Hyper-CVAD Treatment in Lymphoblastic Lymphoma (LBL-CISL-1)
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ClinicalTrials.gov Identifier: NCT01813344
Recruitment Status : Unknown
Verified March 2013 by Seong Hyun Jeong, Ajou University School of Medicine. Recruitment status was: Recruiting
First Posted : March 19, 2013
Last Update Posted : March 19, 2013
Ajou University School of Medicine
Information provided by (Responsible Party):
Seong Hyun Jeong, Ajou University School of Medicine
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.
Condition or disease
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.
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Ages Eligible for Study:
18 Years and older (Adult, Older Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Adult lymphoblast lymphoma patients treated with hyper-CVAD regimen in Korea