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本文引用的文献

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Long-term follow-up of hematologic relapse-free survival in a phase 2 study of blinatumomab in patients with MRD in B-lineage ALL.在一项blinatumomab 治疗 B 系 ALL 患者微小残留病的 2 期研究中,血液学无复发生存的长期随访结果。
Blood. 2012 Dec 20;120(26):5185-7. doi: 10.1182/blood-2012-07-441030. Epub 2012 Sep 28.
2
Adult patients with acute lymphoblastic leukemia and molecular failure display a poor prognosis and are candidates for stem cell transplantation and targeted therapies.急性淋巴细胞白血病伴分子学复发的成年患者预后不良,是干细胞移植和靶向治疗的候选人群。
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Curing chronic myeloid leukemia.治愈慢性髓性白血病。
Curr Hematol Malig Rep. 2012 Jun;7(2):103-8. doi: 10.1007/s11899-012-0117-2.
4
Risk stratification-directed donor lymphocyte infusion could reduce relapse of standard-risk acute leukemia patients after allogeneic hematopoietic stem cell transplantation.风险分层指导下的供者淋巴细胞输注可降低异基因造血干细胞移植后标准风险急性白血病患者的复发率。
Blood. 2012 Apr 5;119(14):3256-62. doi: 10.1182/blood-2011-09-380386. Epub 2012 Feb 14.
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Active specific immunotherapy targeting the Wilms' tumor protein 1 (WT1) for patients with hematological malignancies and solid tumors: lessons from early clinical trials.针对血液系统恶性肿瘤和实体瘤患者的 Wilms 瘤蛋白 1(WT1)的主动特异性免疫治疗:来自早期临床试验的经验。
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6
Lymphodepletion is permissive to the development of spontaneous T-cell responses to the self-antigen PR1 early after allogeneic stem cell transplantation and in patients with acute myeloid leukemia undergoing WT1 peptide vaccination following chemotherapy.淋巴细胞耗竭允许在异基因干细胞移植后早期和化疗后接受 WT1 肽疫苗接种的急性髓系白血病患者中针对自身抗原 PR1 产生自发 T 细胞反应。
Cancer Immunol Immunother. 2012 Jul;61(7):1125-36. doi: 10.1007/s00262-011-1187-z. Epub 2011 Dec 24.
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Novel approaches to the treatment of acute myeloid leukemia.新型急性髓系白血病治疗方法。
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Long-term WT1 peptide vaccination for patients with acute myeloid leukemia with minimal residual disease.针对伴有微小残留病的急性髓系白血病患者的长期WT1肽疫苗接种。
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9
Differential impact of inhibitory and activating Killer Ig-Like Receptors (KIR) on high-risk patients with myeloid and lymphoid malignancies undergoing reduced intensity transplantation from haploidentical related donors.抑制性和激活性杀伤细胞免疫球蛋白样受体(KIR)对接受单倍体相合相关供者减强度移植的高危髓系和淋巴系恶性肿瘤患者的不同影响
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10
Adoptive immunotherapy with unselected or EBV-specific T cells for biopsy-proven EBV+ lymphomas after allogeneic hematopoietic cell transplantation.异基因造血细胞移植后,采用未经选择或 EBV 特异性 T 细胞进行活检证实的 EBV+淋巴瘤的过继免疫治疗。
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异基因干细胞移植后控制微小残留病的新方法。

New approaches to manipulate minimal residual disease after allogeneic stem cell transplantation.

作者信息

Rein Lindsay Am, Sung Anthony D, Rizzieri David A

机构信息

Division of Hematologic Malignancies & Cellular Therapy, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Int J Hematol Oncol. 2013 Feb;2(1). doi: 10.2217/ijh.13.4.

DOI:10.2217/ijh.13.4
PMID:24303095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3841006/
Abstract

Minimal residual disease (MRD) is a complex topic that has been studied extensively in hematologic malignancies given its clinical implications related to prognosis. However, methods to monitor and treat MRD, especially after stem cell transplantation, are not well defined and vary in different disease processes. Alternative transplant strategies, such as reduced-intensity conditioning, have altered the way we assess and address MRD after transplantation. Development of new diagnostic tools have allowed for higher sensitivity and specificity of testing. Both targeted chemotherapeutic agents and immunotherapies have been developed to treat MRD in hopes of improving patient outcomes. This article aims to address ways to define and manipulate MRD specifically after stem cell transplantation.

摘要

微小残留病(MRD)是一个复杂的话题,鉴于其与预后相关的临床意义,已在血液系统恶性肿瘤中得到广泛研究。然而,监测和治疗MRD的方法,尤其是在干细胞移植后,尚未明确界定,且在不同的疾病过程中有所不同。替代移植策略,如减低强度预处理,改变了我们在移植后评估和处理MRD的方式。新诊断工具的开发提高了检测的灵敏度和特异性。靶向化疗药物和免疫疗法均已用于治疗MRD,以期改善患者预后。本文旨在探讨干细胞移植后明确和控制MRD的方法。