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Fludarabine or Observation in Treating Patients With Stage 0, Stage I, or Stage II Chronic Lymphocytic Leukemia

Prognostic Factors and Risk-Adapted Therapy in Patients With Early Stage Chronic Lymphocytic Leukemia

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00262782
Enrollment
877
Registered
2005-12-07
Start date
1997-04-30
Completion date
2010-06-30
Last updated
2020-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Lymphocytic Leukemia

Keywords

B-cell chronic lymphocytic leukemia, stage 0 chronic lymphocytic leukemia, stage I chronic lymphocytic leukemia, stage II chronic lymphocytic leukemia

Brief summary

RATIONALE: Drugs used in chemotherapy, such as fludarabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Sometimes, the cancer may not need treatment until it progresses. In this case, observation may be sufficient. It is not yet known whether fludarabine is more effective than observation in treating chronic lymphocytic leukemia. PURPOSE: This randomized phase III trial is studying fludarabine to see how well it works compared to observation only in treating patients with stage 0, stage I, or stage II B-cell chronic lymphocytic leukemia.

Detailed description

OBJECTIVES: * Identify prognostic factors that predict a short survival in patients with stage 0-II B-cell chronic lymphocytic leukemia treated with fludarabine or observation only. OUTLINE: This is a randomized study. Patients are stratified according to risk (high risk vs low risk). Patients in the low-risk group undergo observation only. Patients in the high-risk group are randomized to 1 of 2 treatment arms. * Arm I: Patients receive fludarabine. * Arm II: Patients undergo observation only. PROJECTED ACCRUAL: A total of 880 patients will be accrued for this study.

Interventions

DRUGFludarabine

Fludarabine i.v. (25 mg/m2/d, d1-5) q28d; max 6 cycles

Sponsors

German CLL Study Group
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Confirmed diagnosis of B-cell chronic lymphocytic leukemia * Rai stage 0-II (Binet stage A) disease * Meets 1 of the following criteria: * High-risk disease, as defined by the following: * Serum thymidine kinase level \> 7.0 U/L * Elevated β2-microglobulin level * Presence of non-nodular bone marrow infiltration * Short lymphocyte doubling time * Low-risk disease * Meets none of the criteria (as listed above) for high-risk disease PATIENT CHARACTERISTICS: Performance status * Not specified Life expectancy * More than 6 months Hematopoietic * No autoimmune hemolytic anemia * No thrombocytopenia Hepatic * Not specified Renal * Not specified Other * No severe organ dysfunction * No other prior or concurrent malignancy PRIOR CONCURRENT THERAPY: Chemotherapy * No prior chemotherapy * No other concurrent chemotherapy

Countries

Austria, Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026