Rituximab purging and maintenance combined with auto-SCT: long-term molecular remissions and prolonged hypogammaglobulinemia in relapsed follicular …

LK Hicks, A Woods, R Buckstein, J Mangel… - Bone marrow …, 2009 - nature.com
LK Hicks, A Woods, R Buckstein, J Mangel, N Pennell, L Zhang, K Imrie, D Spaner…
Bone marrow transplantation, 2009nature.com
We enrolled 23 patients with relapsed follicular lymphoma (FL) in a prospective single-arm
study of auto-SCT combined with in vivo rituximab graft purging and post transplant
rituximab maintenance. Minimal residual disease was monitored with quantitative PCR
testing. With a median follow-up of 74.2 months, neither median overall survival (OS) nor
PFS has been reached. Here, 5-year OS and 5-year PFS are 78%(95% confidence interval
(CI) 61–95%) and 59%(95% CI 38–80%), respectively. Time to progression (TTP) with the …
Abstract
We enrolled 23 patients with relapsed follicular lymphoma (FL) in a prospective single-arm study of auto-SCT combined with in vivo rituximab graft purging and post transplant rituximab maintenance. Minimal residual disease was monitored with quantitative PCR testing. With a median follow-up of 74.2 months, neither median overall survival (OS) nor PFS has been reached. Here, 5-year OS and 5-year PFS are 78%(95% confidence interval (CI) 61–95%) and 59%(95% CI 38–80%), respectively. Time to progression (TTP) with the experimental regimen was significantly improved compared with TTP with the last prior treatment (P< 0.001). Durable molecular remissions occurred in 11 of 13 assessable patients. PFS was significantly longer in patients who achieved a molecular remission by 3 months post-auto-SCT (P= 0.001). Prolonged hypogammaglobulinemia occurred in most patients; however, no increase in major infections was observed.
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