- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01813344
Hyper-CVAD Treatment in Lymphoblastic Lymphoma (LBL-CISL-1)
March 14, 2013 updated by: Seong Hyun Jeong, Ajou University School of Medicine
The Clinical Outcomes of Hyper-CVAD Treatment in Lymphoblastic Lymphoma
Treatment outcomes of lymphoblastic lymphoma (LBL) have improved by the use of the regimens for acute lymphoblastic leukemia.
Hyper-CVAD is one of the most effective treatments with high remission rate in acute lymphoblastic leukemia (ALL) and LBL.
However, the treatment outcome of hyper-CVAD in LBL has reported only in small number of patients from single institution.
The investigators conducted this study to evaluate the hyper-CVAD regimen based treatment in LBL.
Study Overview
Status
Unknown
Conditions
Detailed Description
We will analyze treatment outcome of lymphoblastic lymphoma patients treated with hyper-CVAD regimen from 13 institutions in Korea.
In all patients, hyper-CVAD was initial treatment.
After achievement of response, patients either underwent hematopoietic stem cell transplantation (HSCT) or consolidation with hyper-CVAD.
Study Type
Observational
Enrollment (Anticipated)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Seong Hyun Jeong, MD
- Phone Number: +82-31-219-5989
- Email: seonghyunmd@naver.com
Study Locations
-
-
Kyeonggi
-
Suwon, Kyeonggi, Korea, Republic of, 443-721
- Recruiting
- Ajou Universtiy School of Medicine
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Adult lymphoblast lymphoma patients treated with hyper-CVAD regimen in Korea
Description
Inclusion Criteria:
- age over 18 at diagnosis
- Pathologically proven lymphoblastic lymphoma
Exclusion Criteria:
- proven HIV infection
- pretreatment with other regimens
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Overall survival
Time Frame: 3-year
|
3-year
|
Progression free survival
Time Frame: 3-year
|
3-year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Response Rate
Time Frame: 24 weeks
|
24 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2012
Primary Completion (ANTICIPATED)
June 1, 2013
Study Registration Dates
First Submitted
March 13, 2013
First Submitted That Met QC Criteria
March 14, 2013
First Posted (ESTIMATE)
March 19, 2013
Study Record Updates
Last Update Posted (ESTIMATE)
March 19, 2013
Last Update Submitted That Met QC Criteria
March 14, 2013
Last Verified
March 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- LBL-CISL-1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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