German Multicenter Trial for the Treatment of Newly Diagnosed T-lymphoblastic Lymphoma in Adults

NCT00199017 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2010-08-23

No results posted yet for this study

Summary

This study evaluates the efficacy and tolerability of treatment for T-lymphoblastic lymphoma (T-LBL) according to a protocol for acute lymphoblastic leukemia. Patients receive one year of intensive cyclical chemotherapy with additional prophylaxis for central nervous system (CNS) relapse by intrathecal therapy and cranial irradiation and mediastinal irradiation after induction chemotherapy.

Conditions

  • Lymphoma, Lymphoblastic

Interventions

DRUG

Dexamethasone/Prednisolone

DRUG

Vincristine

DRUG

Daunorubicin

DRUG

Asparaginase

DRUG

G-CSF

DRUG

Mercaptopurine

DRUG

Cytarabine

DRUG

Methotrexate

DRUG

VP16

DRUG

Vindesine

DRUG

Adriamycin

DRUG

Thioguanine

DRUG

HDARAC

PROCEDURE

CNS irradiation

PROCEDURE

Mediastinal irradiation

DRUG

Cladribine

Sponsors & Collaborators

  • Johann Wolfgang Goethe University Hospital

    lead OTHER

Principal Investigators

  • Dieter Hoelzer, MD, PhD · University Hospital Frankfurt, Medical Dept. II

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
15 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-04-30
Primary Completion
2009-03-31

Countries

  • Germany

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00199017 on ClinicalTrials.gov