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Safety and Efficacy of an Adult Acute Lymphoblastic Leukemia Chemotherapy for Adult Lymphoblastic Lymphoma

Primary Purpose

Lymphoblastic Lymphoma

Status
Unknown status
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Prednisone, vincristine, daunorubicin , cyclophosphamide , L.-asparaginase, cytosine-arabinoside, methotrexate, etoposide
hematopoietic stem cell allograft
Sponsored by
Centre Henri Becquerel
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lymphoblastic Lymphoma focused on measuring Non-Hodgkin, Lymphoma, Lymphoblastic

Eligibility Criteria

18 Years - 59 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patient with lymphoblastic lymphoma. Aged from 18 to 59 years. Medullary blasts rate less than 20% Non previously treated With or without central nervous system or meningeal involvement. No contra-indication to anthracyclines. No contra-indication to intensive treatments Negative HIV serology test Negative pregnancy test for all female patients of childbearing potential. Able to be regularly followed up. Exclusion Criteria: Evolutive cancer with the exception of non melanoma skin tumours or stage 0 (in situ) cervical carcinoma. Prior treatment with chemotherapy. Lymphoblastic Transformation of chronic myeloid leukaemia Patient unable to be regularly followed-up.

Sites / Locations

  • Chr de La Citadelle
  • Cliniques Universitaires U C L de Mont Godinne
  • C H U D'Angers
  • Centre Hospitalier de La Region Annecienne
  • Chu de Grenoble
  • Centre Hospitalier de Lens
  • Edouard Herriot Hospital
  • Pierre Benite Hospital
  • Institut Paoli Calmettes
  • Saint-Louis Hospital
  • La Pitie Salpetriere Hospital
  • Cochin Hospital
  • Marechal Joffre Hospital
  • Centre Hospitalier de Poitiers
  • Chu de Reims Robert Debre Hospital
  • Centre Henri Becquerel
  • Institut de Cancerologie de La Loire
  • Bretonneau Hospital
  • Chu de Brabois

Outcomes

Primary Outcome Measures

Event free survival

Secondary Outcome Measures

Disease Free Survival ; Complete response rate ; Overall Survival ; Progression rate; Relapse rate ; Central Nervous System or meningeal relapse rate ; medullary relapse rate ; toxicities.

Full Information

First Posted
September 12, 2005
Last Updated
November 6, 2013
Sponsor
Centre Henri Becquerel
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1. Study Identification

Unique Protocol Identification Number
NCT00195871
Brief Title
Safety and Efficacy of an Adult Acute Lymphoblastic Leukemia Chemotherapy for Adult Lymphoblastic Lymphoma
Official Title
A Multicenter, Phase 2 Study, to Evaluate Safety and Efficacy of an Acute Lymphoblastic Leukemia (ALL) Intensive Chemotherapy for Adult Lymphoblastic Lymphoma (LL).
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Unknown status
Study Start Date
February 2004 (undefined)
Primary Completion Date
June 2014 (Anticipated)
Study Completion Date
December 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centre Henri Becquerel

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary objective of this study is to evaluate the safety and the efficacy of an adult "acute lymphoblastic leukaemia" type chemotherapy in patients less than 60 years with lymphoblastic lymphoma. Treatment principle is based on an intensive induction and a delayed intensification.
Detailed Description
Lymphoblastic lymphomas (LL) are rare and represent less than 2% of the malignant non-Hodgkin lymphomas (NHL). The distinction between a LL and an acute lymphoblastic leukaemia (ALL) is difficult; it is arbitrarily based on the percentage of medullary blasts. Above 20% of blasts, it is an ALL. In both cases, the same type of cells is affected: the lymphoblast. Thus the LL were treated either as aggressive NHL or as ALL. The results of the various clinical studies, have shown a best efficacy of ALL type treatments(in terms of overall survival and disease free survival). These treatments are based on an induction phase with reinforced cyclophosphamide and L-asparaginase, and a re-use of the first drugs after consolidation (delayed intensification). The prognostic factors of ALL are now better defined, determining risk groups. According to these prognostic indicators, the allograft could be proposed in first complete remission. Indicators are biological (hyperleukocytosis, chromosomal abnormalities as t(4;11), t(9;22), t(1;19) translocations), clinical (central nervous system involvement), evolutive (salvage therapy needed to obtain complete remission), consideration of early response (cortico-sensibility and chemo-sensibility) and molecular responses (residual disease). On the other hand, the prognostic factors of LL are not well known. This study should permit to better define them. So the prognostic indicators of ALL, in this study, will be decisional for the indication of allograft. This treatment is based on a parallel currently recruiting adult patients with ALL (protocol GRAALL 2003).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphoblastic Lymphoma
Keywords
Non-Hodgkin, Lymphoma, Lymphoblastic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
155 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Prednisone, vincristine, daunorubicin , cyclophosphamide , L.-asparaginase, cytosine-arabinoside, methotrexate, etoposide
Other Intervention Name(s)
nono
Intervention Description
coventional dosages
Intervention Type
Procedure
Intervention Name(s)
hematopoietic stem cell allograft
Intervention Description
conventional procedures
Primary Outcome Measure Information:
Title
Event free survival
Time Frame
2 y
Secondary Outcome Measure Information:
Title
Disease Free Survival ; Complete response rate ; Overall Survival ; Progression rate; Relapse rate ; Central Nervous System or meningeal relapse rate ; medullary relapse rate ; toxicities.
Time Frame
2 y

