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临床试验/NCT04317313
NCT04317313已完成不适用

Synergistic Effect of 18F-FDG PET Radiomics and International Prognostic Index on Outcome Prediction in Diffuse Large B-cell Lymphoma

Second Affiliated Hospital, School of Medicine, Zhejiang University1 个研究点 分布在 1 个国家目标入组 152 人开始时间: 2020年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
152
试验地点
1
主要终点
Overall Survival

研究概览

简要总结

This study aims to investigate the prognostic value of 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET) radiomics in diffuse large B-cell lymphoma (DLBCL) and its additional value to the International Prognostic Index (IPI).

详细描述

Several studies have shown that 18F-FDG PET radiomics is predictive of survival in DLBCL. However, to the best of the investigator's knowledge, a multi-feature radiomic signature for prognosis assessment of DLBCL has not yet been described. Furthermore, it remains unclear whether PET-based radiomics could add more prognostic values to the IPI in DLBCL.

This study aims to develop 18F-FDG PET radiomic signature, and investigate whether the radiomic signature could improve the prognostic value of the IPI score in predicting progression-free survival (PFS) and overall survival (OS) in DLBCL.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • histopathologically confirmed diffuse large B-cell lymphoma (DLBCL);
  • Over 18 years old when diagnosed;
  • Have undergone pre-treatment 18F-FDG PET/CT;
  • Have been initially treated with the combination of rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP) or R-EPOCH (etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin).

排除标准

  • Have primary central nervous system (CNS) lymphoma or second primary cancer;
  • Have undergone surgical resection;
  • With an incomplete follow-up.

结局指标

主要结局

Overall Survival

时间窗: From date of the initial diagnosis until the date of death from any cause, whichever came first, up to 8 years

the period from the initial diagnosis to the death from any cause

Progression-free Survival

时间窗: From date of the initial diagnosis until the date of first documented progression, relapse or death from any cause, whichever came first, up to 8 years

the period from the initial diagnosis to the progression, relapse or death from any cause

次要结局

未报告次要终点

研究者

发起方
Second Affiliated Hospital, School of Medicine, Zhejiang University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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