首页> 外文期刊>Bone marrow transplantation >Nilotinib restores long-term full-donor chimerism in Ph-positive acute lymphoblastic leukemia relapsed after allogeneic transplantation.
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Nilotinib restores long-term full-donor chimerism in Ph-positive acute lymphoblastic leukemia relapsed after allogeneic transplantation.

机译:尼洛替尼恢复了异基因移植后复发的Ph阳性急性淋巴细胞白血病的长期全供体嵌合。

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摘要

The prognosis of adult patients with Ph chromosome-positive ALL (Ph+ ALL) is considered poor with an expected long-term survival of 20% at 10 years while no patients with less than a 3-log reduction in BCR-ABL transcripts were alive at 2 years.1 The combination of imatinib with chemotherapy in the induction therapy regimen had improved the response rate, but had not affected overall survival.2 Allo-SCT is still considered the treatment of choice in adults with this disease, despite the fact that post-SCT relapses are relatively frequent.3 A second allotransplant is rarely successful. Administration of imatinib early after SCT might be an effective approach to prevent recurrence of Ph + ALL, but its feasibility has not been systematically evaluated.4 Second generation-targeted therapies, such as nilotinib (Novartis) and dasatinib (Bristol-Myers Squibb), have been evaluated for Ph+ ALL.5 Nilotinib monotherapy exhibits clinical activity in patients with relapsed/refractory Ph+ ALL with 26% achieving complete hematologic response (median treatment duration 1.8 months)6 while 31% achieved complete hematologic response with dasatinib (follow-up 6 months).
机译:成人成年Ph染色体阳性ALL(Ph + ALL)患者的预后较差,预计其10年的长期存活率可达20%,而BCR-ABL转录本减少不超过3-log的患者中尚无存活的方法。 2年。1在诱导治疗方案中伊马替尼与化学疗法的联合使用可提高缓解率,但并未影响整体生存率。2尽管在术后2个月,Allo-SCT仍被认为是该疾病成人的首选治疗方法。 -SCT复发相对频繁。3第二次同种异体移植很少成功。 SCT后早期给予伊马替尼可能是预防Ph + ALL复发的有效方法,但其可行性尚未得到系统评价。4第二代靶向疗法,如尼罗替尼(Novartis)和达沙替尼(Bristol-Myers Squibb),已对Ph + ALL进行了评估。5尼罗替尼单药治疗对复发/难治的Ph + ALL患者具有临床活性,其中26%达到完全血液学应答(中位治疗时间1.8个月)6,而31%达沙替尼实现完全血液学应答(随访6个月)。

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