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伊马替尼联合化疗成功治疗异基因骨髓移植后复发的费城染色体阳性急性淋巴细胞白血病。

Successful treatment with imatinib-combined chemotherapy for relapsed Philadelphia-positive acute lymphoblastic leukemia after allogeneic bone marrow transplantation.

作者信息

IMAHASHI Nobuhiko, TOKUNAGA Masahiro, NISHIWAKI Satoshi, YANAGISAWA Mayumi, OZAWA Yukiyasu, MIYAMURA Koichi

机构信息

Department of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya.

出版信息

Rinsho Ketsueki. 2009 Nov;50(11):1612-5.

Abstract

The prognosis of patients with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph(+)ALL) relapsing after allogeneic hematopoietic stem cell transplantation is dismal. Here we describe a patient with post-transplant relapse of Ph(+)ALL, who has remained in complete remission (CR) for 30 months after relapse. A 55-year-old woman with Ph(+)ALL received allo-HSCT from an unrelated donor during first CR. The conditioning regimen consisted of fludarabine+melphalan, and graft-versus-host disease (GVHD) prophylaxis consisted of tacrolimus and short-term methotrexate. She achieved and maintained molecular remission without developing GVHD after transplantation, but suffered a hematologic relapse on day 871. She received imatinib-combined chemotherapy, and again achieved molecular remission. Since the completion of imatinib-combined chemotherapy, she has been receiving imatinib monotherapy. Although it has been reported that chemotherapy and imatinib are effective only transiently in patients with relapsed Ph(+)ALL, our patient has remained in molecular remission for 30 months after post-transplant relapse at the time of this report. Our case suggests that by continuing imatinib after the induction of molecular remission by imatinib-combined chemotherapy, the antileukemic activity of imatinib could achieve durable remission in combination with the graft-versus-leukemia effect. However, this needs to be investigated in studies involving a large number of patients.

摘要

费城染色体阳性急性淋巴细胞白血病(Ph(+)ALL)患者在异基因造血干细胞移植后复发,其预后很差。在此,我们描述一名Ph(+)ALL移植后复发的患者,该患者在复发后已持续完全缓解(CR)30个月。一名55岁的Ph(+)ALL女性患者在首次完全缓解期接受了来自无关供者的异基因造血干细胞移植。预处理方案为氟达拉滨+美法仑,移植物抗宿主病(GVHD)预防方案为他克莫司和短期甲氨蝶呤。移植后她实现并维持了分子学缓解,且未发生GVHD,但在第871天出现血液学复发。她接受了伊马替尼联合化疗,并再次实现分子学缓解。自伊马替尼联合化疗结束后,她一直在接受伊马替尼单药治疗。尽管有报道称化疗和伊马替尼对复发的Ph(+)ALL患者仅能产生短暂疗效,但在本报告发布时,我们的患者在移植后复发后已保持分子学缓解30个月。我们的病例提示,在伊马替尼联合化疗诱导分子学缓解后继续使用伊马替尼,伊马替尼的抗白血病活性与移植物抗白血病效应相结合可实现持久缓解。然而,这需要在涉及大量患者的研究中进行调查。

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