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The effect of allogeneic stem cell transplantation on high risk chronic lymphocytic leukaemia: a single centre retrospective analysis

✍ Scribed by V Válková; J Schwarz; A Vítek; M Marková; D Pohlreich; K Benešová; K Michalová; P Cetkovský; M Trněný


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
279 KB
Volume
29
Category
Article
ISSN
0278-0232

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✦ Synopsis


Abstract

In recent years, many studies have confirmed that allogeneic stem cell transplantation (allo‐SCT) can provide long‐term disease control and possible cure in selected patients with chronic lymphocytic leukaemia (CLL), including those with a biologically highly unfavourable risk profile. A retrospective analysis of allo‐SCT in 30 patients with CLL whose risk profile was unfavourable and who were treated in the years 2000–2009 was performed. The aim was to compare the results of allo‐SCT by prognostic factors and conditioning type and evaluate the results of unrelated transplantation. The median age was 54 years. Donors were 8 HLA‐matched siblings and 22 unrelated volunteers, 11 of whom were mismatched. Eighteen patients were treated with reduced intensity conditioning. Twelve patients received myeloablative conditioning. Estimated overall survival (OS) at 3 years was 78%, progression‐free survival (PFS) 71%, relapse incidence 10% and non‐relapse mortality (NRM) 16%, respectively, with a median follow‐up of 35 months. According to molecular/cytogenetic characteristics, OS and PFS for the high risk group (17p‐ or 11q‐) were 89 and 77%, respectively, not significantly different from those with standard risk. Graft‐versus‐host disease (GVHD) was associated with greater toxicity; significantly higher NRM for patients with aGVHD (p = 0.04) and worse PFS for patients with cGVHD (p = 0.04). Our results for the refractory disease group (77% responses) indicate that chemoresistance may be overcome by the GVL effect. Transplants from unrelated donors may be considered comparable to those from related donors. Copyright © 2010 John Wiley & Sons, Ltd.