酪氨酸激酶抑制剂预处理费城染色体阳性急性淋巴细胞白血病(Ph+ALL)非相关骨髓移植的预后因素和结果

Osaka city medical journal Pub Date : 2013-06-01
Takuro Yoshimura, Takahiko Nakane, Asao Hirose, Hideo Koh, Mika Nakamae, Mizuki Aimoto, Mitsutaka Nishimoto, Yoshiki Hayashi, Yoshiki Terada, Hirohisa Nakamae, Masayuki Hino
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引用次数: 0

摘要

背景:随着酪氨酸激酶抑制剂(TKIs)的引入,急性淋巴细胞白血病(ALL)的治疗和预后发生了变化,包括费城染色体阳性ALL (Ph+ALL)这一不良预后因素。尽管如此,同种异体造血细胞移植(allo-HCT)仍被推荐作为一线治疗方法。迄今为止,还没有研究调查非相关性骨髓移植(u-BMT)在移植前使用含tki方案治疗Ph+ALL后的预后因素和结果。方法:我们回顾性评估了14例Ph+ALL患者的15例移植手术,这些患者在我们研究所接受了含tki的治疗方案。14例患者男11例,女3例,中位年龄50岁(范围19-64岁)。我们对影响总生存期(OS)或无白血病生存期(LFS)的危险因素进行了单因素和多因素分析。结果:移植时分子完全缓解(MCR)和非MCR患者的3年OS分别为89%和40% (p = 0.006), 3年LFS分别为79%和0% (p = 0.001)。单因素分析显示,移植时首次血液学完全缓解(HCR1)和MCR与更好的OS和LFS显著相关。多因素分析显示,移植时的MCR与更好的OS和LFS显著相关。结论:与先前包括其他干细胞来源的研究一致,u-BMT被认为是治疗Ph+ALL的可行方法。需要对更大的队列进行分析,以阐明自引入TKIs以来影响Ph+ALL移植结果的预后因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic factors and outcomes of unrelated bone marrow transplantation for Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ALL) pre-treated with tyrosine kinase inhibitors.

Background: The treatment and prognosis of Acute Lymphoblastic Leukemia (ALL), including Philadelphia chromosome positive ALL (Ph+ALL), a poor prognostic factor, has changed with the introduction of tyrosine kinase inhibitors (TKIs). Nevertheless, allogeneic hematopoietic cell transplantation (allo-HCT) is still recommended as the first-line curative treatment. To date, no study has investigated the prognostic factors and outcomes of unrelated bone marrow transplantation (u-BMT) for Ph+ALL following pre-transplant treatment with a TKI-containing regimen.

Methods: We retrospectively evaluated 15 transplantations of 14 patients with Ph+ALL pre-treated with a TKI-containing regimen at our institute. The 14 patients comprised 11 males and 3 females, with a median age of 50 years (range: 19-64). We performed univariate and multivariate analyses of risk factors that contributed to overall survival (OS) or leukemia-free survival (LFS).

Results: Three-year OS of the patients with molecular complete remission (MCR) and with non-MCR at transplantation were 89% and 40% (p = 0.006), respectively, and three-year LFS rates were 79% and 0% (p = 0.001), respectively. Univariate analysis revealed that first hematological complete remission (HCR1) and MCR at transplant were significantly related to better OS and LFS. Multivariate analysis showed that MCR at transplant was significantly associated with better OS and LFS.

Conclusions: In agreement with a previous study that included other stem cell sources, u-BMT was deemed feasible for the treatment of Ph+ALL. Analysis of a larger cohort is required to clarify the prognostic factors that affect transplant outcome in Ph+ALL since the introduction of TKIs.

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