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Research on Predicting Treatment Response and Prognosis of Brain Tumors Based on Radiomics and Pathomics

Research on Predicting Treatment Response and Prognosis of Brain Tumors Based on Radiomics and Pathomics

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121227
Enrollment
Unknown
Registered
2026-03-27
Start date
2026-03-27
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Brain tumors that meet the histomorphological characteristics and related pathological indicators of the World Health Organization Classification of Tumors of the Central Nervous System (WHO 2021 5th edition).

Interventions

Sponsors

Yuebei People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years, regardless of gender; 2.Pathologically confirmed diagnosis of brain tumor, with complete histopathological sections or digital pathological image data available; 3.Received a clearly defined specific treatment modality (e.g., surgery, radiotherapy, chemoradiotherapy, or other treatment protocols specified in the study), with complete records of the treatment regimen; 4.Pretreatment MRI data meeting the study requirements (including routine sequences and specific sequences required for the study), with image quality satisfying the standards for radiomics analysis; 5.Complete clinical follow-up data available to clearly evaluate treatment response and related outcomes (including poor prognosis, functional impairment, postoperative progression, radiation necrosis, etc.);

Exclusion criteria

Exclusion criteria: 1.Prior intervention treatments (e.g., surgery or radiotherapy at other institutions) received before the current treatment, with effects that cannot be clearly delineated; 2.Comorbid severe systemic diseases or other malignant tumors that may significantly affect prognosis assessment; 3.Excessive time interval between imaging and pathological data acquisition;

Design outcomes

Primary

MeasureTime frame
Treatment response;

Secondary

MeasureTime frame
Postoperative complications;

Countries

China

Contacts

Public ContactLiu Xiang

Yuebei People’s Hospital

liuxiangxl72@163.com+86 751 6913416

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 4, 2026