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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00503594
Other study ID # P060239
Secondary ID
Status Recruiting
Phase Phase 2
First received July 18, 2007
Last updated July 27, 2012
Start date July 2007
Est. completion date July 2012

Study information

Verified date July 2007
Source Assistance Publique - Hôpitaux de Paris
Contact Antonio OMURO, MD,PhD
Phone + 33(0) 1 42 16 41 60
Email antonio.omuro@psl.aphp.fr
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

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


Description:

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 92
Est. completion date July 2012
Est. primary completion date July 2010
Accepts healthy volunteers No
Gender Both
Age group 60 Years and older
Eligibility 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

Study Design

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


Related Conditions & MeSH terms


Intervention

Drug:
Methotrexate and temozolomide
Methotrexate and temozolomide
Methotrexate , procarbazine ,vincristine ,cytarabine
Methotrexate , procarbazine ,vincristine ,cytarabine

Locations

Country Name City State
France Groupe hospitalier la Pitié Salpétrière Paris

Sponsors (2)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris Groupe Ouest Est d'Etude des Leucémies et Autres Maladies du Sang GOELAMS

Country where clinical trial is conducted

France, 

References & Publications (1)

Omuro AM, Abrey LE. Chemotherapy for primary central nervous system lymphoma. Neurosurg Focus. 2006 Nov 15;21(5):E12. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Progression-free survival at one year Yes
Secondary Overall survival:median and overall survival at one and two years Yes
Secondary Response rates at end of treatment Yes
Secondary Toxicity during treatment Yes
Secondary Late toxicity 2 to 5 years after treatment Yes
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