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Cohort of Peripheral T Cell Lymphoma

Multicenter Prospective Cohort Study of Peripheral T Cell Lymphoma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02364466
Enrollment
200
Registered
2015-02-18
Start date
2015-01-31
Completion date
2019-12-31
Last updated
2015-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Febrile Neutropenia, Lymphoma, T-Cell, Peripheral

Brief summary

Prospective, observational cohort study of peripheral T cell lymphoma. Purpose is to investigate the complication including febrile neutropenia in the era of pegylated G-CSF prophylaxis.

Detailed description

Prospective evaluation of frequencies of febrile neutropenia or infectious complications in a homogeneous population of patients with peripheral T cell lymphoma

Interventions

None listed

Sponsors

Samsung Medical Center
CollaboratorOTHER
Asan Medical Center
CollaboratorOTHER
Keimyung University Dongsan Medical Center
CollaboratorOTHER
Kosin University Gospel Hospital
CollaboratorOTHER
Dankook University
CollaboratorOTHER
Soonchunhyang University Hospital
CollaboratorOTHER
Ajou University School of Medicine
CollaboratorOTHER
Yeungnam University Hospital
CollaboratorOTHER
Ulsan University Hospital
CollaboratorOTHER
Inje University
CollaboratorOTHER
Chung-Ang University Hosptial, Chung-Ang University College of Medicine
CollaboratorOTHER
Hallym University Medical Center
CollaboratorOTHER
Hanyang University Seoul Hospital
CollaboratorOTHER
Seoul National University Hospital
CollaboratorOTHER
Pusan National University Hospital
CollaboratorOTHER
National Health Insurance Service Ilsan Hospital
CollaboratorOTHER
Hanyang University
CollaboratorOTHER
Korea Cancer Center Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Treatment naive peripheral T cell lymphoma Subtypes are as followings: Anaplastic large cell lymphoma angioimmunoblastic T cell lymphoma Peripheral T cell lymphoma-NOS Enteropathy-associated T cell lymphoma Hepatosplenic T-cell lymphoma Subcutaneous panniculitis-like T-cell lymphoma Primary cutaneous gamma-delta T-cell lymphoma Primary cutaneous CD8+ aggressive epidermotropic lymphoma 2. Scheduled to receive chemotherapy of curative intent 3. 19 years old or over 4. Expected survival is more than 6 months 5. Informed consent

Exclusion criteria

1. Other histology than those described above * Extranodal NK/T cell lymphoma * Other than peripheral T cell lymphoma 2. Other combined malignancy 3. Previous history of chemotherapy or radiation therapy 4. No informed consent

Design outcomes

Primary

MeasureTime frameDescription
Febrile neutropenia2 years after the last enrollmentIncidence and severity of febrile neutropenia

Secondary

MeasureTime frameDescription
Infectious complication2 years after the last enrollmentincidence, severity, microbiology of infection

Countries

South Korea

Contacts

Primary ContactDong-Yeop Shin, M.D.
baramg@hanmail.net+82-2-970-1246

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026