search
Back to results

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

Primary Purpose

Lymphoma, Large B-Cell, Diffuse

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
18F-FDG PET/CT
Sponsored by
Peking University Cancer Hospital & Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Lymphoma, Large B-Cell, Diffuse focused on measuring Positron-Emission Tomography, Prognosis

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. newly diagnosed DLBCL;
  2. treated using an anthracycline-containing regimen with or without rituximab;
  3. minimal follow-up at 6 months after the completion of first-line treatment;
  4. complete medical history and clinicopathological data

Exclusion Criteria:

  1. secondary malignant disease;
  2. serious infection or inflammation (e.g., HIV);
  3. primary central nervous system lymphoma;
  4. hepatic or renal dysfunction.

Sites / Locations

  • Peking University Cancer HospitalRecruiting
  • Peking University Cancer HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

18F-FDG PET/CT-based prognostic model

Arm Description

The new prognostic model is based on 18F-FDG PET/CT scans, and combined with clinical and pathological prognostic factors.

Outcomes

Primary Outcome Measures

2 year progression-free survival

Secondary Outcome Measures

Full Information

First Posted
October 7, 2016
Last Updated
October 7, 2016
Sponsor
Peking University Cancer Hospital & Institute
search

1. Study Identification

Unique Protocol Identification Number
NCT02928861
Brief Title
18F-FDG PET/CT-based Prognostic Model for Predicting Outcome in Patients With Diffuse Large B-cell Lymphoma
Official Title
18F-FDG PET/CT-based Prognostic Model for Predicting Outcome in Patients With Diffuse Large B-cell Lymphoma
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Unknown status
Study Start Date
October 2016 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University Cancer Hospital & Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphoma, Large B-Cell, Diffuse
Keywords
Positron-Emission Tomography, Prognosis

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
18F-FDG PET/CT-based prognostic model
Arm Type
Experimental
Arm Description
The new prognostic model is based on 18F-FDG PET/CT scans, and combined with clinical and pathological prognostic factors.
Intervention Type
Device
Intervention Name(s)
18F-FDG PET/CT
Intervention Description
18F-FDG PET/CT will be conducted before, during and after chemotherapy. Patients were instructed to fast for at least 6 h before PET. The blood glucose level was measured to ensure that it was <200 mg/ dL. 18F-FDG was intravenously administered at a dose of 3.7 MBq/kg. Approximately 60 ± 10 min post- injection, a whole-body acquisition commenced in 6-8 bed positions (1 min/bed) using a hybrid system (PHILIPS Gemini TF) and covered from the base of the skull to the upper thigh, which was followed by CT in a non-contrast phase (modulated 100 mAs; 120 kV; slice thickness, 3 mm) for attenuation correction and anatomical localization purposes. The head acquisition was performed in one bed position (8-10 min/bed).
Primary Outcome Measure Information:
Title
2 year progression-free survival
Time Frame
up to 2 years after initial diagnosis

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xuejuan Wang, MD
Phone
86 10-88196364
Email
xuejuan_wang@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xuejuan Wang, MD
Organizational Affiliation
Peking University Cancer Hospital & Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking University Cancer Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100142
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xuejuan Wang, MD
Phone
86 10-88196364
Email
xuejuan_wang@hotmail.com
First Name & Middle Initial & Last Name & Degree
Yuewei Zhang
Email
zhang_yue_wei@126.com
Facility Name
Peking University Cancer Hospital
City
Beijing
ZIP/Postal Code
100142
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xuejuan Wang, MD
Phone
86 10-88196364
Email
xuejuan_wang@hotmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35530320
Citation
Yuan T, Zhang Y, Chen X, Wei M, Zhu H, Song Y, Yang Z, Zhu J, Wang X. Risk Assessment in Diffuse Large B-Cell Lymphoma by Combining Baseline Metabolic Tumor Volume and Peking Criteria When Evaluating Series 18F-Fluorodeoxyglucose Positron Emission Tomography Scans. Front Oncol. 2022 Apr 21;12:876581. doi: 10.3389/fonc.2022.876581. eCollection 2022.
Results Reference
derived

Learn more about this trial

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

We'll reach out to this number within 24 hrs