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A Multicentric Phase III Study in Patients With CLL B and C < 60 Years Not Treated: 6 Montly CHOP + 6 CHOP Every 3 Months Versus 3 Montly CHOP + Intensification and Autograft


Phase 3
18 Years
60 Years
Not Enrolling
Both
Leukemia, Lymphocytic, Chronic

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Trial Information

A Multicentric Phase III Study in Patients With CLL B and C < 60 Years Not Treated: 6 Montly CHOP + 6 CHOP Every 3 Months Versus 3 Montly CHOP + Intensification and Autograft


The aim of the prospective randomized GOELAMS LLC 98 trial reported here was to compare two
therapeutic strategies in previously untreated B and C Binet stages B-CLL patients less than
60 years old. Conventional chemotherapy (Arm A) consisted of six monthly courses of CHOP,
i.e. vincristin IV 1 mg/m2 on day 1, doxorubicin IV 25 mg/m2 on day 1, cyclophosphamide (Cy)
300 mg/m2 and prednisone 40 mg/m2 both given orally from day 1 to day 5, followed by 6 CHOP
courses every other 3 months in case of response. Fludarabine (25 mg/m2 /d IV for 5
consecutive days) was used in case of non response (stable disease or progression) after 3
CHOP courses. This conventional therapy was compared to high dose therapy with autologous
CD34+ purified progenitor cell support (Arm B), used as consolidation of Complete Remission
(CR) or Very Good Partial Response (VGPR, defined by >50 % tumoral response and bone marrow
lymphocyte infiltration <30%) obtained after 3 monthly courses of CHOP. In the absence of CR
or VGPR, 3 to 6 monthly-courses of fludarabine were performed before mobilization with Cy 4
g/m2 + G-CSF administration. The conditioning regimen included TBI 12 Gy and Cy 60 mg /kg /d
for 2 days.


Inclusion Criteria:



- CLL with Lymphocitis > 15.10 9/L

- B-CLL stage B or C

- Patients > 18 years old and < 60 years old

- No previous treatment of CLL

- ECOG performance status < 2

- Good cardiac function

- Patient's written informed consent

Exclusion Criteria:

- B-CLL stage A

- Age > 60 years old

- previous treatment of CLL

- ECOG performance status > 2

- Cardiac or pneumo Insufficency

- hepatic or renal Insufficency

- Seropositivity HIV

- Previous other malignancy

- Fertile male and female patients who cannot or do not wish to use an effective method
of contraception

- Any coexisting medical or psychological condition that would preclude participation
to the required study procedures

- NOt signed Patient's informed consent

Type of Study:

Interventional

Study Design:

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

Outcome Measure:

progression free survival

Outcome Time Frame:

Overal survival

Principal Investigator

Annie BRION, RN

Investigator Role:

Principal Investigator

Investigator Affiliation:

Groupe Ouest Est d'Etude des Leucémies et Autres Maladies du Sang GOELAMS

Authority:

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

Study ID:

LLC 98

NCT ID:

NCT00535912

Start Date:

January 1999

Completion Date:

March 2006

Related Keywords:

  • Leukemia, Lymphocytic, Chronic
  • CLL
  • Leukemia
  • Leukemia, Lymphocytic, Chronic, B-Cell
  • Leukemia, Lymphoid

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