The purpose of this study is to determine whether the rituximab administration with fludarabine and cyclophosphamide results, are better, than the ones obtained with conventional therapy such as CHOP (cyclophosphamide, adriamycin, vincristine, prednisone) and also to determine whether the rituximab administration as maintenance treatment during two years, increase the global clinical responses and the disease free time interval.
The use of monoclonal antibodies, specifically the chimerical humanized anti-CD20 monoclonal antibody (Rituximab, MabThera®) represents one of the most innovative aspects in the indolent lymphoma treatment. Preliminary data show from 40% to 50% of response with a median response duration between 6 and 11 months in patients with relapsing FL. This response rate increase when rituximab is administered as initial treatment. Therefore, not only due to the clinical results but also to the tolerance, and based on an innovative mechanism of action and in its minimal toxicity, it seems reasonable to raise the possibility to incorporate the administration of the monoclonal antibody with chemotherapeutic agents. The development of a new treatment scheme that includes Rituximab administration within treatment protocols that combine fludarabine and cyclophosphamide, whose results are better than the ones obtained with conventional treatments such as CHOP, should increase the molecular response rate and contribute therefore to increase the disease-free time interval (time to progression), without adding any toxicity, in addition to achieve a higher proportion of clinical responses (as global as complete responses). In order to increase the time interval to progression, a maintenance treatment will be carried out for 2 years, which has shown an evident benefit in the time to progression in preliminary studies.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
75
Patients receiving from 4 to 6 cycles of chemotherapy (R F C) each 4 weeks depending on haematological tolerance: RITUXIMAB(R)375 mg/m2 iv,day 3 C1 and day 1 C2-C6,(total dose 375 mg/m2) FLUDARABINE(F):25 mg/m2 iv, day 1-3,(total dose 75 mg/m2) CICLOPHOSPHAMIDE(C)1000 mg/m2 iv, day 1,(total dose 1000 mg/m2)
Hospital Infanta Cristina
Badajoz, Badajoz_Extremadura, Spain
Hospital del Mar
Barcelona, Barcelona_ Cataluña, Spain
Instituto Catalán de Oncología (ICO)
Barcelona, Barcelona_Cataluña, Spain
Hospital San Pedro de Alcántara
Cáceres, Cáceres_Extremadura, Spain
Hospital de Puerto Real
Puerto Real, Cádiz_ Andalucía, Spain
Complejo Hospitalario Xeral_Calde
Lugo, Lugo_ Galicia, Spain
Hospital Universitario Príncipe de Asturias
Alcalá de Henares, Madrid, Spain
Fundación Hospital Alcorcón
Alcorcón, Madrid, Spain
Hospital de Fuenlabrada
Fuenlabrada, Madrid, Spain
Hospital Severo Ochoa
Leganés, Madrid, Spain
...and 10 more locations
Time to progression disease
Time frame: 42 months
Free-disease period
Time frame: 54 months
Overall survival
Time frame: 54 months
Safety of RFC
Toxicity is detailed and tabulate following the WHO classification. The safety analysis includes the incidence of adverse events (AE),vital signs and laboratory parameters. Impact tables are made of AE following the classification of preferred term. Also include an analysis of the intensity of AE and their relation to the combiantion of study treatment.
Time frame: 54 months
Molecular monitoring of clinical response
Study of t14:18 translocation with altered expression of BCL2.
Time frame: 54 months
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