Skip to main content
Clinical Trials/NCT05635435
NCT05635435
Recruiting
Not Applicable

Preoperative Immune and Inflammatory Indices in Peripheral Blood Predict Prognosis of Glioma and Correlate With Grades and Subtypes: A Prospective Multi-Institutional Study

Sun Yat-sen University3 sites in 1 country1,282 target enrollmentOctober 13, 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Glioma
Sponsor
Sun Yat-sen University
Enrollment
1282
Locations
3
Primary Endpoint
all-cause mortality
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

Our study considered the relevant immune and inflammatory indices, such as immunoglobulin kappa light chain, TNF, and CD4+ Helper T lymphocyte% in a multi-institutional study with a large patient cohort (n=1282) from the east, northeast, and southeast of China. Our study shed light on the association of peripheral immune system status with prognosis, tumor grade, and subtype of glioma, which can potentially benefit future diagnostic and prognostic processes of glioma given its noninvasive nature. Moreover, the preoperative inflammatory status can be leveraged for timely interventions to reverse the immunosuppressive status of cancer patients and enhance anti-tumour immunity of glioma.

Registry
clinicaltrials.gov
Start Date
October 13, 2006
End Date
December 20, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Sun Yat-sen University
Responsible Party
Principal Investigator
Principal Investigator

Yonggao Mou

Clinical Professor

Sun Yat-sen University

Eligibility Criteria

Inclusion Criteria

  • glioma grading and classification histologically verified in a resection or biopsy specimen according to 2016 WHO criteria;
  • age \> 18 years;
  • primary malignant glioma;
  • the duration of follow-up \> 3 months;
  • available data of lymphocyte subsets, cytokines, immune proteins and immune complements measured at the patient's first hospitalization.
  • Exculsion Criteria:
  • current infectious disease, hyperpyrexia, hematological disease, diabetes mellitus, serious heart disease, hypertension, metabolic syndrome, severe renal or hepatic dysfunction, other cancer, autoimmune disease, inflammatory disease, or medication usage related to an inflammatory condition;
  • prior cancer-specific pretreatment, such as chemotherapy or radiotherapy;

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

all-cause mortality

Time Frame: 16 years

For this study, the endpoint was all-cause mortality. Time zero was set at the time of resection of the primary tumor.

Study Sites (3)

Loading locations...

Similar Trials