Yoshimura Takuro, Nakane Takahiko, Hirose Asao, Koh Hideo, Nakamae Mika, Aimoto Mizuki, Nishimoto Mitsutaka, Hayashi Yoshiki, Terada Yoshiki, Nakamae Hirohisa, Hino Masayuki
Department of Hematology, Osaka City University, Graduate School of Medicine, Japan.
Osaka City Med J. 2013 Jun;59(1):9-21.
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.
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).
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.
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.
急性淋巴细胞白血病(ALL)的治疗和预后,包括预后不良因素费城染色体阳性ALL(Ph+ALL),随着酪氨酸激酶抑制剂(TKIs)的引入而发生了变化。尽管如此,异基因造血细胞移植(allo-HCT)仍被推荐作为一线根治性治疗方法。迄今为止,尚无研究调查在移植前采用含TKI方案治疗后的Ph+ALL患者进行非亲缘骨髓移植(u-BMT)的预后因素和结局。
我们回顾性评估了我院14例接受含TKI方案预处理的Ph+ALL患者的15次移植情况。这14例患者包括11例男性和3例女性,中位年龄为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。
移植时分子完全缓解(MCR)和非MCR患者的3年总生存率分别为89%和40%(p = 0.006),3年无白血病生存率分别为79%和0%(p = 0.001)。单因素分析显示,首次血液学完全缓解(HCR1)和移植时的MCR与更好的OS和LFS显著相关。多因素分析表明,移植时的MCR与更好的OS和LFS显著相关。
与之前一项纳入其他干细胞来源的研究一致,u-BMT被认为可用于治疗Ph+ALL。由于TKIs的引入,需要分析更大的队列以明确影响Ph+ALL移植结局的预后因素。