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Original Articles: Clinical

Retreatment with rituximab in 178 patients with relapsed and refractory B-cell lymphomas: a single institution case control study

, , , , , & show all
Pages 399-405 | Received 23 Aug 2009, Accepted 21 Nov 2009, Published online: 28 Dec 2009
 

Abstract

The role of rituximab retreatment in relapsed B-cell lymphoma is not well known. We undertook a single center retrospective cohort study to investigate the efficacy of retreatment with rituximab with or without chemotherapy in patients with relapsed and refractory B-cell lymphomas. We only included patients treated first-line and in first progression; 178 patients were included in the study, of whom 29% had diffuse large B-cell lymphoma (DLBCL) and 28% had follicular lymphoma (FL). The overall response rate for the first treatment was 81% and for the second treatment was 66%. The median progression-free survival (PFS) for all patients from diagnosis was 13.2 months and from relapse was 12.5 months (not statistically different). For DLBCL the median PFS from diagnosis was 9.6 months and from relapse was 8.4 months, and for FL the median PFS from diagnosis was 26.4 months and from relapse was 19.2 months (not statistically different). The 5-year overall survival was 57%. In a historical comparison with rituximab-naive patients, rituximab-retreated patients had a shorter time to initial relapse than control patients, but there was no difference between the two groups for PFS from relapse. In conclusion, retreatment with rituximab, with or without chemotherapy, yields a high overall response rate in patients with relapsed and refractory B-cell lymphomas. Relapse occurring after rituximab-containing therapy appears to be more aggressive than that occurring after chemotherapy alone. The outcome of retreatment, in terms of progression-free survival, is similar to that of primary treatment.

Acknowledgements

We gratefully acknowledge the assistance of the staff of the Department of Clinical Hematology at Centre Hospitalier Lyon-Sud.

Declaration of interest: Roche, France, supplied a small grant to enable this study to proceed, but had no role in the collection or analysis of the data or preparation of the manuscript. One of the authors (A.J.) was supported by scholarships from the Goddard-Sapin Jaloustre Scholarship Trust, Bourse Michel Clavel, Royal College of Pathologists of Australasia, and the Royal North Shore Hospital, Sydney, Australia.

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