Allogeneic hematopoietic cell transplantation in adult acute myeloid leukemia with 11q23 abnormality: a retrospective study of the Adult Acute Myeloid Leukemia Working Group of the Japan Society for Hematopoietic Cell Transplantation (JSHCT)

被引:0
作者
Takaaki Konuma
Shohei Mizuno
Tadakazu Kondo
Hiroki Yamaguchi
Takahiro Fukuda
Naoyuki Uchida
Yuho Najima
Heiwa Kanamori
Shuichi Ota
Hirohisa Nakamae
Mika Nakamae
Ishikazu Mizuno
Junichi Sugita
Yasushi Onishi
Akira Yokota
Satoshi Takahashi
Yoshinobu Kanda
Tatsuo Ichinohe
Yoshiko Atsuta
Shingo Yano
机构
[1] The University of Tokyo,Department of Hematology/Oncology, The Institute of Medical Science
[2] Aichi Medical University,Division of Hematology, Department of Internal Medicine, School of Medicine
[3] Kyoto University,Department of Hematology and Oncology, Graduate School of Medicine
[4] Nippon Medical School,Department of Hematology
[5] National Cancer Center Hospital,Department of Hematopoietic Stem Cell Transplantation
[6] Federation of National Public Service Personnel Mutual Aid Associations Toranomon Hospital,Department of Hematology
[7] Komagome Hospital,Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center
[8] Kanagawa Cancer Center,Department of Hematology
[9] Sapporo Hokuyu Hospital,Department of Hematology
[10] Osaka City University,Hematology, Graduate School of Medicine
[11] Hyogo Cancer Center,Department of Hematology
[12] Hokkaido University Graduate School of Medicine,Department of Hematology
[13] Tohoku University Hospital,Department of Hematology and Rheumatology
[14] Chiba Aoba Municipal Hospital,Department of Hematology
[15] The University of Tokyo,Division of Molecular Therapy, The Advanced Clinical Research Center, The Institute of Medical Science
[16] Jichi Medical University,Division of Hematology
[17] Saitama Medical Center,Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine
[18] Hiroshima University,Department of Healthcare Administration
[19] Japanese Data Center for Hematopoietic Cell Transplantation,Division of Clinical Oncology and Hematology, Department of Internal Medicine
[20] Nagoya University Graduate School of Medicine,undefined
[21] Jikei University School of Medicine,undefined
来源
Annals of Hematology | 2018年 / 97卷
关键词
11q23 abnormality; Mixed lineage leukemia; Lysine-specific methyltransferase 2A; Acute myeloid leukemia; Allogeneic hematopoietic cell transplantation; Minimal residual disease; Adult;
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学科分类号
摘要
An 11q23 abnormality presents in approximately 5% of adults with acute myeloid leukemia (AML) and is associated with adverse outcomes even after allogeneic hematopoietic cell transplantation (allo-HCT). To evaluate the outcomes and prognostic factors following allo-HCT for adult AML with 11q23 abnormality, we retrospectively analyzed the Japanese registration data of 322 adult AML patients with 11q23 abnormality who had received allo-HCT between 1990 and 2014. In total, the disease status at HCT was first complete remission (CR1) in 159 (49%) patients. The probability of overall survival and the cumulative incidence of relapse at 3 years were 44 and 44%, respectively. In the multivariate analysis, disease status beyond CR1 at the time of HCT was significantly associated with a higher overall mortality and relapse. The 11q23 fusion partner did not have a significant impact on survival. We also evaluated the prognostic value of minimal residual disease (MRD) status at HCT on transplant outcomes among hematological CR patients. MRD status at HCT was the significant prognostic indicator for hematological relapse and survival. These data suggested that allo-HCT offered a curative option for adult AML with 11q23 abnormality. Pretransplant MRD status was the significant prognostic indicator for relapse and survival in CR patients.
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页码:2173 / 2183
页数:10
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  • [1] Slovak ML(2000)Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: a Southwest Oncology Group/Eastern Cooperative Oncology Group Study Blood 96 4075-4083
  • [2] Kopecky KJ(2002)Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B (CALGB 8461) Blood 100 4325-4336
  • [3] Cassileth PA(2010)Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials Blood 116 354-365
  • [4] Harrington DH(2017)Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel Blood 129 424-447
  • [5] Theil KS(2002)The value of allogeneic bone marrow transplant in patients with acute myeloid leukaemia at differing risk of relapse: results of the UK MRC AML 10 trial Br J Haematol 118 385-400
  • [6] Mohamed A(2007)Impact of cytogenetics on outcome of matched unrelated donor hematopoietic stem cell transplantation for acute myeloid leukemia in first or second complete remission Blood 110 409-417
  • [7] Paietta E(2007)Impact of Cytogenetics on Outcome of De Novo and Therapy-Related AML and MDS after Allogeneic Transplantation Biology of Blood and Marrow Transplantation 13 655-664
  • [8] Willman CL(2012)Classifying cytogenetics in patients with acute myelogenous leukemia in complete remission undergoing allogeneic transplantation: a center for international blood and marrow transplant research study Biol Blood Marrow Transplant 18 280-288
  • [9] Head DR(1997)Adult patients with de novo acute myeloid leukemia and t(9; 11)(p22; q23) have a superior outcome to patients with other translocations involving band 11q23: a cancer and leukemia group B study Blood 90 4532-4538
  • [10] Rowe JM(2009)Prognostic factors in adult patients up to 60 years old with acute myeloid leukemia and translocations of chromosome band 11q23: individual patient data-based meta-analysis of the German Acute Myeloid Leukemia Intergroup J Clin Oncol 27 3000-3006