首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >NCI First International Workshop on the Biology, Prevention, and Treatment of Relapse after Allogeneic Hematopoietic Stem Cell Transplantation: report from the Committee on the Epidemiology and Natural History of Relapse following Allogeneic Cell Transplantation.
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NCI First International Workshop on the Biology, Prevention, and Treatment of Relapse after Allogeneic Hematopoietic Stem Cell Transplantation: report from the Committee on the Epidemiology and Natural History of Relapse following Allogeneic Cell Transplantation.

机译:NCI首届国际同种异体造血干细胞移植后复发的生物学,预防和治疗研讨会:来自同种异体细胞移植后流行病学和复发自然史委员会的报告。

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Allogeneic hematopoietic stem cell transplantation (alloHSCT) is increasingly being used for treatment of hematologic malignancies, and the immunologic graft-versus-tumor effect (GVT) provides its therapeutic effectiveness. Disease relapse remains a cause of treatment failure in a significant proportion of patients undergoing alloHSCT without improvements over the last 2-3 decades. We summarize here current data and outline future research regarding the epidemiology, risk factors, and outcomes of relapse after alloHSCT. Although some factors (eg, disease status at alloHSCT or graft-versus-host disease [GVHD] effects) are common, other disease-specific factors may be unique. The impact of reduced-intensity regimens on relapse and survival still need to be assessed using contemporary supportive care and comparable patient populations. The outcome of patients relapsing after an alloHSCT generally remains poor even though interventions including donor leukocyte infusions can benefit some patients. Trials examining targeted therapies along with improved safety of alloHSCT may result in improved outcomes, yet selection bias necessitates prospective assessment to gauge the real contribution of any new therapies. Ongoing chronic GVHD (cGVHD) or other residual post-alloHSCT morbidities may limit the applicability of new therapies. Developing strategies to promptly identify patients as alloHSCT candidates, while malignancy is in a more treatable stage, could decrease relapses rates after alloHSCT. Better understanding and monitoring of minimal residual disease posttransplant could lead to novel preemptive treatments of relapse. Analyses of larger cohorts through multicenter collaborations or registries remain essential to probe questions not amenable to single center or prospective studies. Studies need to provide data with detail on disease status, prior treatments, biologic markers, and posttransplant events. Stringent statistical methods to study relapse remain an important area of research. The opportunities for improvement in prevention and management of post-alloHSCT relapse are apparent, but clinical discipline in their careful study remains important.
机译:同种异体造血干细胞移植(alloHSCT)越来越多地用于治疗血液系统恶性肿瘤,免疫移植物抗肿瘤效应(GVT)提供了治疗效果。在过去的2-3年中,相当大比例的接受alloHSCT的患者中疾病复发仍然是治疗失败的原因,但没有改善。我们在这里总结当前的数据,并概述有关alloHSCT后的流行病学,危险因素和复发结果的未来研究。尽管某些因素(例如,alloHSCT的疾病状态或移植物抗宿主病[GVHD]效应)是常见的,但其他疾病特异性因素可能是独特的。降低强度的疗法对复发和生存的影响仍然需要使用当代的支持治疗和可比较的患者人群进行评估。尽管包括供体白细胞输注在内的干预措施可使部分患者受益,但在同种异体造血干细胞移植后复发的患者的预后通常仍然较差。检验靶向疗法以及提高alloHSCT安全性的试验可能会改善疗效,但是选择偏倚需要前瞻性评估,以评估任何新疗法的真正贡献。持续的慢性GVHD(cGVHD)或其他alloHSCT后残留病态可能会限制新疗法的适用性。在恶性处于更可治疗的阶段时,制定策略以迅速将患者识别为同种异体造血干细胞移植候选者,可以降低同种异体造血干细胞移植术后的复发率。更好地理解和监测移植后的最小残留疾病可能会导致新的先发性复发治疗。通过多中心协作或注册中心进行的较大队列分析对于探究不适合单个中心或前瞻性研究的问题仍然至关重要。研究需要提供有关疾病状况,先前治疗,生物标志物和移植后事件的详细数据。研究复发的严格统计学方法仍然是重要的研究领域。改善alloHSCT后复发的预防和管理的机会是显而易见的,但是对其进行仔细研究的临床纪律仍然很重要。

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