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移植后伊马替尼给药对费城染色体阳性急性淋巴细胞白血病的影响。

Impact of post-transplant imatinib administration on Philadelphia chromosome-positive acute lymphoblastic leukaemia.

机构信息

Department of Hematology, Japanese Red Cross Nagoya First Hospital, 3-35 Michishita-cho, Nakamura-ku, Nagoya 453-8511, Japan.

出版信息

Anticancer Res. 2010 Jun;30(6):2415-8.

Abstract

To evaluate the effect of post-transplant imatinib administration, 34 Philadelphia chromosome-positive acute lymphoblastic leukaemia (Ph(+)ALL) patients were retrospectively analysed, with 7 receiving post-transplant imatinib administration. Overall survival was significantly better in patients with post-transplant administration (66.7% vs. 29.6% at 3 years, p=0.03), with no significant difference in leukaemia-free survival (0% vs. 29.6% at 3 years, p=0.29). The median duration of negative minimal residual disease (MRD) in patients with post-transplant imatinib administration was 6 months in the pre-emptive administration group, where imatinib was administered upon detecting MRD after allogeneic stem cell transplantation (allo-SCT). In the prophylactic administration group, imatinib was administered as soon as possible after allo-SCT, and the median duration of MRD was 12 months. In all patients whose observation periods were longer than one year, MRD became positive in both groups leading to haematological relapse. It is therefore concluded that post-transplant imatinib administration is not an ideal treatment for Ph(+)ALL patients whose MRD is positive at allo-SCT.

摘要

为了评估移植后伊马替尼给药的效果,回顾性分析了 34 例费城染色体阳性急性淋巴细胞白血病(Ph(+)ALL)患者,其中 7 例接受了移植后伊马替尼给药。移植后给药患者的总生存率明显更好(3 年时为 66.7% vs. 29.6%,p=0.03),无白血病无进展生存率无显著差异(3 年时为 0% vs. 29.6%,p=0.29)。在移植后伊马替尼给药组中,有预先给药组和预防给药组,前者在异基因干细胞移植(allo-SCT)后检测到 MRD 时即开始给予伊马替尼,后者在 allo-SCT 后尽快给予伊马替尼。在预先给药组中,中位阴性微小残留病(MRD)持续时间为 6 个月,在预防给药组中,中位 MRD 持续时间为 12 个月。所有观察期超过一年的患者,两组的 MRD 均转为阳性,导致血液学复发。因此,对于 allo-SCT 时 MRD 阳性的 Ph(+)ALL 患者,移植后伊马替尼给药不是一种理想的治疗方法。

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