A, Olson MC, Edwards V DK, Roberts LR, Kisiel JB, Reddy KR, Lidgard GP, Johnson SC, Bruinsma JJ. A Novel Blood-Based Panel of Methylated DNA and Protein Markers for Detection of Early-Stage Hepatocellular Carcinoma. Clin Gastroenterol Hepatol. 2021 Dec;19(12):2597-2605.e4. doi: 10.1016/j.cgh.2020.08.065. Epub 2020 Sep 2. PMID 32889146