ConclusionHaplo-HSCT in 1 and 2 remissions of AL allows to achieve 10-year OS in 64.7% of children, while the type of acute leukemia does not influence the outcome of haplo-HSCT. The acceptable frequency of development of aGVHD III 0 -IV 0 -18.6% allows to treat haplo-HSCT as therapy in 1 and 2 remissions of high risk group. The main complication of haplo-HSCT is relapse -23.5% in the early posttransplant period to D + 100.
О р и г и н а л ь н ы е и с с л е д о в а н и я / О б з о р ы л и т е р а т у р ы Инвазивные микозы у реципиентов аллогенной трансплантации гемопоэтических стволовых клеток подросткового возраста и молодых взрослых
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