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A multicentric prospective prognostic cohort with epidemiological, clinical, biological and treatment information to improve knowledge on lymphoma patients

A multicentric prospective prognostic cohort with epidemiological, clinical, biological and treatment information to improve knowledge on lymphoma patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0008870
Enrollment
2000
Registered
2023-10-16
Start date
2023-06-08
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

None listed

Interventions

None listed

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with the following lymphoid malignancies through histopathological diagnostic procedures, regardless of whether they were previously treated: 1) Hodgkin lymphoma 2) B-cell non-Hodgkin lymphoma 3) T or NK cell non-Hodgkin lymphoma 4) Diseases included in the category of lymphoid malignancies in other WHO classifications 2. Patients over 20 years of age 3. Patients who gave written consent to participate in a prospective cohort study

Exclusion criteria

Exclusion criteria: 1. In case of malignant tumor of the lymphatic system that falls under any of the following diseases: yes; Plasma cell disease, amyloidosis 2. If you are a patient with the following lymphatic malignancies: 1) In case of follow-up observation after diagnosis because treatment is not necessary 2) When only local radiation therapy is planned for the purpose of anticancer treatment 3) When using only antiviral drugs, antibiotics, or steroids rather than anticancer drugs for the purpose of anticancer treatment 3. Patients who do not understand or do not agree to written consent

Design outcomes

Primary

MeasureTime frame
Factors associated with treatment response and survival (Response rate to first-line treatment administered after registration, Response rate to rescue treatment administered after disease recurrence or progression, overall survival rate, Progression-free survival)

Secondary

MeasureTime frame
Serious adverse events and serious and unexpected adverse drug events

Countries

Korea, Republic of

Contacts

Public Contactdanbee Kang

Samsung Medical Center

dbee.kang@gmail.com+82-2-3410-1766

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026