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间充质基质细胞治疗儿童造血细胞移植相关并发症(移植物抗宿主病、出血性膀胱炎、移植物失败和移植物功能不良):单中心经验

Mesenchymal stromal cells in the treatment of pediatric hematopoietic cell transplantation-related complications (graft vs. host disease, hemorrhagic cystitis, graft failure and poor graft function): a single center experience.

作者信息

Pérez-Torres Lobato Maria, Benitez-Carabante Maria Isabel, Alonso Laura, Torrents Silvia, Castillo Flores Nerea, Uria Oficialdegui Maria Luz, Panesso Melissa, Alonso-Martínez Carla, Oliveras Maria, Renedo-Miró Berta, Vives Joaquim, Diaz-de-Heredia Cristina

机构信息

Department of Paediatric Oncology and Haematology, Vall D'Hebron University Hospital, Barcelona, Spain.

Vall D'Hebron Research Institute (VHIR), Barcelona, Spain.

出版信息

Front Pediatr. 2024 May 9;12:1375493. doi: 10.3389/fped.2024.1375493. eCollection 2024.

Abstract

OBJECTIVES

To describe mesenchymal stromal cells (MSCs) in the treatment of hematopoietic stem cell transplantation (HSCT) complications and to assess its safety and efficacy.

METHODS

Single-center retrospective study (2016-2023). Patients under 20 years who received MSCs for the treatment of HSCT-related complications were included.

RESULTS

Thirty patients (53.7% boys), median age at transplant 11 years (range 2-19) were included. MSCs indications were: graft-vs.-host disease (GVHD) in 18 patients (60%), of them 13 had acute GVHD (43.3%) and 5 chronic GVHD (16.7%); Grade 3-4 hemorrhagic cystitis (HC) in 4 (13.3%); poor graft function (PGF) in 6 (20%), 5 of them receiving MSCs with a CD34 stem cell-boost coinfusion; graft failure (GF) in 2 (6.7%), to enhance engraftment after a subsequent HSCT. Infusion-related-adverse-events were not reported. Overall response (OR) was 83% (25/30); 44% of responders (11/25) showed complete response (CR). OR for GVHD, HC, PGF and GF was 83.3%, 100%, 66.7% and 100% respectively. Response rate was 40% (95% CI: 20-55) and 79% (95% CI: 57-89) at 15 and 30 days. With a median follow-up of 21 months (IQR11-52.5), overall survival (OS) was 86% (95% CI: 74-100) and 79% (95% CI: 65-95) at 6 and 12 months post-MSCs infusion.

CONCLUSION

In our study, the most frequent indication of MSCs was refractory aGVHD (43.3%). Response rates were high (OR 83%) and safety profile was good.

摘要

目的

描述间充质基质细胞(MSCs)在治疗造血干细胞移植(HSCT)并发症中的应用,并评估其安全性和有效性。

方法

单中心回顾性研究(2016 - 2023年)。纳入20岁以下接受MSCs治疗HSCT相关并发症的患者。

结果

共纳入30例患者(53.7%为男孩),移植时中位年龄11岁(范围2 - 19岁)。MSCs的应用指征为:18例(60%)移植物抗宿主病(GVHD),其中13例为急性GVHD(43.3%),5例为慢性GVHD(16.7%);4例(13.3%)为3 - 4级出血性膀胱炎(HC);6例(20%)为移植物功能不良(PGF),其中5例在输注MSCs时联合输注CD34干细胞以增强效果;2例(6.7%)为移植失败(GF),在后续HSCT后输注以促进植入。未报告与输注相关的不良事件。总体缓解率(OR)为83%(25/30);44%的缓解者(11/25)显示完全缓解(CR)。GVHD、HC、PGF和GF的OR分别为83.3%、100%、66.7%和100%。在15天和30天时缓解率分别为40%(95%CI:20 - 55)和79%(95%CI:57 - 89)。中位随访21个月(IQR11 - 52.5),在输注MSCs后6个月和12个月时总生存率(OS)分别为86%(95%CI:74 - 100)和79%(95%CI:65 - 95)。

结论

在我们的研究中,MSCs最常见的应用指征为难治性急性GVHD(43.3%)。缓解率高(OR 83%)且安全性良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/409b/11112085/fb4e9b612a62/fped-12-1375493-g001.jpg

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