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Prospective Cohort Study for Lymphoma: Samsung Lymphoma Cohort Study IV

A Prospective Study for Patients With Lymphoma at the Samsung Medical Center

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07032103
Acronym
SMCLYM-IV
Enrollment
2000
Registered
2025-06-22
Start date
2022-06-01
Completion date
2028-12-30
Last updated
2025-06-22

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

Conditions

Lymphoma

Keywords

lymphoma, prognosis

Brief summary

This prospective study enrolls patients who are diagnosed with aggressive lymphoma including Hodgkin and non-Hodgkin lymphomas. Enrolled patients will be treated according to our institution' treatment policy in clinical practice. The disease status including response to therapy and survival status will be regularly updated during the study period. Patients' serum and cell-free DNA will be collected and analyzed.

Detailed description

The study population is aggressive lymphomas requiring systemic chemotherapy. Newly diagnosed or relapsed/refractory patients can be enrolled into the study. Patients can be treated according to the principle of routine care of our institute. The study process is as follows. 1. Registration after informed consent. 2. Laboratory and radiological evaluation after registration including collection of serum and cell-free DNA from patients' peripheral blood 3. Interim and final response evaluation including collection of serum and cell-free DNA from patients' peripheral blood 4. Regular monitoring disease status and update of survival status 5. Laboratory and radiological evaluation after relapse or progression including collection of serum and cell-free DNA from patients' peripheral blood

Interventions

Systemic chemotherapy with curative intent

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Pathologically diagnosed Hodgkin and non-Hodgkin lymphomas 2. 20 years 3. Patients requiring systemic chemotherapy with curative intent 4. Written informed consent

Exclusion criteria

1. Myeloid malignancy 2. Multiple myeloma 3. Patients do not require systemic chemotherapy with curative intent

Design outcomes

Primary

MeasureTime frameDescription
Reponse rate3 months after the completion of treatmentRepsonse to the ist line treatment
Response3 months after chemotherapyresponse to treatment

Countries

South Korea

Contacts

Primary ContactSeok Jin Kim, MD., PhD.
kstwoh@gmail.com+82234101766

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026