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Analysis of the evolutionary characteristics of the common tumor immune microenvironment — Screening and validation study of multi-omics-based diagnostic markers for distinguishing benign and malignant tumors of neuroendocrine organs

Analysis of the evolutionary characteristics of the common tumor immune microenvironment — Screening and validation study of multi-omics-based diagnostic markers for distinguishing benign and malignant tumors of neuroendocrine organs

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123670
Enrollment
Unknown
Registered
2026-04-28
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Parathyroid Adenoma

Interventions

Control group (parathyroid adenoma / adrenocortical adenoma):None
Experimental group (parathyroid carcinoma / adrenocortical carcinoma):None

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. All cases were surgically resected parathyroid or adrenocortical tumor tissues, with definitive postoperative pathological diagnoses serving as the grouping criteria. 2.(2) Complete clinicopathological information was available for all cases. 3.(3) Samples were formalin-fixed paraffin-embedded (FFPE) tissues, with quality sufficient for proteomics and other analyses. 4.(4) All subjects were enrolled consecutively. 5.(5) All subjects agreed to participate in the study and signed informed consent forms.

Exclusion criteria

Exclusion criteria: 1. Cases with uncertain pathological diagnosis or inability to distinguish between benign and malignant tumors, and cases related to familial endocrine tumor syndromes; 2. Parathyroid hyperplasia and adrenal cortical hyperplasia; 3. Severe tissue autolysis or RNA/DNA degradation; 4. Patients with previous or concurrent malignant tumors in other organs; 5. Samples from patients who have previously received preoperative radiotherapy, chemotherapy, targeted therapy, or embolization treatment that may alter tumor biological characteristics; 6. Individuals who refuse to participate in this trial or refuse to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Expression levels of candidate biomarkers in tissue samples;

Countries

China

Contacts

Public ContactXiu Nie

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

niexiuyishi@126.com+86 15337177785

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026