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Maintenance therapy with rituximab leads to a significant prolongation of response duration after salvage therapy with a combination of rituximab, fludarabine, cyclophosphamide, and mitoxantrone (R-FCM) in patients with recurring and refractory follicular and mantle cell lymphomas: Results of a prospective randomized study of the German Low Grade Lymphoma Study Group (GLSG).

Authors :
Forstpointner R
Unterhalt M
Dreyling M
Böck HP
Repp R
Wandt H
Pott C
Seymour JF
Metzner B
Hänel A
Lehmann T
Hartmann F
Einsele H
Hiddemann W
Source :
Blood [Blood] 2006 Dec 15; Vol. 108 (13), pp. 4003-8. Date of Electronic Publication: 2006 Aug 31.
Publication Year :
2006

Abstract

In follicular lymphoma (FL) and mantle cell lymphoma (MCL) the monoclonal antibody rituximab (R) improves the prognosis when combined with chemotherapy. The present study investigated R-maintenance after R-chemotherapy. Patients with recurring or refractory FL and MCL were randomized to 4 courses of fludarabine, cyclophosphamide, and mitoxantrone (FCM) alone or combined with R (R-FCM). Responding patients underwent a second randomization for R-maintenance comprising 2 further courses of 4-times-weekly doses of R after 3 and 9 months. The first randomization was stopped after 147 patients, when R-FCM revealed a significantly better outcome. All subsequent patients received R-FCM. Of the 176 patients who are currently evaluable (as of October 2005), 138 received R-FCM for remission induction. Response duration was significantly prolonged by R-maintenance after R-FCM, with the median not being reached in this evaluation versus an estimated median of 16 months (P = .001). This beneficial effect was also observed when analyzing FL (P = .035) and MCL (P = .049) separately. Hence, R-maintenance is effective after salvage with R-chemotherapy and significantly prolongs response duration in patients with recurring or refractory FL or MCL.

Details

Language :
English
ISSN :
0006-4971
Volume :
108
Issue :
13
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
16946304
Full Text :
https://doi.org/10.1182/blood-2006-04-016725