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2
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Combining the Disease Risk Index and Hematopoietic Cell Transplant Co-Morbidity Index provides a comprehensive prognostic model for CD34-selected allogeneic transplantation.将疾病风险指数与造血细胞移植共病指数相结合,可为CD34选择的异基因移植提供一个全面的预后模型。
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本文引用的文献

1
A Chemotherapy-Only Regimen of Busulfan, Melphalan, and Fludarabine, and Rabbit Antithymocyte Globulin Followed by Allogeneic T-Cell Depleted Hematopoietic Stem Cell Transplantations for the Treatment of Myeloid Malignancies.仅用化疗药物白消安、马法兰和氟达拉滨,以及兔抗胸腺细胞球蛋白,随后进行异基因 T 细胞耗竭的造血干细胞移植治疗髓系恶性肿瘤。
Biol Blood Marrow Transplant. 2017 Dec;23(12):2088-2095. doi: 10.1016/j.bbmt.2017.07.004. Epub 2017 Jul 12.
2
Sixty as the new forty: considerations on older related stem cell donors.六十当作新四十:关于老年相关干细胞供体的思考
Bone Marrow Transplant. 2017 Jan;52(1):15-19. doi: 10.1038/bmt.2016.201. Epub 2016 Aug 8.
3
TCR-alpha/beta and CD19 depletion and treosulfan-based conditioning regimen in unrelated and haploidentical transplantation in children with acute myeloid leukemia.TCR-α/β和CD19清除以及基于曲奥舒凡的预处理方案用于儿童急性髓系白血病非亲缘及单倍体移植
Bone Marrow Transplant. 2016 May;51(5):668-74. doi: 10.1038/bmt.2015.343. Epub 2016 Jan 25.
4
Is there a role for therapy after transplant?移植后进行治疗是否有作用?
Best Pract Res Clin Haematol. 2015 Jun-Sep;28(2-3):124-32. doi: 10.1016/j.beha.2015.10.009. Epub 2015 Oct 22.
5
Phase II Study of Allogeneic Transplantation for Older Patients With Acute Myeloid Leukemia in First Complete Remission Using a Reduced-Intensity Conditioning Regimen: Results From Cancer and Leukemia Group B 100103 (Alliance for Clinical Trials in Oncology)/Blood and Marrow Transplant Clinical Trial Network 0502.采用减低剂量预处理方案对首次完全缓解的老年急性髓系白血病患者进行异基因移植的II期研究:癌症与白血病B组100103(肿瘤临床试验联盟)/血液与骨髓移植临床试验网络0502的结果
J Clin Oncol. 2015 Dec 10;33(35):4167-75. doi: 10.1200/JCO.2015.62.7273. Epub 2015 Nov 2.
6
CD34-Selected Hematopoietic Stem Cell Transplants Conditioned with Myeloablative Regimens and Antithymocyte Globulin for Advanced Myelodysplastic Syndrome: Limited Graft-versus-Host Disease without Increased Relapse.采用清髓方案和抗胸腺细胞球蛋白预处理的CD34选择的造血干细胞移植治疗晚期骨髓增生异常综合征:移植物抗宿主病有限且复发率未增加。
Biol Blood Marrow Transplant. 2015 Dec;21(12):2106-2114. doi: 10.1016/j.bbmt.2015.07.010. Epub 2015 Jul 14.
7
Improved immune recovery after transplantation of TCRαβ/CD19-depleted allografts from haploidentical donors in pediatric patients.儿科患者接受来自单倍体相合供体的TCRαβ/CD19去除的同种异体移植物移植后免疫恢复得到改善。
Bone Marrow Transplant. 2015 Jun;50 Suppl 2:S6-10. doi: 10.1038/bmt.2015.87.
8
Comparison of outcomes at two institutions of patients with ALL receiving ex vivo T-cell-depleted or unmodified allografts.两家机构中接受体外T细胞去除或未修饰同种异体移植物的急性淋巴细胞白血病患者的结局比较。
Bone Marrow Transplant. 2015 Apr;50(4):493-8. doi: 10.1038/bmt.2014.302. Epub 2015 Jan 26.
9
Early lymphocyte recovery at 28 d post-transplant is predictive of reduced risk of relapse in patients with acute myeloid leukemia transplanted with peripheral blood stem cell grafts.移植后28天早期淋巴细胞恢复可预测接受外周血干细胞移植的急性髓系白血病患者复发风险降低。
Eur J Haematol. 2014 Oct;93(4):273-80. doi: 10.1111/ejh.12338. Epub 2014 Apr 29.
10
Depletion of T-cell receptor alpha/beta and CD19 positive cells from apheresis products with the CliniMACS device.用 CliniMACS 设备从单采产品中去除 T 细胞受体 α/β 和 CD19 阳性细胞。
Cytotherapy. 2013 Oct;15(10):1253-8. doi: 10.1016/j.jcyt.2013.05.014.

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.

DOI:10.1016/j.bbmt.2017.06.024
PMID:28734876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10715069/
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。