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Trial Comparing Chlorambucil to Fludarabine in Patients With Advanced Waldenström Macroglobulinemia
This study is currently recruiting participants.
Study NCT00566332   Information provided by French Study Group on Chronic Lymphoid Leukemia
First Received: November 30, 2007   No Changes Posted

November 30, 2007
November 30, 2007
June 2001
 
Patient overall response [ Time Frame: At the end of treatment whether 6 or 12 months ] [ Designated as safety issue: Yes ]
Same as current
No Changes Posted
  • Biological study [ Time Frame: Whether 6 or 12 months ] [ Designated as safety issue: No ]
  • Quality of life [ Time Frame: Whether 6 or 12 months ] [ Designated as safety issue: No ]
  • Response duration [ Time Frame: 60 months ] [ Designated as safety issue: Yes ]
  • Treatment toxicity [ Time Frame: 60 months ] [ Designated as safety issue: Yes ]
  • Event free survival [ Time Frame: 60 months ] [ Designated as safety issue: Yes ]
  • Overall survival [ Time Frame: 60 months ] [ Designated as safety issue: Yes ]
Same as current
 
Trial Comparing Chlorambucil to Fludarabine in Patients With Advanced Waldenström Macroglobulinemia
Randomized Trial Comparing the Efficacy of Chlorambucil to Fludarabine in Patients With Advanced Waldenström Macroglobulinemia,Lymphoplasmacytic Lymphoma or Splenic Marginal Zone Lymphoma

Waldenström's macroglobulinaemia (WM) is a lymphoproliferative disorder characterized by a monoclonal IgM paraprotein and morphological evidence of lymphoplasmacytic lymphoma: the cells are IgM+, IgD+, CD19+ and CD20+ but usually CD5-, CD10- and CD23-. The treatment efficacy is difficult to assess because of the lack of clear diagnostic criteria , good response criteria, and of randomized trials.

The actual treatment is Chlorambucil, an alkylating agent. A purine analogue such as Fludarabine has proven its efficacy on 30 % to 80 % as first line therapy

This study is a phase II b open, prospective, international multicenter trial (England, Dr Johnson, Dr Catovsky, Australia: Dr Seymour) promoted by the French Cooperative Group on Chronic Lymphoid Leukemia in untreated WM, or closely related disorders ( Lymphoplasmacytic lymphoma or splenic marginal zone lymphoma). 366 patients must be included, among them 180 patients in France. Patients will be stratified according to the lymphoproliferative disorder.

The patients will receive Chlorambucil by oral route for 10 days every 28 days (12 cycles) (8 MG/M², 6 MG/M² if patient is more than 75 years old) or Fludarabine by oral route for 5 days every 28 days (6 cycles) (40MG/M², 30 MG/M² if patient is more than 75 years old).

The primary objective is to compare the efficacy (response rate) of Chlorambucil to Fludarabine in previously untreated patients. The secondary objectives are the duration of response, the improvement of hematological parameters, the toxicity, the quality of life, the event free survival and the overall survival.

 
Phase III
Interventional
Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
  • Waldenström Macroglobulinemia
  • Lymphoplasmacytic Lymphoma
  • Splenic Marginal Zone Lymphoma
  • Drug: Chlorambucil
  • Drug: Fludarabine
  • Active Comparator: Chlorambucil 8mg/m² (6 mg/m² if patient aged more than 75 years old) 10 days every 28 days during 12 months
  • Active Comparator: Fludarabine
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
366
December 2008
 

Inclusion Criteria:

Established diagnosis of Waldenström macroglobulinemia (the 2nd Workshop on Waldenstrom's macroglobulinemia) or Lymphoplasmacytic lymphoma or Splenic Marginal Zone Lymphoma, needing a treatment

  • Life expectancy > 6 months
  • Creatinine < 200 µmol/l
  • SGPT and SGOT < 2x ULN
  • A negative direct Coombs test
  • Written informed consent

Exclusion Criteria:

  • Past chemotherapy/radiotherapy/immunotherapy prior to the study for Waldenström macroglobulinemia
  • Previous malignancy less than 5 years ago except carcinoma in situ of the cervix and non-melanoma skin cancer
  • Positive HIV serology
  • Active Hepatitis B or C
  • Lactation/pregnancy
  • Impossible good compliance with the study protocol
  • Active infection not controlled
  • Psychological condition hampering understanding of the study
  • Transformation into large B cell lymphoma
  • Peripheral neuropathy > grade II
Both
18 Years and older
No
Contact: Véronique LEBLOND, Professor 33 1 42 16 28 24 veronique.leblond@psl.aphp.fr
France
 
NCT00566332
Pr Véronique LEBLOND, French Study Group on Chronic Lymphoid Leukemia
WM1
French Study Group on Chronic Lymphoid Leukemia
  • Groupe d'Etudes de Lymphomes de L'Adulte
  • Groupe Ouest Est d'Etude des Leucémies et Autres Maladies du Sang GOELAMS
  • Département de Biostatistiques et Informatique Médicale DBIM
Principal Investigator: Véronique LEBLOND, Professor French Study Group on Chronic Lymphoid Leukemia
French Study Group on Chronic Lymphoid Leukemia
November 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP