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首页> 外文期刊>Journal of Clinical Oncology >T-cell-depleted reduced-intensity transplantation followed by donor leukocyte infusions to promote graft-versus-lymphoma activity results in excellent long-term survival in patients with multiply relapsed follicular lymphoma.
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T-cell-depleted reduced-intensity transplantation followed by donor leukocyte infusions to promote graft-versus-lymphoma activity results in excellent long-term survival in patients with multiply relapsed follicular lymphoma.

机译:T细胞耗竭的低强度移植,然后输注供体白细胞以促进移植物抗淋巴瘤活性,可导致多发性滤泡性淋巴瘤复发患者的出色长期生存。

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摘要

PURPOSE: Follicular lymphoma (FL) is an indolent disorder that is treatable but considered incurable with chemotherapy alone. The curative potential of allogeneic transplantation using conventional myeloablative conditioning has been demonstrated, but this approach is precluded in the majority of patients with FL because of excessive toxicity. Thus, reduced-intensity conditioning regimens are being explored. PATIENTS AND METHODS: This study reports the outcome of 82 consecutive patients with FL who underwent transplantation using fludarabine, melphalan, and alemtuzumab for in vivo T-cell depletion. Patients were heavily pretreated, having received a median of four lines of prior therapy, and 26% had experienced treatment failure with previous autologous transplantation. Median patient age was 45 years, and 52% of patients received stem cells from unrelated donors. RESULTS: With a median follow-up time of 43 months, the nonrelapse mortality was 15% at 4 years (8% for sibling and 22% for unrelated donor transplantations), acute grade 2 or 3 graft-versus-host disease (GVHD) occurred in 13%, and the incidence of extensive chronic GVHD was only 18%. Although relapse risk was 26%, this was significantly reduced where mixed chimerism had been converted to full donor chimerism by the use of donor lymphocyte infusion (DLI; P = .03). In addition, 10 (77%) of 13 patients given DLI for relapse after transplantation experienced remission, with nine of these responses being sustained. Current progression-free survival at 4 years was 76% for the whole cohort (90% for those with sibling donors and 64% for those with unrelated donors). CONCLUSION: The excellent long-term survival with associated low rates of GVHD and the frequency and durability of DLI responses make this an extremely encouraging strategy for the treatment and potential cure of FL.
机译:目的:滤泡性淋巴瘤(FL)是一种惰性疾病,可以治愈,但仅用化学疗法即可治愈。已经证明了使用常规的清髓疗法进行同种异体移植的治愈潜力,但是由于过度的毒性,这种方法在大多数FL患者中被排除。因此,正在研究降低强度的调节方案。病人和方法:本研究报告了82例连续的FL患者的结果,这些患者使用氟达拉滨,美法仑和阿仑单抗进行了体内T细胞耗竭移植。患者接受了严格的预处理,接受过之前四次中线的治疗,而26%的患者曾经历过自体移植的治疗失败。患者中位年龄为45岁,其中52%的患者接受了无关供体的干细胞。结果:平均随访时间为43个月,在4年时非复发死亡率为15%(同胞为8%,无关的供体移植为22%),急性2或3级移植物抗宿主病(GVHD)发生率为13%,广泛的慢性GVHD发生率仅为18%。尽管复发风险为26%,但在通过使用供体淋巴细胞输注将混合嵌合体转化为完全供体嵌合体的情况下,这种风险显着降低(DLI; P = .03)。此外,在接受移植后DLI复发的13例患者中,有10例(77%)缓解了,其中9例得以持续。目前,整个队列的4年无进展生存率为76%(同胞供者为90%,无亲缘供者为64%)。结论:GVHD的低发生率以及DLI反应的频率和持久性均具有出色的长期生存能力,这使其成为治疗和潜在治愈FL的极为令人鼓舞的策略。

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