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酪氨酸激酶抑制剂时代加速期或急变期慢性髓性白血病儿童骨髓移植后的结局

Outcomes Following Bone Marrow Transplantation in Children With Accelerated Phase or Blast Crisis Chronic Myelogenous Leukemia in the Era of Tyrosine Kinase Inhibitors.

作者信息

Shulman David S, Lee Michelle A, Lehmann Leslie E, Margossian Steven P

机构信息

*Boston Children's Hospital †Pediatric Stem Cell Transplantation Center, Dana-Farber Cancer Institute/Boston Children's Hospital, Boston, MA.

出版信息

J Pediatr Hematol Oncol. 2016 Nov;38(8):610-614. doi: 10.1097/MPH.0000000000000636.

Abstract

The management of chronic myelogenous leukemia (CML) in children changed dramatically with the introduction of tyrosine kinase inhibitors (TKIs). Unfortunately, outcomes for patients presenting in an advanced stage-accelerated phase or blast crisis CML-continues to be poor, requiring chemotherapy and allogeneic hematopoietic stem cell transplant (HSCT) to attempt cure. Integration of TKIs in the therapy of advanced CML is still an area of active investigation. There are little published data on TKI use in children with advanced stage CML. We performed a retrospective review of all children treated at our institution between January 1, 2010 and June 30, 2013, and identified 5 children, age 12 to 18 years, with advanced stage CML. All patients were treated with a TKI before HSCT and TKIs were restarted post-HSCT in 4/5 with a goal of continuing until 2 years posttransplant. At time of HSCT all were in a morphologic and cytogenetic remission; 1 patient had also achieved molecular remission. All patients are alive and in molecular remission at an average of 38 months (range, 14 to 51 mo) following transplant. Our experience indicates that TKIs are safe and well tolerated in children both pretransplant and posttransplant and may improve outcomes in this aggressive disease.

摘要

随着酪氨酸激酶抑制剂(TKIs)的引入,儿童慢性粒细胞白血病(CML)的治疗发生了巨大变化。不幸的是,处于晚期(加速期或急变期CML)的患者预后仍然很差,需要化疗和异基因造血干细胞移植(HSCT)来尝试治愈。将TKIs整合到晚期CML的治疗中仍是一个积极研究的领域。关于TKIs在晚期CML儿童中的应用, published data很少。我们对2010年1月1日至2013年6月30日期间在我们机构接受治疗的所有儿童进行了回顾性研究,确定了5名年龄在12至18岁之间的晚期CML儿童。所有患者在HSCT前均接受了TKI治疗,4/5的患者在HSCT后重新开始使用TKI,目标是持续到移植后2年。在进行HSCT时,所有患者均处于形态学和细胞遗传学缓解状态;1例患者也达到了分子学缓解。所有患者在移植后平均38个月(范围14至51个月)时均存活且处于分子学缓解状态。我们的经验表明,TKIs在儿童移植前和移植后都是安全且耐受性良好的,并且可能改善这种侵袭性疾病的预后。

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