4.5 Article

Escalating-dose HLA-mismatched DLI is safe for the treatment of leukaemia relapse following alemtuzumab-based myeloablative allo-SCT

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BONE MARROW TRANSPLANTATION
卷 48, 期 10, 页码 1324-1328

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/bmt.2013.69

关键词

GVHD; relapse; DLI

资金

  1. Leuka [286231]
  2. National Institute for Health Research (NIHR) Biomedical Research Centre
  3. National Institute for Health Research [NF-SI-0611-10275, ACF-2008-21-030] Funding Source: researchfish

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Although the feasibility of using HLA-mismatched unrelated donors as an alternate graft source for haematopoietic SCT (HSCT) has been shown, little is known about the safety of HLA-mismatched DLI for the treatment of relapse. We examined the outcome of 58 consecutive leukaemia patients who received escalating-dose DLI for treatment of relapse after alemtuzumab-conditioned myeloablative unrelated donor HSCT at our institution. High-resolution HLA typing on stored DNA samples revealed mismatches in 28/58 patients who were considered HLA-matched at the time of transplantation. Following DLI from HLA-matched (10/10) (n=30) or -mismatched (7-9/10) (n=28) unrelated donors, we found no significant difference in the incidence of acute GVHD (17.2% versus 23.1%, P=0.59), probability of remission at 3 years (62.1% versus 63.9%, P=0.89) or 5-year OS (89.8% versus 77.7%, P=0.22). We conclude that escalating-dose DLI can be safely given to HLA-mismatched recipients following T-depleted myeloablative HSCT.

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