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单单位脐带血与间充质基质细胞骨内联合移植并采用减低剂量预处理方案的I期研究

Phase I study of intra-osseous co-transplantation of a single-unit cord blood and mesenchymal stromal cells with reduced intensity conditioning regimens.

作者信息

Wang Jiasheng, Sanati Farhad, Firoozmand Amin, Fu Pingfu, Kolk Merle, Reese-Koc Jane, de Lima Marcos, Boughan Kirsten, Cooper Brenda, Caimi Paolo, Gallogly Molly, Otegbeye Folashade, Tomlinson Benjamin, Metheny Leland

机构信息

Department of Hematology/Oncology, University Hospitals Seidman Cancer Center, Cleveland, OH, United States.

Case Western Reserve University, Cleveland, OH, United States.

出版信息

Front Oncol. 2023 May 3;13:1186532. doi: 10.3389/fonc.2023.1186532. eCollection 2023.

DOI:10.3389/fonc.2023.1186532
PMID:37207167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10191226/
Abstract

Cord blood (CB) is a valuable graft source for patients undergoing allogeneic hematopoietic cell transplant (HCT) who lack human leukocyte antigen (HLA)-matched donors. However, single-unit CB-HCT is limited by the insufficient cell dose and slow engraftment. To overcome these limitations, we combined a single-unit CB with third-party healthy donors' bone marrow (BM) derived mesenchymal stromal cells (MSCs) to improve engraftment and injected intra-osseously (IO) to enhance homing. In this phase I clinical trial, six patients with high-risk hematologic malignancies were enrolled and received allogeneic HCT using reduced intensity conditioning regimens. The primary objective was to determine the engraftment rate at day 42. The median age of enrolled patients was 68 years, and only one patient was in complete remission at the time of HCT. The median CB total nucleated cell dose was 3.2x10/kg. No serious adverse events were reported. Two patients had early deaths due to persistent disease and multi-drug resistant bacterial infection, respectively. Of the remaining four evaluable patients, all had successful neutrophil engraftment in a median of 17.5 days. No grade 3 or higher acute graft-versus-host disease (GvHD) was observed, and only one patient developed moderate-extensive chronic GvHD. In conclusion, IO co-transplantation of a single-unit CB and MSCs was feasible and resulted in a reasonable engraftment rate in these very high-risk patients.

摘要

脐带血(CB)是缺乏人类白细胞抗原(HLA)匹配供体的异基因造血细胞移植(HCT)患者的宝贵移植物来源。然而,单单位脐带血造血细胞移植受到细胞剂量不足和植入缓慢的限制。为了克服这些限制,我们将单单位脐带血与第三方健康供体的骨髓(BM)来源的间充质基质细胞(MSCs)联合使用以改善植入,并通过骨内(IO)注射以增强归巢。在这项I期临床试验中,招募了6例高危血液系统恶性肿瘤患者,并采用减低强度预处理方案接受异基因造血细胞移植。主要目的是确定第42天的植入率。入组患者的中位年龄为68岁,造血细胞移植时只有1例患者处于完全缓解状态。脐带血总核细胞剂量中位数为3.2×10/kg。未报告严重不良事件。2例患者分别因持续性疾病和多重耐药细菌感染早期死亡。在其余4例可评估患者中,所有患者均在中位17.5天成功实现中性粒细胞植入。未观察到3级或更高的急性移植物抗宿主病(GvHD),只有1例患者发生中度广泛的慢性移植物抗宿主病。总之,单单位脐带血和间充质基质细胞的骨内联合移植是可行的,并且在这些极高危患者中产生了合理的植入率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef50/10191226/30c12064f271/fonc-13-1186532-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef50/10191226/e283644f3881/fonc-13-1186532-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef50/10191226/30c12064f271/fonc-13-1186532-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef50/10191226/e283644f3881/fonc-13-1186532-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef50/10191226/30c12064f271/fonc-13-1186532-g002.jpg

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