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Hyper-CVAD Treatment in Lymphoblastic Lymphoma (LBL-CISL-1)

A

Ajou University School of Medicine

Status

Unknown

Conditions

Lymphoblastic Lymphoma

Study type

Observational

Funder types

Other

Identifiers

NCT01813344
LBL-CISL-1

Details and patient eligibility

About

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.

Full 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.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age over 18 at diagnosis
  • Pathologically proven lymphoblastic lymphoma

Exclusion criteria

  • proven HIV infection
  • pretreatment with other regimens

Trial contacts and locations

1

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Central trial contact

Seong Hyun Jeong, MD

Data sourced from clinicaltrials.gov

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