Salvage therapy for acute chemorefractory leukemia by allogeneic stem cell transplantation: the Korean experience
Little is known about the characteristics that make patients with acute leukemia suitable for undergoing salvage therapy by allogeneic hematopoietic stem cell transplantation (allo-HSCT). Here, we analyzed the clinical outcomes of 223 patients with acute leukemia who underwent allo-HSCT while not in...
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Veröffentlicht in: | Annals of hematology 2017-04, Vol.96 (4), p.605-615 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Little is known about the characteristics that make patients with acute leukemia suitable for undergoing salvage therapy by allogeneic hematopoietic stem cell transplantation (allo-HSCT). Here, we analyzed the clinical outcomes of 223 patients with acute leukemia who underwent allo-HSCT while not in complete remission (CR). The primary end points were overall survival (OS) and CR rate. CR was achieved in 79.8% of patients after allo-HSCT. Acute graft-versus-host disease (GVHD) was significantly associated with CR (
P
= 0.045). During a median follow-up of 30.1 months, the median OS was 6.1 months. OS was significantly longer in patients with good or standard risk cytogenetic characteristics than in those with poor risk cytogenetic characteristics (
P
= 0.029,
P
= 0.030, respectively). Patients who received allo-HSCT from a matched sibling donor had better survival than those with unrelated donors (
P
= 0.015). Primary chemorefractoriness was not associated with poor survival (
P
= 0.071). The number of chemotherapies before allo-HSCT was significantly correlated with outcome (
P
= 0.006). Chronic GVHD was a strong predictor of a longer OS (
P
= 0.025). In conclusion, survival of patients with primary chemorefractory acute leukemia is not lower when treated upfront with allo-HSCT. Hence, allo-HSCT should be actively considered in such patients. Acute and chronic GVHD is associated with better outcomes patients with acute leukemia who have undergone allo-HSCT and not achieved CR. |
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ISSN: | 0939-5555 1432-0584 |
DOI: | 10.1007/s00277-017-2919-8 |