Nasal/nasal type NK-T-cell lymphoma is a rare and severe type of non-Hodgkin's lymphoma (NHL) more frequent in Asia than in western countries. When localised, radiotherapy seems to be the best treatment. When radiotherapy cannot be used because of dissemination or relapse, chemotherapy protocols used for other types of NHL give poor results and survival is poor. Recently papers from China and Japan reported the efficacy of a drug: l-asparaginase, usually used to treat acute lymphoblastic leukemia. In vitro a selective apoptosis of NK-cell tumours by l-asparaginase was shown on tumour cell lines and samples. The investigators propose a phase II protocol for patients with refractory or relapsing nasal/nasal type NK-T-cell lymphoma using a regimen combining l-asparaginase, methotrexate and dexamethasone. Biological studies will be conducted trying to find factors which could predict responses to this chemotherapy. Since january 2009, the study concerns all patients with nasal/nasal type NK-T-cell lymphoma who have not received asparaginase before.
Primary Objective: * Determine the overall and complete response rate Secondary Objectives: * To evaluate survival without progression * To evaluate total survival. * To evaluate the tolerance and the side effects of the treatment. * To evaluate the duration and the mode of hospitalization of the patients treated by this therapeutic association. * To constitute a bank of biological samples - serum, tumoral, ADN, ARN to allow prognostic studies implying virus EBV, p53, CD94, C-kit and asparagine synthetase gene in order to better understand the mechanisms of the cancerogenesis of this variety of cytotoxic LNH and to identify the predictive factors of response to the asparaginase. Sampling: For each patient included in the protocol, the following sampling will be carried out with the diagnosis: * Biopsy, * Medullary biopsy * Medullary aspiration * blood: 3 tubes of 7 ml on EDTA and 3 tubs of 7 ml with heparin Treatment: All the patients included will receive three cures separated by 3 weeks (J1, J22, J43): * J1: Methotrexate 3 gr/m2 * J2, J4, J6 and J8: Kidrolase® 6000 u/m2 * J1 with J4: Dexamethasone 40 mg (20 mg if age \> 70 years)
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
40
6000 u/ m2 IM at J2, J4 and J6 and J8. 3 to 6 cycles.
3 gr/m2 at J1
40 mg/ per os at J1, J2 and J4.
In case of allergy to Kidrolase 20000 u/m2 en IM at J2, J4, J6 et J8. 3 to 6 cycles
Département Maladies du Sang
Angers, France
CH Annecy
Annecy, France
Service de Radiothérapie, Polyclinique Bordeaux Nord
Bordeaux, France
CHU Bordeaux
Bordeaux, France
Service d'Hématologie Clinique - Hôpital Henri Mondor
Créteil, France
Service d'Hématologie Clinique, CHU Dijon
Dijon, France
Service d'Hématologie
Évry, France
CHU Grenoble-Hématologie Clinique
Grenoble, France
CHU Lille - Maladies du Sang
Lille, France
Service d'Hématologie et de Thérapie Cellulaire - CHU Limoges
Limoges, France
...and 15 more locations
Efficacy of chemotherapy
Time frame: 3 month, 6 month, 9 month, 12 month, 18 month, 24 month
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