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对于 55 岁及以上的血液恶性肿瘤患者,作为根治性治疗的异基因造血干细胞移植中,T 细胞耗竭是一种替代方法。

T Cell Depletion as an Alternative Approach for Patients 55 Years or Older Undergoing Allogeneic Stem Cell Transplantation as Curative Therapy for Hematologic Malignancies.

机构信息

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; Weill Cornell Medical College, Cornell University, New York, New York.

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

Biol Blood Marrow Transplant. 2017 Oct;23(10):1685-1694. doi: 10.1016/j.bbmt.2017.06.024. Epub 2017 Jul 19.

Abstract

T cell-depleted (TCD) allogeneic hematopoietic stem cell transplantation (HSCT) is curative treatment for hematologic malignancies in adults, shown to reduce graft-versus-host disease (GVHD) without increased relapse. We retrospectively reviewed a single-center, 11-year experience of 214 patients aged ≥ 55 years to determine tolerability and efficacy in the older adult. Most patients (70%) had myeloid diseases, and most acute leukemias were in remission. Median age was 61 years, with related and unrelated donors ≥8/10 HLA matched. Hematopoietic cell transplantation-specific comorbidity index scores were intermediate and high for 84%. Conditioning regimens were all myeloablative. Grafts were peripheral blood stem cells (97%) containing CD3 dose ≤10/kg body weight, without pharmacologic GVHD prophylaxis. With median follow-up of 70 months among survivors, Kaplan-Meier estimates of overall and relapse-free survival were 44% and 41%, respectively (4 years). Cumulative incidence of nonrelapse mortality at day +100 was only 10%. Incidence of GVHD for acute (grades II to IV) was 9% at day +100 and for chronic was 7% at 2 and 4 years (8 extensive, 1 overlap). Median Karnofsky performance status for patients > 2 years post-transplant was 90%. As 1 of the largest reports for patients ≥2 aged ≥55 years receiving TCD HSCTs, it demonstrates curative therapy with minimal GVHD, similar to that observed in a younger population.

摘要

T 细胞耗竭(TCD)异基因造血干细胞移植(HSCT)是成人血液系统恶性肿瘤的治愈性治疗方法,可降低移植物抗宿主病(GVHD)而不增加复发率。我们回顾性分析了一家中心 11 年的 214 例年龄≥55 岁患者的单中心经验,以确定老年患者的耐受性和疗效。大多数患者(70%)患有髓系疾病,大多数急性白血病处于缓解期。中位年龄为 61 岁,相关和无关供者≥8/10 HLA 匹配。84%的患者造血细胞移植特异性合并症指数评分处于中高度。预处理方案均为清髓性。移植物为外周血干细胞(97%),含 CD3 剂量≤10/kg 体重,无药物预防 GVHD。在幸存者中,中位随访 70 个月,总生存和无复发生存的 Kaplan-Meier 估计分别为 44%和 41%(4 年)。存活患者+100 天非复发死亡率的累积发生率仅为 10%。急性(II 至 IV 级)GVHD 的发生率为+100 天时为 9%,慢性 GVHD 的发生率为 2 年和 4 年时为 7%(8 例广泛型,1 例重叠型)。移植后>2 年患者的中位 Karnofsky 体能状态为 90%。作为接受 TCD HSCT 的年龄≥55 岁≥2 岁患者的最大报告之一,它证明了具有最小 GVHD 的治愈性治疗,与年轻人群观察到的相似。

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