Department of Hematology, Oncology, Clinical Immunology and Rheumatology, Center for Internal Medicine, University Hospital Tuebingen, Tuebingen, Germany.
University Children's Hospital Wuerzburg, Wuerzburg, Germany.
Bone Marrow Transplant. 2022 Mar;57(3):423-430. doi: 10.1038/s41409-021-01551-z. Epub 2021 Dec 24.
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.
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。