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与单倍体造血干细胞移植后单独使用移植后环磷酰胺相比,移植后环磷酰胺联合抗胸腺细胞球蛋白可降低血清白细胞介素-6水平。

Post-transplant cyclophosphamide plus anti-thymocyte globulin decreased serum IL-6 levels when compared with post-transplant cyclophosphamide alone after haploidentical hematopoietic stem cell transplantation.

作者信息

Koh Jeong Suk, Lee Myung-Won, Pham Thi Thuy Duong, Heo Bu Yeon, Choi Suyoung, Lee Sang-Woo, Seo Wonhyoung, Kang Sora, Lee Seul Bi, Kim Chul Hee, Ryu Hyewon, Eun Hyuk Soo, Lee Hyo-Jin, Yun Hwan-Jung, Jo Deog-Yeon, Song Ik-Chan

机构信息

Division of Hematology and Oncology, Department of Internal Medicine, Chungnam National University Hospital, 282 Munwha-Ro, Jung-Gu, Daejeon, 35015, South Korea.

Department of Medical Science, Daejeon, South Korea.

出版信息

Blood Res. 2025 Jan 15;60(1):5. doi: 10.1007/s44313-024-00049-z.

DOI:10.1007/s44313-024-00049-z
PMID:39812969
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11735700/
Abstract

BACKGROUND

Post-transplantation cyclophosphamide (PTCy) and anti-thymocyte globulin (ATG) are common prophylactic strategies for graft-versus-host disease (GVHD) after haploidentical hematopoietic stem cell transplantation (haplo-HSCT). Interleukin (IL)-6 is a surrogate marker for cytokine release syndrome (CRS) and acute GVHD.

METHOD

The clinical outcomes and complications of haplo-HSCT with PTCy plus ATG versus PTCy monotherapy were compared according to serum IL-6 levels at Chungnam National University Hospital (Daejeon, South Korea) from January 2019 to February 2023.

RESULTS

Forty patients who underwent haplo-HSCT were analyzed. A significant difference in IL-6 levels was observed between the PTCy plus ATG and PTCy alone groups (7.47 ± 10.55 vs. 117.65 ± 127.67; p = 0.003). More patients in the PTCy plus ATG group had a CRS grade of 0 than in the PTCy alone group (p < 0.001). Serum IL-6 levels were associated with grades II-IV acute GVHD (r = 0.547, p < 0.001). The cumulative incidence (CI) of grades II-IV acute GVHD was significantly higher in the PTCy alone group (67.9% vs. 4.8%; p < 0.001). No significant difference in the CI for chronic GVHD was detected between the PTCy plus ATG and PTCy alone groups (72.1% vs. 82.0%; p = 0.730). The CI of 1-year non-relapse mortality was significantly higher in the PTCy alone group than in the PTCy plus ATG group (42.2% vs. 15.9%; p = 0.022). The 1-year overall survival (OS) was significantly better in the PTCy plus ATG group (75.9% vs. 35.3%; p = 0.011). The 1-year GVHD-free, relapse-free survival rate was 29.4% in the PTCy alone group and 54.0% in the PTCy plus ATG group (p = 0.038).

CONCLUSION

Serum IL-6 levels were higher in the PTCy alone group than in the PTCy plus ATG group. The addition of ATG before stem cell infusion affected IL-6 levels and reduced the incidences of CRS and grade II-IV acute GVHD in haplo-HSCT patients. This study suggests that PTCy plus ATG as GVHD prophylaxis in haplo-HSCT is beneficial in terms of clinical outcomes and complications of HSCT.

摘要

背景

移植后环磷酰胺(PTCy)和抗胸腺细胞球蛋白(ATG)是单倍体相合造血干细胞移植(haplo-HSCT)后预防移植物抗宿主病(GVHD)的常用策略。白细胞介素(IL)-6是细胞因子释放综合征(CRS)和急性GVHD的替代标志物。

方法

2019年1月至2023年2月,在韩国忠南国立大学医院,根据血清IL-6水平,比较了PTCy联合ATG与PTCy单药治疗haplo-HSCT的临床结局和并发症。

结果

分析了40例行haplo-HSCT的患者。PTCy联合ATG组与PTCy单药组的IL-6水平存在显著差异(7.47±10.55 vs. 117.65±127.67;p=0.003)。PTCy联合ATG组CRS 0级的患者比PTCy单药组更多(p<0.001)。血清IL-6水平与II-IV级急性GVHD相关(r=0.547,p<0.001)。PTCy单药组II-IV级急性GVHD的累积发生率显著更高(67.9% vs. 4.8%;p<0.001)。PTCy联合ATG组与PTCy单药组慢性GVHD的累积发生率无显著差异(72.1% vs. 82.0%;p=0.730)。PTCy单药组1年非复发死亡率的累积发生率显著高于PTCy联合ATG组(42.2% vs. 15.9%;p=0.022)。PTCy联合ATG组1年总生存率显著更好(75.9% vs. 35.3%;p=0.011)。PTCy单药组1年无GVHD、无复发生存率为29.4%,PTCy联合ATG组为54.0%(p=0.038)。

结论

PTCy单药组的血清IL-6水平高于PTCy联合ATG组。在干细胞输注前加用ATG可影响IL-6水平,并降低haplo-HSCT患者CRS和II-IV级急性GVHD的发生率。本研究表明,PTCy联合ATG作为haplo-HSCT中GVHD的预防措施,在HSCT的临床结局和并发症方面是有益的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f566/11735700/ed6428a4260f/44313_2024_49_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f566/11735700/ec188f9354c0/44313_2024_49_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f566/11735700/fdbdd2f92b9b/44313_2024_49_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f566/11735700/ed6428a4260f/44313_2024_49_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f566/11735700/ec188f9354c0/44313_2024_49_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f566/11735700/fdbdd2f92b9b/44313_2024_49_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f566/11735700/ed6428a4260f/44313_2024_49_Fig3_HTML.jpg

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