Autologous Stem Cell Transplantation in Chronic Lymphocytic Leukemia (Auto-LLC 2001)

Caen University Hospital

Status and phase: Completed; Phase 3

Conditions: Chronic Lymphocytic Leukemia

Treatments: Procedure: Autologous stem cell transplantation; Procedure: DHAP rescue and F+C; Procedure: DHAP rescue and Autologous stem cell transplantation

Study type: Interventional

Funder types: Other

Identifiers

NCT00931645

PHRC

SFGMTC

Details and patient eligibility

About

Phase III trial evaluating the role of autologous stem cell transplantation in previously untreated patients under 65 years with stage B and C B-cell chronic lymphocytic leukemia.

Endpoints of the trial :

• major : progression free survival at 3 years
• secondary : overall survival, tolerance, prognostic factors according to baseline clinical stage and biological characteristics (IgHv mutational status, expression of ZAP70 and CD38, cytogenetics).

Full description

All registered patients will be treated with 6 monthly courses of chemotherapy. First three ones will be a CHOP regimen with half dosage of adriamycin, as previously published (Effectiveness of "CHOP" regimen in advanced untreated chronic lymphocytic leukemia. French Cooperative Group on Chronic Lymphocytic Leukemia. Lancet ; 1986, i : 1346-1349), followed by three subsequent courses with IV fludarabine (25 mg/sqm d1-5). Patients in CR (NCI, 1996, including CAT scan evaluation) will be then randomized to surveillance without additional treatment or autologous stem cell transplantation using peripheral stem cells collected after the three first courses of chemotherapy, and/or after the completion of the six courses when necessary. For patients not in CR after the six courses, a rescue regimen with the DHAP association ( cisplatin, 100 mg/sqm d1, cytarabine 2 g/sqm d2, dexamethasone 40 mg/sqm d1-4) will precede an additional stem cell collection if necessary, and patient will be randomized between autologous stem cell transplantation and three additional courses of an association of fludarabine (25 mg/sqm d1-3) and cyclophosphamide (300 mg/sqm d1-3). Conditioning regimen will associate TBI (10 grays, d -3-1) and cyclophosphamide (60 mg/sqm d-5-4).

Evaluation for response wil be performed before randomisation and two months after completion of therapy in each arm.

Follow-up data will be registered and monitored every three month during the first year, and then every six month. Criteria for evaluation of response will use the NCI system (1996).

Enrollment: 241 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• patients with stage B & C CLL, 18- 65 years.
• previously untreated
• given written informed consent

Exclusion criteria

• Childbearing women
• OMS Performance status > 2
• Binet stage A
• Autoimmune hemolytic anemia
• Active or previous (< 5 years) malignant disease, except cutaneous cell carcinoma.
• Previous CLL treatment
• HIV seropositivity
• Abnormal renal or liver function tests (creatinine > 1,5N, transaminases > 2N, bilirubin > 1,5N)
• Cardiac failure (ejection fraction < 50%)
• Lung disease or perturbed ventilation tests

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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241 participants in 4 patient groups

Complete responders

No Intervention group

Description:

watch and wait policy

arm 2: complete responders patients

Experimental group

Description:

ABMT : TBI, 10 grays d-3-1 \& cyclophosphamide 60 mg/sqm d-5-4

Treatment:

Procedure: Autologous stem cell transplantation

Non CR patients arm 3

Experimental group

Description:

Rescue chemotherapy and ABMT (see arm 2)

Treatment:

Procedure: DHAP rescue and Autologous stem cell transplantation

Non CR patients at random : arm 4

Active Comparator group

Description:

Rescue DHAP, F+C

Treatment:

Procedure: DHAP rescue and F+C