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Risk Stratification of Nodal PTCL

C

Chonbuk National University

Status

Completed

Conditions

Angioimmunoblastic T-cell Lymphoma
Anaplastic Large Cell Lymphoma, ALK-negative
Peripheral T-Cell Lymphoma, Not Otherwise Specified

Study type

Observational

Funder types

Other

Identifiers

NCT03040206
nodal PTCL

Details and patient eligibility

About

This study is to investigate the prognostic significance of enhanced International Prognostic Index (NCCN-IPI) and post-treatment PET results in patients with newly diagnosed nodal peripheral T-cell lymphoma (PTCL), and establish a risk stratification model for nodal PTCL patients.

Enrollment

405 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients diagnosed with nodal PTCLs (PTCL, NOS; Angioimmunblastic T-cell lymphoma; anaplastic large cell lymphoma [ALCL], anaplastic lymphoma kinase [ALK]-negative)
  • Patients diagnosed with between January 1, 2004 and April 30, 2016
  • initially treated with curative intent
  • Patients with standard 18F-fluorodeoxyglucose (FDG) PET or PET-CT data at the time of diagnosis and at the end of primary treatment

Exclusion criteria

  • Patients diagnosed with extranodal PTCLs, including followings (extranodal NK/T-cell lymphoma, nasal type; enteropathy-associated T-cell lymphoma; hepatosplenic T-cell lymphoma; subcutaneous panniculitis-like T-cell lymphoma; EBV-positive T-cell lymphoproliferative childhood disorders, and primary cutaneous lymphomas)
  • Patients with ALCL-ALK+
  • Patients who do not have 18F-FDG PET or PET-CT data either at diagnosis or at the end of treatment available for review

Trial design

405 participants in 1 patient group

Nodal PTCL
Description:
1. newly-diagnosed, pathologically-proven nodal PTCLs (PTCL, NOS; Angioimmunblastic T-cell lymphoma; anaplastic large cell lymphoma \[ALCL\], anaplastic lymphoma kinase \[ALK\]-negative) between January 1, 2005 and Jun 30, 2016 2. initially treated with curative intent 3. Standard PET or PET-CT data available at the time of diagnosis and at the end of primary treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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