Prognostic Nomogram of Extranodal NK/T-cell Lymphoma
1 other identifier
observational
1,000
1 country
1
Brief Summary
This study aims to evaluate prognostic factors for overall survival and explore risk progression-free survival in ENKTL, and establish a prognostic predictive nomogram for ENKTL patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2020
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 28, 2020
CompletedFirst Submitted
Initial submission to the registry
September 12, 2020
CompletedFirst Posted
Study publicly available on registry
September 18, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2024
CompletedJune 18, 2023
June 1, 2023
3.3 years
September 12, 2020
June 15, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Overall survival
Time between the date of diagnosis and any kinds of death
5 year
Secondary Outcomes (1)
Progression-free survival
5 year
Study Arms (2)
Training cohort
Patients diagnosed with ENKTL, between January 1, 2000 and August 31, 2020.
Validation Cohort
Patients diagnosed with ENKTL, between January 1, 2000 and August 31, 2020.
Eligibility Criteria
1. Patients diagnosed with ENKTL, between January 1, 2000 and August 31, 2020; 2. Patients older than 18 years.
You may qualify if:
- Patients newly diagnosed with ENKTL
- Patients diagnosed between January 1, 2000 and August 31, 2020
- Patients older than 18 years
You may not qualify if:
- Patients who did not have complete clinical information or immunohistochemistry, or who were lost follow-up immediately after treatment.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sun Yat-sen University Cancer Center
Guangzhou, Guangdong, 510060, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Hua Wang
Sun Yat-sen University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- associate chief physician
Study Record Dates
First Submitted
September 12, 2020
First Posted
September 18, 2020
Study Start
August 28, 2020
Primary Completion
January 1, 2024
Study Completion
January 1, 2024
Last Updated
June 18, 2023
Record last verified: 2023-06