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成年混合表型急性白血病患者的异基因造血干细胞移植:配对分析结果

Allogeneic hematopoietic stem cell transplantation for adult patients with mixed phenotype acute leukemia: results of a matched-pair analysis.

作者信息

Shimizu Hiroaki, Saitoh Takayuki, Machida Shinichiro, Kako Shinichi, Doki Noriko, Mori Takehiko, Sakura Toru, Kanda Yoshinobu, Kanamori Heiwa, Miyawaki Shuichi, Okamoto Shinichiro

机构信息

Department of Medicine and Clinical Science, Gunma University, Gunma, Japan.

Department of Hematology and Oncology, Tokai University School of Medicine, Kanagawa, Japan.

出版信息

Eur J Haematol. 2015 Nov;95(5):455-60. doi: 10.1111/ejh.12516. Epub 2015 Mar 13.

Abstract

Adult patients with mixed phenotype acute leukemia (MPAL) have a poor prognosis, and the therapeutic role of allogeneic stem cell transplantation (allo-SCT) for MPAL remains to be elucidated. Thus, we retrospectively assessed the efficacy of allo-SCT for MPAL. Eighteen patients with MPAL were identified from the transplant outcome database of Kanto Study Group for Cell Therapy (KSGCT). We also selected 215 patients with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) as control cohorts using an optimal matching method. The 5-yr overall survival (OS) rate of patients with MPAL was 48.1%, and patients in remission at the time of transplant showed significantly better survival than those not in remission (5-yr OS: 71.8% vs. 0%, P = 0.001). No significant differences were seen in OS when stratifying patients according to immunophenotype, cytogenetic abnormalities, or the type of induction therapy. The 5-yr OS rate of patients with MPAL was not significantly different compared with AML control patients (48.1% vs. 48.1%; P = 0.855) or ALL control patients (48.1% vs. 37.8%; P = 0.426). These results suggested that allo-SCT is an effective treatment for MPAL, especially early in the disease course, and innovative transplant approaches are warranted to improve the transplant outcome of patients with MPAL who are not in remission.

摘要

混合表型急性白血病(MPAL)成年患者预后较差,异基因干细胞移植(allo-SCT)对MPAL的治疗作用仍有待阐明。因此,我们回顾性评估了allo-SCT治疗MPAL的疗效。从关东细胞治疗研究组(KSGCT)的移植结果数据库中确定了18例MPAL患者。我们还采用最佳匹配方法选择了215例急性髓系白血病(AML)和急性淋巴细胞白血病(ALL)患者作为对照队列。MPAL患者的5年总生存率(OS)为48.1%,移植时处于缓解期的患者生存率明显高于未缓解患者(5年OS:71.8%对0%,P = 0.001)。根据免疫表型、细胞遗传学异常或诱导治疗类型对患者进行分层时,OS无显著差异。MPAL患者的5年OS率与AML对照患者(48.1%对48.1%;P = 0.855)或ALL对照患者(48.1%对37.8%;P = 0.426)相比无显著差异。这些结果表明,allo-SCT是治疗MPAL的有效方法,尤其是在病程早期,有必要采用创新的移植方法来改善未缓解的MPAL患者的移植结局。

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