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Clinical Trials/NCT03051555
NCT03051555
Unknown
Not Applicable

18F-FDG PET/CT-based Prognostic Model for Predicting Outcome in Patients With Natural Killer/T-cell Lymphoma

Peking University Cancer Hospital & Institute1 site in 1 country60 target enrollmentMarch 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lymphoma, Extranodal NK-T-Cell
Sponsor
Peking University Cancer Hospital & Institute
Enrollment
60
Locations
1
Primary Endpoint
3 year progression-free survival
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to evaluate whether 18F-FDG PET/CT-based prognostic model of NK/T-cell lymphoma can predict disease progression

Detailed Description

In this study investigators develop a prognostic model based on 18F-FDG PET/CT and test its ability for prognostic value in patients with DLBCL. PET/ CT scans evaluation using the liver SUVmax as reference. Positive lesions in PET were indicated as SUVmax of residues higher than the threshold or new 18F-FDG avid lesions. 18F-FDG PET/CT-based prognostic model includes PET/CT image, dominant clinical and pathological prognostic factors to predicting disease progression during chemotherapy or survival in NK/T-cell lymphoma.

Registry
clinicaltrials.gov
Start Date
March 1, 2017
End Date
December 31, 2020
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Peking University Cancer Hospital & Institute
Responsible Party
Principal Investigator
Principal Investigator

Xuejuan Wang,MD

Principal Investigator

Peking University Cancer Hospital & Institute

Eligibility Criteria

Inclusion Criteria

  • newly diagnosed NK/T-cell lymphoma
  • treated using an anthracycline-containing regimen
  • minimal follow-up at 6 months after the completion of first-line treatment
  • complete medical history and clinicopathological data

Exclusion Criteria

  • secondary malignant disease
  • serious infection or inflammation (e.g., HIV)
  • primary central nervous system lymphoma
  • hepatic or renal dysfunction.

Outcomes

Primary Outcomes

3 year progression-free survival

Time Frame: up to 3 years after initial diagnosis

Study Sites (1)

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