首页> 美国卫生研究院文献>Annals of Oncology >A large single-center experience with allogeneic stem-cell transplantation for peripheral T-cell non-Hodgkin lymphoma and advanced mycosis fungoides/Sezary syndrome
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A large single-center experience with allogeneic stem-cell transplantation for peripheral T-cell non-Hodgkin lymphoma and advanced mycosis fungoides/Sezary syndrome

机译:同种异体干细胞移植治疗周围性T细胞非霍奇金淋巴瘤和晚期真菌病真菌/塞萨里综合征的大型单中心经验

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摘要

>Background: The prognosis for patients with most forms of T-cell lymphoma is poor. Allogeneic hematopoietic stem-cell transplantation (HSCT) may improve the outcome.>Patients and methods: This study examines the outcome of 52 patients who underwent ablative or nonablative allogeneic HSCT for peripheral T-cell lymphoma (PTCL) or advanced mycosis fungoides/Sezary syndrome over a 12-year period at a single institution. We divided the patients into those with predominantly nodal histologies: peripheral T-cell not otherwise specified (PTCL NOS), angioimmunoblastic (AITL), or anaplastic large cell lymphoma, Tull type (systemic) (ALCL), and predominantly extranodal histologies: natural killer (NK)/T cell, enteropathy type, hepatosplenic, subcutaneous panniculitic, mycosis fungoides, or T cell or NK cell other.>Results: Median follow-up of survivors is 49 months. Non-relapse mortality and relapse at 3 years was 27% and 43%, respectively. The incidence of grade II–IV acute graft-versus-host disease (GVHD) was 21%. The incidence of extensive chronic GVHD at 2 years was 27%. The 3-year progression-free survival was 30%: 45% in patients with predominantly nodal histologies (PTCL NOS, AITL, and ALCL) and 6% in patients with predominantly extranodal histologies (P = 0.016). Overall survival at 3 years was 41% for all patients.>Conclusion: Allogeneic HSCT can produce long-term remissions in relapsed/refractory T-cell lymphoma, especially those with nodal histologies.
机译:>背景:大多数形式的T细胞淋巴瘤患者的预后很差。同种异体造血干细胞移植(HSCT)可能会改善结局。>患者和方法:本研究检查了52例接受了周围性T细胞淋巴瘤(PTCL)切除或非切除性异体HSCT的患者的结果在单一机构中,患有真菌病晚期真菌/ Sezary综合征的时间长达12年。我们将患者分为以淋巴结为主的组织学:未另外指定的外周T细胞(PTCL NOS),血管免疫母细胞(AITL)或间变性大细胞淋巴瘤,T / null型(全身性)(ALCL)和以淋巴结外的组织学为主:自然杀伤(NK)/ T细胞,肠病类型,肝脾,皮下脂膜炎,真菌病或其他T细胞或NK细胞。>结果:幸存者的中位随访时间为49个月。 3年的非复发死亡率和复发率分别为27%和43%。 II–IV级急性移植物抗宿主病(GVHD)的发生率为21%。 2年时广泛性慢性GVHD的发生率为27%。 3年无进展生存率为30%:主要是淋巴结组织学(PTCL NOS,AITL和ALCL)的患者为45%,主要是淋巴结外组织学的患者为6%(P = 0.016)。所有患者在3年时的总生存率为41%。>结论:同种异体HSCT可以使复发/难治性T细胞淋巴瘤(尤其是结节性组织学)长期缓解。

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