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A multicenter prospective observational study to assess the feasibility of biomarker testing in pediatric liver tumors.

A multicenter prospective observational study to assess the feasibility of biomarker testing in pediatric liver tumors. - JPLT-5

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000056899
Enrollment
20
Registered
2025-02-10
Start date
2025-03-03
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Pediatric liver tumor(hepatoblastoma, HCN-NOS, hepatocellular carcinoma)

Interventions

None listed

Sponsors

pediatric liver tumor committee of Japan Children's Cancer Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Diagnosed or suspected primary childhood liver tumor (hepatoblastoma, HCN-NOS, hepatocellular carcinoma) 2. Age at diagnosis is less than 18 years 3. Written informed consent has been obtained from the patient or a surrogate 4. Informed consent has been obtained for central pathological review and genetic analysis in an observational study of pediatric solid tumors 5. Plasma (serum) samples can be collected before, during and after treatment 6. Clinical, imaging and pathological findings can be collected at diagnosis, during and after treatment

Exclusion criteria

Exclusion criteria: If the physicians at each facility determine that participation of patient in the study is not appropriate

Design outcomes

Primary

MeasureTime frame
Number of days between submission of tumour specimens for molecular genetic analysis (biomarker analysis) and obtain of results of methylation analysis tested by ddPCR method (turnaround time; TAT).

Countries

Japan

Contacts

Public ContactJunya Fujimura

Juntendo university Department of pediatrics

junya-f@juntendo.ac.jp03-3813-3111ext3325

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026