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Allogeneic stem cell transplantation in the management of acute myeloid leukemia

机译:同种异体干细胞移植治疗急性粒细胞白血病

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Allogeneic stem cell transplantation (SCT) is the most powerful treatment option for acute myeloid leukemia (AML). However, SCT is also complicated by a high risk for treatment-related morbidity and mortality. The antileukemic effect of SCT is based on the radio-/chemotherapy applied for conditioning, as well as on the allogeneic immune reaction, mediated by immunocompetent donor cells, the graft-versus-leukemia effect. The latter effect is of particular importance in the context of reduced-intensity conditioning regimens, that have enabled us to offer allogeneic SCT to a by far bigger part of patients suffering from AML. The indication for allogeneic SCT is based on the patient's individual risk profile. Biological and clinical characteristics of the leukemia contribute to this risk profile, as do extraleukemic conditions such as age and comorbidity. Allogeneic SCT represents the standard of care for all patients with AML < 65 years of age, who are beyond first complete remission (CR) or who have failed to respond to induction chemotherapy. In first CR, allogeneic SCT is a standard for patients with unfavorable karyotype disease or other risk factors, whereas for patients without specific risk factors it is just an option, in particular within clinical trials. In patients with a favorable leukemic karyotype, allogeneic SCT is usually not performed in first CR. Future developments in the field include transplant strategies specifically designed for biological AML subgroups, as well as the integration of new drugs into transplant regimens.
机译:同种异体干细胞移植(SCT)是急性髓细胞性白血病(AML)的最强大的治疗选择。但是,SCT还因与治疗相关的发病率和死亡率高风险而变得复杂。 SCT的抗白血病作用基于用于适应性治疗的放射/化学疗法,以及基于具有免疫能力的供体细胞介导的同种异体免疫反应,即移植物抗白血病作用。在降低强度的调节方案的背景下,后一种效果尤其重要,这使我们能够向绝大部分患有AML的患者提供同种异体SCT。异基因SCT的适应症基于患者的个人风险状况。白血病的生物学和临床特征以及诸如年龄和合并症之类的白血病外疾病也导致了这种风险。同种异体SCT代表了所有小于65岁的AML,首次完全缓解(CR)超出或对诱导化疗没有反应的患者的护理标准。在第一个CR中,同种异体SCT是具有不利核型疾病或其他危险因素的患者的标准,而对于没有特定危险因素的患者,这只是一个选择,尤其是在临床试验中。对于具有良好白血病核型的患者,异基因SCT通常不会在首次CR中进行。该领域的未来发展包括专门为生物学AML亚组设计的移植策略,以及将新药整合到移植方案中。

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