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
59 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient with lymphoblastic lymphoma. Aged from 18 to 59 years. Medullary blasts rate less than 20% Non previously treated With or without central nervous system or meningeal involvement. No contra-indication to anthracyclines. No contra-indication to intensive treatments Negative HIV serology test Negative pregnancy test for all female patients of childbearing potential. Able to be regularly followed up. Exclusion Criteria: Evolutive cancer with the exception of non melanoma skin tumours or stage 0 (in situ) cervical carcinoma. Prior treatment with chemotherapy. Lymphoblastic Transformation of chronic myeloid leukaemia Patient unable to be regularly followed-up.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephane Lepretre, MD
Organizational Affiliation
Centre Henri Becquerel, Rouen, France
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Hervé Dombret, MD
Organizational Affiliation
Saint-Louis Hospital, Paris, France
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Norbert Ifrah, MD
Organizational Affiliation
Centre Hospitalier Universitaire d'Angers, FRANCE
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chr de La Citadelle
City
Liege
ZIP/Postal Code
4000
Country
Belgium
Facility Name
Cliniques Universitaires U C L de Mont Godinne
City
Yvoir
ZIP/Postal Code
5530
Country
Belgium
Facility Name
C H U D'Angers
City
Angers
ZIP/Postal Code
49033
Country
France
Facility Name
Centre Hospitalier de La Region Annecienne
City
Annecy
ZIP/Postal Code
74011
Country
France
Facility Name
Chu de Grenoble
City
Grenoble
ZIP/Postal Code
38043
Country
France
Facility Name
Centre Hospitalier de Lens
City
Lens
ZIP/Postal Code
62300
Country
France
Facility Name
Edouard Herriot Hospital
City
Lyon
ZIP/Postal Code
69437
Country
France
Facility Name
Pierre Benite Hospital
City
Lyon
ZIP/Postal Code
69495
Country
France
Facility Name
Institut Paoli Calmettes
City
Marseilles
ZIP/Postal Code
13273
Country
France
Facility Name
Saint-Louis Hospital
City
Paris
ZIP/Postal Code
75000
Country
France
Facility Name
La Pitie Salpetriere Hospital
City
Paris
ZIP/Postal Code
75013
Country
France
Facility Name
Cochin Hospital
City
Paris
ZIP/Postal Code
75014
Country
France
Facility Name
Marechal Joffre Hospital
City
Perpignan
ZIP/Postal Code
66046
Country
France
Facility Name
Centre Hospitalier de Poitiers
City
Poitiers
ZIP/Postal Code
86000
Country
France
Facility Name
Chu de Reims Robert Debre Hospital
City
Reims
ZIP/Postal Code
51092
Country
France
Facility Name
Centre Henri Becquerel
City
Rouen
ZIP/Postal Code
76038
Country
France
Facility Name
Institut de Cancerologie de La Loire
City
Saint Priest En Jarez
ZIP/Postal Code
42271
Country
France
Facility Name
Bretonneau Hospital
City
Tours
ZIP/Postal Code
37044
Country
France
Facility Name
Chu de Brabois
City
Vandoeuvre Les Nancy
ZIP/Postal Code
54511
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
14576732
Citation
Le Gouill S, Lepretre S, Briere J, Morel P, Bouabdallah R, Raffoux E, Sebban C, Lepage E, Brice P. Adult lymphoblastic lymphoma: a retrospective analysis of 92 patients under 61 years included in the LNH87/93 trials. Leukemia. 2003 Nov;17(11):2220-4. doi: 10.1038/sj.leu.2403095.
Results Reference
background
Links:
URL
http://www.gela.org
Description
Official site of the Groupe d'Etudes des Lymphomes de l'Adulte (In French)

Learn more about this trial

Safety and Efficacy of an Adult Acute Lymphoblastic Leukemia Chemotherapy for Adult Lymphoblastic Lymphoma

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