- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04554511
Prognostic Nomogram of Extranodal NK/T-cell Lymphoma
June 15, 2023 updated by: Hua Wang, Sun Yat-sen University
Prognostic Nomogram of Extranodal NK/T-cell Lymphoma: A Multi-center Retrospective Study
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.
Study Overview
Status
Recruiting
Conditions
Detailed Description
This is a retrospective cohort study using anonymized information from patients with ENKTL.
The following criteria are required: (1) Patients diagnosed with ENKTL between January 1, 2000 and August 31, 2020; (2) Patients older than 18 years.
The pathology of initial diagnosis was reviewed by designated pathologists.
Study Type
Observational
Enrollment (Estimated)
1000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Hua Wang
- Phone Number: +862087342462
- Email: wanghua@sysucc.org.cn
Study Locations
-
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Guangdong
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Guangzhou, Guangdong, China, 510060
- Recruiting
- Sun Yat-Sen University Cancer Center
-
Contact:
- hua wang, MD.
- Phone Number: 0086-02087342462
- Email: wanghua@sysucc.org.cn
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
- Patients diagnosed with ENKTL, between January 1, 2000 and August 31, 2020;
- Patients older than 18 years.
Description
Inclusion Criteria:
- Patients newly diagnosed with ENKTL
- Patients diagnosed between January 1, 2000 and August 31, 2020
- Patients older than 18 years
Exclusion Criteria:
- Patients who did not have complete clinical information or immunohistochemistry, or who were lost follow-up immediately after treatment.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Overall survival
Time Frame: 5 year
|
Time between the date of diagnosis and any kinds of death
|
5 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Progression-free survival
Time Frame: 5 year
|
Time between the date of diagnosis and any kinds of death or relapse/progression
|
5 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Hua Wang, Sun Yat-sen University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 28, 2020
Primary Completion (Estimated)
January 1, 2024
Study Completion (Estimated)
January 1, 2024
Study Registration Dates
First Submitted
September 12, 2020
First Submitted That Met QC Criteria
September 12, 2020
First Posted (Actual)
September 18, 2020
Study Record Updates
Last Update Posted (Estimated)
June 16, 2023
Last Update Submitted That Met QC Criteria
June 15, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ENKTL-2020
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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