Donor lymphocyte infusion after haploidentical hematopoietic stem cell transplantation for acute myeloid leukemia

被引:0
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作者
Kaito Harada
Shohei Mizuno
Shingo Yano
Akiyoshi Takami
Hiroto Ishii
Kazuhiro Ikegame
Yuho Najima
Shinichi Kako
Takashi Ashida
Souichi Shiratori
Shuichi Ota
Makoto Onizuka
Kentaro Fukushima
Takahiro Fukuda
Tatsuo Ichinohe
Yoshiko Atsuta
Masamitsu Yanada
机构
[1] Tokai University School of Medicine,Department of Hematology and Oncology
[2] Aichi Medical University,Division of Hematology, Department of Internal Medicine
[3] The Jikei University School of Medicine,Clinical Oncology and Hematology
[4] Hyogo College of Medicine Hospital,Department of Hematology
[5] Komagome Hospital,Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center
[6] Jichi Medical University Saitama Medical Center,Division of Hematology
[7] Kinki University Hospital,Division of Hematology and Rheumatology, Department of Internal Medicine
[8] Hokkaido University Hospital,Department of Hematology
[9] Sapporo Hokuyu Hospital,Department of Hematology
[10] Osaka University Graduate School of Medicine,Department of Hematology and Oncology
[11] National Cancer Center Hospital,Hematopoietic Stem Cell Transplantation Division
[12] Hiroshima University,Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine
[13] Japanese Data Center for Hematopoietic Cell Transplantation,Department of Healthcare Administration
[14] Nagoya University Graduate School of Medicine,Department of Hematology and Cell Therapy
[15] Aichi Cancer Center,undefined
来源
Annals of Hematology | 2022年 / 101卷
关键词
Acute myeloid leukemia; Donor lymphocyte infusion; Haploidentical stem cell Transplantation; Cell therapy;
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摘要
Although haploidentical donor lymphocyte infusion (DLI) is a valid treatment option for relapsed acute myeloid leukemia (AML), the incidence and risk factors for graft-versus-host disease (GVHD) and the efficacy of haploidentical DLI have not been fully evaluated. We retrospectively analyzed the outcomes after haploidentical DLI for 84 patients with AML using a nationwide database and additional questionnaires. The median number of DLI cycles and infused CD3+ cell dose was 1 and 1.0 × 106/kg, respectively. The infused CD3+ cell count of 5.0 × 105/kg or higher was associated with acute GVHD (grade II–IV, 32.1% vs. 10.5%, p = 0.03; grade III–IV, 21.4% vs. 5.3%, p = 0.10). Patients who developed grade III–IV acute GVHD more frequently succumbed to treatment-related mortality (46.7% vs. 15.8% at 1 year, p = 0.002), although the relapse-related mortality was significantly low (40.0% vs. 72.2% at 1 year, p = 0.025). The overall response to DLI was significantly higher in the preemptive DLI group (47.4%) than in the therapeutic group (13.9%, p = 0.002). In the multivariate analysis, preemptive DLI was the predictive factor for overall response (odds ratio, 5.58; p = 0.003). Our results indicated the substantial risk of acute GVHD after haploidentical DLI with CD3+ cell count of 5.0×105/kg or higher and the favorable outcomes after preemptive DLI.
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页码:643 / 653
页数:10
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