首页> 美国卫生研究院文献>Case Reports in Hematology >Persistent Mixed Donor Chimerism following Double Umbilical Cord Transplantation in a Patient with T-Cell Prolymphocytic Leukemia
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Persistent Mixed Donor Chimerism following Double Umbilical Cord Transplantation in a Patient with T-Cell Prolymphocytic Leukemia

机译:T细胞淋巴细胞性白血病患者双脐带移植后的持久性混合供体嵌合。

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摘要

T-cell prolymphocytic leukemia (T-PLL) is a rare and aggressive postthymic T-cell neoplasm with an associated survival time of 1 year when left untreated. Current standard of care for T-PLL is with alemtuzumab, followed by allogeneic or autologous stem cell transplant. Little is found in the literature about alternative donor transplantation in T-PLL. Here, we present the case of a patient treated with double umbilical cord blood transplantation, which resulted in initial complete remission. An unusual outcome of this case is that coengraftment of both cords was established. After 16 months, the patient had relapse of the disease, unfortunately, prompting treatment with alemtuzumab and pentostatin, which resulted in remission once again. Here, we report a unique phenomenon whereby single-cord dominance occurred after treatment with these agents, suggesting that anti-T-cell therapy after transplant may help achieve single-unit dominance. A second relapse of the disease occurred six months thereafter, ultimately resulting in the patient's death, highlighting the aggressive nature of this disease.
机译:T细胞淋巴细胞性白血病(T-PLL)是一种罕见的侵袭性胸腺后T细胞肿瘤,如果不治疗,其相关生存时间为1年。 T-PLL的当前护理标准是使用alemtuzumab,然后进行异体或自体干细胞移植。在关于T-PLL的供体替代移植的文献中几乎找不到。在此,我们介绍了接受双脐带血移植治疗的患者的情况,该患者导致最初的完全缓解。这种情况的不寻常结果是建立了两个脐带的共移植。 16个月后,不幸的是该患者复发了该病,促使其使用Alemtuzumab和pentostatin进行治疗,从而再次缓解了病情。在这里,我们报道了一种独特的现象,即在使用这些药物治疗后单线优势占优势,这表明移植后的抗T细胞疗法可能有助于实现单单元优势。此病六个月后第二次复发,最终导致患者死亡,凸显了这种疾病的侵略性。

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