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Trial Comparing Chlorambucil to Fludarabine in Patients With Advanced Waldenström Macroglobulinemia

Primary Purpose

Waldenström Macroglobulinemia, Lymphoplasmacytic Lymphoma, Splenic Marginal Zone Lymphoma

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Chlorambucil
Fludarabine
Sponsored by
French Study Group on Chronic Lymphoid Leukemia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Waldenström Macroglobulinemia focused on measuring Waldenström Macroglobulinemia, Lymphoplasmacytic lymphoma, Splenic Marginal Zone Lymphoma, Fludarabine, Chlorambucil

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Hôpital La Pitié-Salpêtrière. 47-83 Bd de l'hôpital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

Chlorambucil 8mg/m² (6 mg/m² if patient aged more than 75 years old) 10 days every 28 days during 12 months

Fludarabine

Outcomes

Primary Outcome Measures

Patient overall response

Secondary Outcome Measures

Biological study
Quality of life
Response duration
Treatment toxicity
Event free survival
Overall survival

Full Information

First Posted
November 30, 2007
Last Updated
August 18, 2015
Sponsor
French Study Group on Chronic Lymphoid Leukemia
Collaborators
Lymphoma Study Association, French Innovative Leukemia Organisation, Département de Biostatistiques et Informatique Médicale DBIM
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1. Study Identification

Unique Protocol Identification Number
NCT00566332
Brief Title
Trial Comparing Chlorambucil to Fludarabine in Patients With Advanced Waldenström Macroglobulinemia
Official Title
Randomized Trial Comparing the Efficacy of Chlorambucil to Fludarabine in Patients With Advanced Waldenström Macroglobulinemia,Lymphoplasmacytic Lymphoma or Splenic Marginal Zone Lymphoma
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
June 2001 (undefined)
Primary Completion Date
September 2009 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
French Study Group on Chronic Lymphoid Leukemia
Collaborators
Lymphoma Study Association, French Innovative Leukemia Organisation, Département de Biostatistiques et Informatique Médicale DBIM

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Waldenström Macroglobulinemia, Lymphoplasmacytic Lymphoma, Splenic Marginal Zone Lymphoma
Keywords
Waldenström Macroglobulinemia, Lymphoplasmacytic lymphoma, Splenic Marginal Zone Lymphoma, Fludarabine, Chlorambucil

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
414 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Chlorambucil 8mg/m² (6 mg/m² if patient aged more than 75 years old) 10 days every 28 days during 12 months
Arm Title
2
Arm Type
Active Comparator
Arm Description
Fludarabine
Intervention Type
Drug
Intervention Name(s)
Chlorambucil
Intervention Description
Chlorambucil 8 mg/m² (6 mg/m² if patient aged more than 75 years old) 10 days every 28 days during 12 months By oral route
Intervention Type
Drug
Intervention Name(s)
Fludarabine
Intervention Description
Fludarabine 40 mg/m² (30 mg/m² if patient aged more than 75 years old) 5 days every 28 days during 6 cycles By oral route
Primary Outcome Measure Information:
Title
Patient overall response
Time Frame
At the end of treatment whether 6 or 12 months
Secondary Outcome Measure Information:
Title
Biological study
Time Frame
Whether 6 or 12 months
Title
Quality of life
Time Frame
Whether 6 or 12 months
Title
Response duration
Time Frame
60 months
Title
Treatment toxicity
Time Frame
60 months
Title
Event free survival
Time Frame
60 months
Title
Overall survival
Time Frame
60 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Véronique LEBLOND, Professor
Organizational Affiliation
French Study Group on Chronic Lymphoid Leukemia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital La Pitié-Salpêtrière. 47-83 Bd de l'hôpital
City
Paris
ZIP/Postal Code
75013
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
23233721
Citation
Leblond V, Johnson S, Chevret S, Copplestone A, Rule S, Tournilhac O, Seymour JF, Patmore RD, Wright D, Morel P, Dilhuydy MS, Willoughby S, Dartigeas C, Malphettes M, Royer B, Ewings M, Pratt G, Lejeune J, Nguyen-Khac F, Choquet S, Owen RG. Results of a randomized trial of chlorambucil versus fludarabine for patients with untreated Waldenstrom macroglobulinemia, marginal zone lymphoma, or lymphoplasmacytic lymphoma. J Clin Oncol. 2013 Jan 20;31(3):301-7. doi: 10.1200/JCO.2012.44.7920. Epub 2012 Dec 10.
Results Reference
derived
PubMed Identifier
23065509
Citation
Nguyen-Khac F, Lambert J, Chapiro E, Grelier A, Mould S, Barin C, Daudignon A, Gachard N, Struski S, Henry C, Penther D, Mossafa H, Andrieux J, Eclache V, Bilhou-Nabera C, Luquet I, Terre C, Baranger L, Mugneret F, Chiesa J, Mozziconacci MJ, Callet-Bauchu E, Veronese L, Blons H, Owen R, Lejeune J, Chevret S, Merle-Beral H, Leblondon V; Groupe Francais d'Etude de la Leucemie Lymphoide Chronique et Maladie de Waldenstrom (GFCLL/MW); Groupe Ouest-Est d'etude des Leucemie Aigues et Autres Maladies du Sang (GOELAMS); Groupe d'Etude des Lymphomes de l'Adulte (GELA). Chromosomal aberrations and their prognostic value in a series of 174 untreated patients with Waldenstrom's macroglobulinemia. Haematologica. 2013 Apr;98(4):649-54. doi: 10.3324/haematol.2012.070458. Epub 2012 Oct 12.
Results Reference
derived

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Trial Comparing Chlorambucil to Fludarabine in Patients With Advanced Waldenström Macroglobulinemia

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