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Spots Global Cancer Trial Database for Hyper-CVAD Treatment in Lymphoblastic Lymphoma

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Trial Identification

Brief Title: Hyper-CVAD Treatment in Lymphoblastic Lymphoma

Official Title: The Clinical Outcomes of Hyper-CVAD Treatment in Lymphoblastic Lymphoma

Study ID: NCT01813344

Interventions

Study Description

Brief Summary: 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.

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Ajou Universtiy School of Medicine, Suwon, Kyeonggi, Korea, Republic of

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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