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首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Outcomes of Adults with Acute Lymphoblastic Leukemia Relapsing after Allogeneic Hematopoietic Stem Cell Transplantation
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Outcomes of Adults with Acute Lymphoblastic Leukemia Relapsing after Allogeneic Hematopoietic Stem Cell Transplantation

机译:异基因造血干细胞移植后成人急性淋巴细胞白血病复发的结果

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For patients with acute lymphoblastic leukemia (ALL) who relapse after allogeneic hematopoietic stem cell transplantation (HSCT), treatment options are limited, and the clinical course and prognostic factors affecting outcome have not been well characterized. We retrospectively analyzed outcomes of 123 adult patients with ALL who relapsed after a first HSCT performed at our center between 1993 and 2011. First-line salvage included second HSCT (n= 19), donor lymphocyte infusion with or without prior chemotherapy (n= 11), radiation therapy (n= 6), cytoreductive chemotherapy (n= 30), mild chemotherapy (n= 27), or palliative care (n= 23), with median postrelapse overall survival (OS) of 10 months, 6.5 months, 3 months, 4 months, 4months, and 1 month, respectively. Despite a complete remission rate of 38% after first-line salvage in the treated patients, the OS rate remained limited with 1- and 2- year OS rates of 17% (95% confidence interval, 13 to 29) and 10% (95% confidence interval, 6 to 20), respectively. On univariate analysis, adverse factors for OS included active disease at the time of first HSCT and short time to progression from first HSCT (<6 months). There was no difference in the 6-month survival postrelapse in patients with isolated extramedullary relapse (44%) compared with combined extramedullary and bone marrow relapse (29%) or those with isolated bone marrow relapse (34%) (P= 8). Our data provide more insight into the disease behavior and treatment outcomes of ALL at relapse after HSCT against which future trials may be compared.
机译:对于同种异体造血干细胞移植(HSCT)后复发的急性淋巴细胞白血病(ALL)患者,治疗选择有限,影响结果的临床过程和预后因素尚未得到很好的表征。我们回顾性分析了1993年至2011年在我们中心进行的首次HSCT后复发的123例ALL患者的结局。一线挽救包括第二次HSCT(n = 19),供体淋巴细胞输注或未接受化疗(n = 11) ),放疗(n = 6),细胞减少化疗(n = 30),轻度化疗(n = 27)或姑息治疗(n = 23),其中复发后总体生存时间(OS)为10个月,6.5个月,分别为3个月,4个月,4个月和1个月。尽管接受一线治疗后患者的完全缓解率达到38%,但OS率仍然受到限制,其中1年和2年OS率分别为17%(95%置信区间为13至29)和10%(95) %置信区间(6到20)。在单因素分析中,OS的不利因素包括第一次HSCT时的活动性疾病和从第一次HSCT到进展的短时间(<6个月)。单纯髓外复发(44%)与单纯髓外和骨髓合并复发(29%)或单纯骨髓复发(34%)患者的6个月生存期无差异(P = 8)。我们的数据提供了更多关于HSCT复发后ALL的疾病行为和治疗结果的见解,可以与将来的试验进行比较。

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