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Clinical Trials/NCT02928861
NCT02928861
Unknown
Not Applicable

18F-FDG PET/CT-based Prognostic Model for Predicting Outcome in Patients With Diffuse Large B-cell Lymphoma

Peking University Cancer Hospital & Institute1 site in 1 country100 target enrollmentOctober 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lymphoma, Large B-Cell, Diffuse
Sponsor
Peking University Cancer Hospital & Institute
Enrollment
100
Locations
1
Primary Endpoint
2 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 diffuse large B-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 (1.6 fold of liver SUVmax) 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 DLBCL.

Registry
clinicaltrials.gov
Start Date
October 2016
End Date
December 2018
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

Department of Nuclear Medicine

Peking University Cancer Hospital & Institute

Eligibility Criteria

Inclusion Criteria

  • newly diagnosed DLBCL;
  • treated using an anthracycline-containing regimen with or without rituximab;
  • 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

2 year progression-free survival

Time Frame: up to 2 years after initial diagnosis

Study Sites (1)

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