Skip to content

A Bidirectional Cohort Study of Primary Central Nervous System Lymphoma Patients

A Bidirectional Cohort Study of Primary Central Nervous System Lymphoma Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101089
Enrollment
Unknown
Registered
2025-04-20
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Clinical Presentation of Primary Central Nervous System Lymphoma (PCNSL): The clinical symptoms of PCNSL depend on the tumor's location within the central nervous system. Common manifestations include ?headache, ?seizures, ?focal neurological deficits, ?personality or cognitive alterations, and ?signs of elevated intracranial pressure (e.g., papilledema, nausea/vomiting). Approximately ?10%–20% o

Interventions

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Prospective cohort study part: Age >= 18 years, regardless of gender; diagnosed with primary central nervous system lymphoma (PCNSL) according to EANO guidelines, with lesions limited to the central nervous system (brain, spinal cord, eyes, or leptomeninges), without evidence of systemic lymphoma; clinical plan to perform surgical biopsy or stereotactic biopsy to obtain clear histopathological diagnosis; the subject or their legal representative has fully understood the research content and voluntarily signed the informed consent form; patients who sought medical care at Southern Hospital of Southern Medical University between January 2025 and December 2030. 2.Retrospective cohort study part (requiring informed consent): Age >= 18 years, regardless of gender; diagnosed with primary central nervous system lymphoma (PCNSL) according to EANO guidelines, with lesions limited to the central nervous system (brain, spinal cord, eyes, or leptomeninges), without evidence of systemic lymphoma; clinical surgical biopsy or stereotactic biopsy has been performed to obtain clear histopathological diagnosis; the subject or their legal representative has fully understood the research content and voluntarily signed the informed consent form; patients who sought medical care at Southern Hospital of Southern Medical University between January 2024 and December 2024. 3.Retrospective cohort study part (proposing waiver of informed consent): Age >= 18 years, regardless of gender; diagnosed with primary central nervous system lymphoma (PCNSL) according to EANO guidelines, with lesions limited to the central nervous system (brain, spinal cord, eyes, or leptomeninges), without evidence of systemic lymphoma; clinical surgical biopsy or stereotactic biopsy has been performed to obtain clear histopathological diagnosis; not feasible to re-contact patients; patients who sought medical care at Southern Hospital of Southern Medical University between January 2000 and December 2023.

Exclusion criteria

Exclusion criteria: 1.Secondary Central Nervous System Lymphoma: Patients diagnosed with systemic lymphoma with central nervous system metastasis; 2.Other Central Nervous System Malignancies: Non-lymphocytic tumors such as gliomas, meningiomas, and other tumors not of lymphocytic origin; 3.Severe Organ Dysfunction: Such as severe cardiovascular disease, hepatic insufficiency, renal insufficiency, or other diseases that may affect survival prognosis; 4.Concurrent Severe Infection or Other Acute Diseases: Diseases that affect patient participation in the study or study results; 5.Pregnant or Lactating Women; 6.Patients deemed unsuitable for participation in this study based on the investigator's judgment.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate, ORR;Progression-Free Survival, PFS;Overall Survival, OS;

Countries

China

Contacts

Public ContactHao Long

Southern Medical University Southern Hospital

longh812@163.com+86 20 6164 1806

Outcome results

None listed

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