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Samsung Medical Center-Lymphoma Cohort Study

Development of a Predictive Model for Treatment Outcome and Treatment-related Morbidity in a Prospective Cohort Study of Patients With Lymphoma

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00822731
Acronym
SMC-LCS
Enrollment
953
Registered
2009-01-14
Start date
2008-09-30
Completion date
2011-12-31
Last updated
2012-05-23

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

Conditions

Lymphoma

Keywords

Lymphoma, prognosis, morbidity

Brief summary

The purpose of this study is to establish a model which can predict the treatment outcome and the risk of treatment-related morbidity in patients with lymphoma.

Detailed description

Although the cure rate of lymphoma has been increased due to the development of newer effective drugs, a substantial portion of patients is still suffered from relapse. Furthermore, the treatment-related morbidity is another factor which can make the treatment outcome worse in patients with lymphoma, especially elderly patients. Thus, this study is going to assess following factors which amy probably affect the treatment outcome and the risk of treatment-related morbidity. 1. Biologic factors associated with the aggressiveness of lymphoma * molecular markers in serum, cytogenetic markers 2. Factors associated with the risk of treatment-related morbidity * comorbidity, nutrition status, performance status, quality of life at diagnosis

Interventions

DRUGChemotherapy with or without radiotherapy

Treatment regimen will be determined by the sub-type of lymphoma

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

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

Inclusion criteria

* Patients who were diagnosed as lymphoma * Over 15 years old * Patients who agreed the enrollment of study * Informed consent for sampling

Exclusion criteria

* Patients who do not want to join the study

Design outcomes

Primary

MeasureTime frame
all cause mortality5 years

Secondary

MeasureTime frame
Treatment responseafter completion of primary therapy
Rate of occurrence of toxicity2 years from the start of the 1st therapy
Treatment-related morbiditywithin 60 days from the previous therapy

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026