Methotrexate and Temozolomide Versus Methotrexate, Procarbazine, Vincristine and Cytarabine (CNSLymphoma)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2007 by Assistance Publique - Hôpitaux de Paris.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
Groupe Ouest Est d'Etude des Leucémies et Autres Maladies du Sang GOELAMS
Information provided by (Responsible Party):
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT00503594
First received: July 18, 2007
Last updated: July 27, 2012
Last verified: July 2007

July 18, 2007
July 27, 2012
July 2007
July 2010   (final data collection date for primary outcome measure)
Progression-free survival [ Time Frame: at one year ] [ Designated as safety issue: Yes ]
Progression-free survival [ Time Frame: at one year ]
Complete list of historical versions of study NCT00503594 on ClinicalTrials.gov Archive Site
  • Overall survival:median and overall survival [ Time Frame: at one and two years ] [ Designated as safety issue: Yes ]
  • Response rates [ Time Frame: at end of treatment ] [ Designated as safety issue: Yes ]
  • Toxicity [ Time Frame: during treatment ] [ Designated as safety issue: Yes ]
  • Late toxicity [ Time Frame: 2 to 5 years after treatment ] [ Designated as safety issue: Yes ]
  • Overall survival:median and overall survival [ Time Frame: at one and two years ]
  • Response rates [ Time Frame: at end of treatment ]
  • Toxicity [ Time Frame: during treatment ]
  • Late toxicity [ Time Frame: 2 to 5 years after treatment ]
Not Provided
Not Provided
 
Methotrexate and Temozolomide Versus Methotrexate, Procarbazine, Vincristine and Cytarabine
Multicenter Randomized Phase II Study of Methotrexate (MTX) and Temozolomide Versus MTX, Procarbazine, Vincristine and Cytarabine for Primary CNS Lymphoma (PCNSL) in the Elderly

The purpose of this study is to evaluate two types of chemotherapy for primary central nervous system lymphoma in the elderly (age older than 60) :

  • Methotrexate, procarbazine, vincristine and cytarabine
  • Methotrexate and temozolomide

The aim of the study is to evaluate efficacy and toxicity associated with both protocols in this population, without radiotherapy.

Patients will be randomized to receive one of the two regimens in one of the participating centers. Neuropsychological evaluation will be performed in all patients. Patients will be followed with serial MRIs.

Interventional
Phase 2
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Lymphoma
  • Drug: Methotrexate and temozolomide
    Methotrexate and temozolomide
    Other Name: Methotrexate and temozolomide
  • Drug: Methotrexate , procarbazine ,vincristine ,cytarabine
    Methotrexate , procarbazine ,vincristine ,cytarabine
    Other Name: Methotrexate , procarbazine ,vincristine ,cytarabine
  • Experimental: 1
    Comparative evaluation of the efficiency of a new protocol of the primitive LYMPHOME of the central nervous system ( LPSNC) to the old subject, associating Methotrexate and Temozolomide with regard to a standard protocol associating Methotrexate, Procarbazine, Vincristine and Cytarabine.
    Intervention: Drug: Methotrexate and temozolomide
  • Active Comparator: bras conventional
    bras conventional
    Intervention: Drug: Methotrexate , procarbazine ,vincristine ,cytarabine
Omuro AM, Abrey LE. Chemotherapy for primary central nervous system lymphoma. Neurosurg Focus. 2006 Nov 15;21(5):E12. Review.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
92
July 2012
July 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • primary central nervous system lymphoma histologically confirmed by brain biopsy, CSF cytology or vitrectomy
  • KPS 40 or higher
  • Absence of systemic disease as evaluated by chest-abdomen-pelvis CT scan
  • Leucocytes>3.500/mm3, platelets>130.000/mm3, Bilirubin < 2 mg, transaminases < 2.5 N), creatinine < 150 μM/l, creatinine clearance > 40 ml/min
  • Age ≥ 60 years
  • Negative HIV test
  • Signature of informed consent

Exclusion Criteria:

  • previous cranial radiotherapy
  • prior chemotherapy for primary central nervous system lymphoma
  • presence of another cancer (excepting basal cell carcinoma of the skin and cervical carcinoma in situ )
  • systemic lymphoma (outside the CNS)
  • Isolated ocular lymphoma
  • Immunosuppressed patients (HIV , use of immunosuppressors)
  • Other uncontrolled or progressive disease compromising shot-term survival
  • Severe renal or hepatic disease
  • Patients not legally covered by the French Social Security
  • Inability to swallow the medication
Both
60 Years and older
No
Contact: Antonio OMURO, MD,PhD + 33(0) 1 42 16 41 60 antonio.omuro@psl.aphp.fr
France
 
NCT00503594
P060239
Yes
Assistance Publique - Hôpitaux de Paris
Assistance Publique - Hôpitaux de Paris
Groupe Ouest Est d'Etude des Leucémies et Autres Maladies du Sang GOELAMS
Principal Investigator: Antonio OMURO, MD, Assistance Publique - Hôpitaux de Paris
Assistance Publique - Hôpitaux de Paris
July 2007

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