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- Title
Treatment of refractory chronic GVHD with rituximab: a GITMO study.
- Authors
Zaja, F.; Bacigalupo, A.; Patriarca, F.; Stanzani, M.; Van Lint, M. T.; Filì, C.; Scimè, R.; Milone, G.; Falda, M.; Vener, C.; Laszlo, D.; Alessandrino, P. E.; Narni, F.; Sica, S.; Olivieri, A.; Sperotto, A.; Bosi, A.; Bonifazi, F.; Fanin, R.
- Abstract
The anti-CD20 chimaeric monoclonal antibody Rituximab has recently been shown to induce significant clinical response in a proportion of patients with refractory chronic graft-versus-host disease (cGVHD). We now report 38 patients, median age 48 years (22–61), receiving Rituximab for refractory cGVHD, assessed for clinical response and survival. Median duration of cGVHD before Rituximab was 23 months (range 2–116), the median number of failed treatment lines was 3 (range 1 to 6) and the median follow-up after Rituximab was 11 months (1–88). Overall response rate was 65%: skin 17/20 (63%), mouth 10/21 (48%), eyes 6/14 (43%), liver 3/12 (25%), lung 3/8 (37.5%), joints 4/5, gut 3/4, thrombocytopaenia 2/3, vagina 0/2, pure red cell aplasia 0/1 and, myasthenia gravis 1/1. During the study period 8/38 died: causes of death were cGVHD progression (n=3), disease relapse (n=1), infection (n=3), sudden death (n=1). The actuarial 2 year survival is currently 76%. We confirm that Rituximab is effective in over 50% of patients with refractory cGVHD and may have a beneficial impact on survival.Bone Marrow Transplantation (2007) 40, 273–277; doi:10.1038/sj.bmt.1705725; published online 4 June 2007
- Subjects
GRAFT versus host disease; RITUXIMAB; BONE marrow transplant complications; MONOCLONAL antibodies; PURE red cell aplasia; MYASTHENIA gravis; THERAPEUTICS
- Publication
Bone Marrow Transplantation, 2007, Vol 40, Issue 3, p273
- ISSN
0268-3369
- Publication type
Article
- DOI
10.1038/sj.bmt.1705725