Lymphoma, Follicular, Lymphoma, Low-Grade, Lymphoma, Intermediate-Grade
Conditions
Keywords
Drug Therapy, Maintenance, rituximab
Brief summary
The aim of this phase III trial is to assess the safety and efficacy of treatment with rituximab in combination with FCM chemotherapy (R-FCM) versus FCM chemotherapy alone for remission induction and to asses the safety and efficacy of rituximab maintenance versus observation only after response to induction therapy. Both questions are addressed in way of a prospective randomized comparison in patients with relapsed FL, MCL and LP lymphoma.
Detailed description
Patients with relapsed centroblastic/centrocytic (FL), centrocytic (MCL)or lymphoplasmacytoid lymphoma are randomly assigned to either FCM chemotherapy alone or to FCM chemotherapy in combination with the monoclonal anti-CD20 antibody rituximab (R-FCM). FCM chemotherapy will be given for 4 cycles in intervals of 4 weeks. In patients assigned to cytoreductive therapy with FCM plus rituximab, the monoclonal antibody is given as one infusion (375 mg/m2) on the day before the respective FCM course for a total of four applications. Four weeks after the end of FCM chemotherapy patients with CR or PR are randomly assigned to either no further treatment or maintenance therapy with rituximab. Rituximab will be given 4 times (one infusion per week with 375 mg/m2). After six months rituximab treatment will be repeated with another 4 infusions. In case of relapse patients will receive an alternative treatment according to the decision of the investigator. The aim of this phase III trial is to assess the safety and efficacy of treatment with rituximab in combination with FCM chemotherapy versus FCM chemotherapy alone for remission induction and to asses the safety and efficacy of rituximab maintenance versus observation only after response to induction therapy. Both questions are addressed in way of a prospective randomized comparison in patients with relapsed FCL, MCL and LP lymphoma. Primary objectives of this trial are to compare (1) the remission rates (CR and PR) achieved after FCM plus rituximab versus FCM alone and (2) the progression free interval of rituximab maintenance versus observation only.
Interventions
PROCEDUREFCM
Active comparator: Chemotherapy
PROCEDURER-FCM
experimental: Chemotherapy with additional rituximab
2 courses of rituximab maintenance after completion of salvage therapy
OTHERobservation only
no Intervention after completion of FCM or R-FCM
Sponsors
Ludwig-Maximilians - University of Munich
Study design
Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* patients with histologically proven stage III/IV centroblastic/centrocytic (FL), centrocytic (MCL)or lymphoplasmacytoid lymphoma (LPIC). * relapsed disease after initial chemotherapy or peripheral blood stem cell transplantation * two-dimensionally measurable lesion outside a previously irradiated area (osteoblastic bone lesions, ascites, and pleural effusions are not evaluable) * age \> 18 years * Karnofsky-index \> 60 * life expectancy of at least 3 months * effective contraception in female premenopausal patients * patient's written informed consent
Exclusion criteria
* age \< 18 years * Karnofsky-index \< 60 * treatment with fludarabine or mitoxantrone within the preceding three months * active auto-immune hemolytic anemia at the start of FCM chemotherapy * participation in another clinical trial during the last 4 weeks * participation in this study before * previous treatment with murine antibodies * concurrent diseases which exclude the administration of therapy as outlined by the study protocol * non-compensated heart failure * dilatative cardiomyopathy * coronary heart disease with ST segment depression in ECG * myocardial infarction during the last 6 months * chronic lung disease with hypoxemia * severe non-compensated hypertension * severe non-compensated diabetes mellitus * renal insufficiency (creatinine \> 2.0 mg/dl), not related to lymphoma * hepatic insufficiency with transaminase values greater than 3-fold of normal values and/or bilirubin levels \> 2.0 mg/dl, not related to lymphoma * clinical signs of cerebral dysfunction * women during lactation or pregnancy or of childbearing potential not using a reliable contraceptive method * severe psychiatric disease * serological positivity for HBV, HCV, HIV * previous organ transplantation other than autologous peripheral blood stem cell transplantation * missing written informed consent or missing written consent for data protection
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Remission rate | — |
| Event free interval | — |
Secondary
| Measure | Time frame |
|---|---|
| Time to Progression | — |
| Overall survival | — |
| adverse events | — |
| serious infectious complications | — |
Countries
Germany
Outcome results
None listed