Prospective Cohort Study for Lymphoma: Samsung Lymphoma Cohort Study IV

ConditionLymphoma
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorSamsung Medical Center

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Pathologically diagnosed Hodgkin and non-Hodgkin lymphomas

20 years

Patients requiring systemic chemotherapy with curative intent

Written informed consent

Disqualifiers

Myeloid malignancy

Multiple myeloma

Patients do not require systemic chemotherapy with curative intent

Trial population

Patients are diagnosed with aggressive lymphoma including Hodgkin and non-Hodgkin lymphoma. All patients should receive systemic chemotherapy. Newly diagnosed or relapsed/refractory patients can be enrolled

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Immunochemotherapy

    Drug

    Systemic chemotherapy with curative intent

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Reponse rate

Repsonse to the ist line treatment

Time frame
3 months after the completion of treatment
2

Response

response to treatment

Time frame
3 months after chemotherapy

Secondary outcomes

Other outcomes

Sponsors and contacts

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