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3D-MRE-based DLR model to predict status of intratumoral tertiary lymphoid structures in HCC and evaluate biological mechanisms

3D-MRE-based DLR model to predict status of intratumoral tertiary lymphoid structures in HCC and evaluate biological mechanisms

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118431
Enrollment
Unknown
Registered
2026-02-05
Start date
2025-01-01
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

Hepatocellular Carcinoma

Interventions

Sponsors

Xiangya Hospital Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Inclusion criterias for surgery cohort: 1) patients who underwent mp-MRI and 3D-MRE examinations preoperatively; 2) patients with HCC confirmed by postoperative pathology; 3) an interval of no more than two months between the surgical resection and the MRE examination. 2.Inclusion criterias for immunotherapy cohort: 1) unresectable, locally advanced or metastatic HCC diagnosed histologically or radiologically based on American Association for the Study of Liver Diseases (AASLD) criteria; 2) liver function: Child-Pugh class A; 3) at least one measurable tumor lesion as defined by the modified Response Evaluation Criteria in Solid Tumors (mRECIST); 4) planned treatment with an immune checkpoint inhibitor (ICI)-based regimen as the initial first-line therapy; 5) Eastern Cooperative Oncology Group (ECOG) performance status of 0-1; 6) underwent mp-MRI and 3D-MRE examinations before treatment; 7) Age >= 18 years.

Exclusion criteria

Exclusion criteria: 1.Exclusion criterias for surgery cohort: 1)patients who received any other anti-tumor therapy prior to surgery (e.g., previous surgery, interventional therapy, or systemic therapy); 2) Incomplete 3D-MRE or mp-MRI data, or poor image quality; 3) Incomplete pathological data. 2.Exclusion criterias for immunotherapy cohort: 1) concurrent or history of other active malignancies; 2) prior local therapy for HCC lesions or any systemic therapy other than immunotherapy; 3) lack of regular follow-up imaging examinations; 4) follow-up duration of less than six months; 5) incomplete baseline clinical laboratory data; 6) an interval exceeding half a month between the MRI examination (or clinical laboratory tests) and the initiation of therapy.

Design outcomes

Primary

MeasureTime frame
Positive predictive value;Negative predictive value;

Secondary

MeasureTime frame
sensitivity;specificity;

Countries

China

Contacts

Public ContactLi Mengsi

Xiangya Hospital Central South University

limengsi@csu.edu.cn+86 151 1113 4264

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026