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Randomized Phase III Trial Evaluating the Role of Autologous Stem Cell Transplantation in Previously Untreated Patients With Stage B and C Chronic Lymphocytic Leukemia


Phase 3
18 Years
65 Years
Not Enrolling
Both
Chronic Lymphocytic Leukemia

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Trial Information

Randomized Phase III Trial Evaluating the Role of Autologous Stem Cell Transplantation in Previously Untreated Patients With Stage B and C Chronic Lymphocytic Leukemia


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).


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

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Progression free survival

Outcome Time Frame:

3 year

Safety Issue:

Yes

Principal Investigator

Sutton Laurent, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Hospital Victor Dupouy Argenteuil, France

Authority:

France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)

Study ID:

SFGMTC

NCT ID:

NCT00931645

Start Date:

April 2001

Completion Date:

December 2008

Related Keywords:

  • Chronic Lymphocytic Leukemia
  • Chronic lymphocytic leukemia,
  • autologous stem cell transplantation
  • Leukemia
  • Leukemia, Lymphocytic, Chronic, B-Cell
  • Leukemia, Lymphoid

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