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间充质基质细胞治疗改善造血干细胞移植后肺炎患儿的预后:一项回顾性队列研究。

Mesenchymal stromal cell treatment improves outcomes in children with pneumonia post-hematopoietic stem cell transplantation: a retrospective cohort study.

机构信息

Department of Hematology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, 510623, Guangdong, China.

出版信息

Stem Cell Res Ther. 2022 Jun 28;13(1):277. doi: 10.1186/s13287-022-02960-7.

DOI:10.1186/s13287-022-02960-7
PMID:35765041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9241242/
Abstract

BACKGROUND

Hematopoietic stem cell transplantation (HSCT) is a standard therapy strategy for most malignant disorders in children. However, transplant-related pneumonia remains a major therapy challenge and mesenchymal stromal cells (MSCs) are rarely reported in HSCT-related pneumonia. The aim of our study was to assess the efficacy of MSC for HSCT-related pneumonia in children.

METHODS

We retrospectively retrieved HSCT-related (severe and non-severe) pneumonia cases (aged < 18 years), which underwent MSC treatment (MSC group) or non-MSC treatment (non-MSC group) in Guangzhou Women and Children's Medical Center, from December 2017 to December 2019. We investigated outcomes of the two different treatments among severe cases and non-severe cases, respectively. The primary endpoints were differences in overall cure rate and time to cure between MSC and non-MSC groups. The secondary endpoints were 180-day overall survival and cumulative cure rate.

RESULTS

Finally, 31 severe pneumonia cases (16 in MSC group, 15 in non-MSC group) and 76 non-severe cases (31 in MSC group, 45 in non-MSC group) were enrolled in this study. Among severe pneumonia cases, overall cure rate in MSC group was significant higher than that in non-MSC group (12[75.0%] vs. 5[33.3%]; OR = 6.00, 95% CI [1.26-28.5]; p = 0.020); the time (days) to cure in MSC group was dramatically reduced compared with that in non-MSC group (36 [19-52] vs. 62 [42-81]; OR = 0.32, 95% CI [0.12-0.88]; p = 0.009); the 180-day overall survival in MSC group was better than that in non-MSC group (74.5% [45.4-89.6] vs. 33.3% [12.2-56.4]; p = 0.013). Among non-severe pneumonia cases, the time (days) to cure in MSC group was notably decreased compared with that in non-MSC group (28 [24-31] vs. 33 [26-39]; OR = 0.31, 95% CI [0.18-0.56]; p = 0.003). Compared with non-MSC group, MSC-treated patients achieved significant improvements of cumulative cure rate not only in severe pneumonia cases (p = 0.027), but also in non-severe cases (p < 0.001).

CONCLUSIONS

This study revealed that MSC treatment could contribute to improving outcomes in children with pneumonia post-HSCT, especially in severe cases. These findings suggest MSC treatment as a promising therapy for HSCT-related pneumonia in children.

摘要

背景

造血干细胞移植(HSCT)是儿童大多数恶性疾病的标准治疗策略。然而,与移植相关的肺炎仍然是一个主要的治疗挑战,间充质基质细胞(MSCs)在 HSCT 相关肺炎中很少报道。我们的研究目的是评估 MSCs 治疗儿童 HSCT 相关肺炎的疗效。

方法

我们回顾性地检索了 2017 年 12 月至 2019 年在广州妇女儿童医疗中心接受 MSC 治疗(MSC 组)或非 MSC 治疗(非 MSC 组)的 HSCT 相关(严重和非严重)肺炎病例(年龄<18 岁)。我们分别研究了两组中严重病例和非严重病例的治疗结果。主要终点是 MSC 组和非 MSC 组之间总治愈率和治愈时间的差异。次要终点是 180 天总生存率和累积治愈率。

结果

最终,本研究纳入了 31 例严重肺炎病例(MSC 组 16 例,非 MSC 组 15 例)和 76 例非严重肺炎病例(MSC 组 31 例,非 MSC 组 45 例)。在严重肺炎病例中,MSC 组的总治愈率显著高于非 MSC 组(12[75.0%]vs.5[33.3%];OR=6.00,95%CI[1.26-28.5];p=0.020);MSC 组的治愈时间(天)明显短于非 MSC 组(36[19-52]vs.62[42-81];OR=0.32,95%CI[0.12-0.88];p=0.009);MSC 组 180 天总生存率优于非 MSC 组(74.5%[45.4-89.6]vs.33.3%[12.2-56.4];p=0.013)。在非严重肺炎病例中,MSC 组的治愈时间(天)明显短于非 MSC 组(28[24-31]vs.33[26-39];OR=0.31,95%CI[0.18-0.56];p=0.003)。与非 MSC 组相比,MSC 治疗组不仅在严重肺炎病例(p=0.027),而且在非严重肺炎病例(p<0.001)中累积治愈率均有显著提高。

结论

本研究表明,MSC 治疗可改善 HSCT 后儿童肺炎的预后,特别是在严重病例中。这些发现表明 MSC 治疗是儿童 HSCT 相关肺炎有前途的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9494/9241242/bddcf5146731/13287_2022_2960_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9494/9241242/23c4fb204fbd/13287_2022_2960_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9494/9241242/bddcf5146731/13287_2022_2960_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9494/9241242/23c4fb204fbd/13287_2022_2960_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9494/9241242/bddcf5146731/13287_2022_2960_Fig2_HTML.jpg

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