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一项多中心 I/II 期临床试验的结果:TCRαβ 和 CD19 耗竭的单倍体相合造血干细胞移植治疗成人和儿童患者。

Results of a multicenter phase I/II trial of TCRαβ and CD19-depleted haploidentical hematopoietic stem cell transplantation for adult and pediatric patients.

机构信息

Department of Hematology, Oncology, Clinical Immunology and Rheumatology, Center for Internal Medicine, University Hospital Tuebingen, Tuebingen, Germany.

University Children's Hospital Wuerzburg, Wuerzburg, Germany.

出版信息

Bone Marrow Transplant. 2022 Mar;57(3):423-430. doi: 10.1038/s41409-021-01551-z. Epub 2021 Dec 24.

DOI:10.1038/s41409-021-01551-z
PMID:34952929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8702395/
Abstract

Hematopoietic stem cell transplantation (HSCT) from haploidentical donors is a viable option for patients lacking HLA-matched donors. Here we report the results of a prospective multicenter phase I/II trial of transplantation of TCRαβ and CD19-depleted peripheral blood stem cells from haploidentical family donors after a reduced-intensity conditioning with fludarabine, thiotepa, and melphalan. Thirty pediatric and 30 adult patients with acute leukemia (n = 43), myelodysplastic or myeloproliferative syndrome (n = 6), multiple myeloma (n = 1), solid tumors (n = 6), and non-malignant disorders (n = 4) were enrolled. TCR αβ/CD19-depleted grafts prepared decentrally at six manufacturing sites contained a median of 12.1 × 10 CD34 cells/kg and 14.2 × 10 TCRαβ T-cells/kg. None of the patients developed grade lll/IV acute graft-versus-host disease (GVHD) and only six patients (10%) had grade II acute GVHD. With a median follow-up of 733 days 36/60 patients are alive. The cumulative incidence of non-relapse mortality at day 100, 1 and 2 years after HSCT was 5%, 15%, and 17% for all patients, respectively. Estimated probabilities of overall and disease-free survival at 2 years were 63% and 50%, respectively. Based on these promising results in a high-risk patient cohort, haploidentical HSCT using TCRαβ/CD19-depleted grafts represents a viable treatment option.

摘要

造血干细胞移植(HSCT)来自单倍体供体是缺乏 HLA 匹配供体的患者的可行选择。在这里,我们报告了一项前瞻性多中心 I/II 期试验的结果,该试验使用经过氟达拉滨、噻替哌和马法兰预处理的单倍体家族供体 TCRαβ 和 CD19 耗尽的外周血干细胞进行移植。共有 30 名儿科和 30 名成人急性白血病患者(n=43)、骨髓增生异常或骨髓增生性综合征患者(n=6)、多发性骨髓瘤患者(n=1)、实体瘤患者(n=6)和非恶性疾病患者(n=4)入组。在六个制造地点分散制备的 TCRαβ/CD19 耗尽移植物中位数包含 12.1×10 CD34 细胞/kg 和 14.2×10 TCRαβ T 细胞/kg。没有患者发生 III/IV 级急性移植物抗宿主病(GVHD),只有 6 名患者(10%)发生 II 级急性 GVHD。在中位随访 733 天后,60 名患者中有 36 名存活。所有患者在 HSCT 后 100 天、1 年和 2 年的非复发死亡率的累积发生率分别为 5%、15%和 17%。2 年时的总生存率和无病生存率估计分别为 63%和 50%。基于高危患者队列中的这些有希望的结果,使用 TCRαβ/CD19 耗尽移植物的单倍体 HSCT 是一种可行的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ae3/8907062/05b44ffa6435/41409_2021_1551_Fig6_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ae3/8907062/65600d2d81ab/41409_2021_1551_Fig2_HTML.jpg
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