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异基因造血干细胞移植后复发的成人急性淋巴细胞白血病的结局。

Outcomes of adults with acute lymphoblastic leukemia relapsing after allogeneic hematopoietic stem cell transplantation.

机构信息

Department of Stem Cell Transplantation and Cellular Therapy, University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.

出版信息

Biol Blood Marrow Transplant. 2013 Jul;19(7):1059-64. doi: 10.1016/j.bbmt.2013.04.014. Epub 2013 Apr 30.

DOI:10.1016/j.bbmt.2013.04.014
PMID:23644077
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8439154/
Abstract

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, 4 months, 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.

摘要

对于在异基因造血干细胞移植 (HSCT) 后复发的急性淋巴细胞白血病 (ALL) 患者,治疗选择有限,并且尚未很好地描述影响结果的临床过程和预后因素。我们回顾性分析了 1993 年至 2011 年期间在我们中心进行的首次 HSCT 后复发的 123 例成人 ALL 患者的结局。一线挽救治疗包括第二次 HSCT(n = 19)、供者淋巴细胞输注联合或不联合先前化疗(n = 11)、放射治疗(n = 6)、细胞减灭化疗(n = 30)、轻度化疗(n = 27)或姑息治疗(n = 23),中位复发后总生存期(OS)分别为 10 个月、6.5 个月、3 个月、4 个月、4 个月和 1 个月。尽管在接受治疗的患者中,一线挽救治疗后的完全缓解率为 38%,但 OS 率仍然有限,1 年和 2 年的 OS 率分别为 17%(95%置信区间,13 至 29)和 10%(95%置信区间,6 至 20)。单因素分析显示,OS 的不良因素包括首次 HSCT 时疾病处于活动期和首次 HSCT 后进展时间短(<6 个月)。孤立性骨髓外复发(44%)与骨髓外和骨髓复发合并(29%)或孤立性骨髓复发(34%)患者的复发后 6 个月存活率无差异(P =.8)。我们的数据提供了更多关于 ALL 在 HSCT 后复发时疾病行为和治疗结果的深入了解,未来的试验可以进行比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b69/8439154/343d0a963850/nihms-1576619-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b69/8439154/343d0a963850/nihms-1576619-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b69/8439154/343d0a963850/nihms-1576619-f0001.jpg

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