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地中海贫血-free 和移植物抗宿主病-free 生存:土耳其地中海贫血重型造血干细胞移植的结果。

Thalassemia-free and graft-versus-host-free survival: outcomes of hematopoietic stem cell transplantation for thalassemia major, Turkish experience.

机构信息

Medicalpark Antalya Hospital, Pediatric Hematology and Stem Cell Transplantation Unit, Antalya, Turkey.

Istinye University School of Medicine Department of Pediatric Hematology and Oncology Unit, Istanbul, Turkey.

出版信息

Bone Marrow Transplant. 2022 May;57(5):760-767. doi: 10.1038/s41409-022-01613-w. Epub 2022 Feb 24.

Abstract

We report the national data on the outcomes of hematopoietic stem cell transplantation (HSCT) for thalassemia major (TM) patients in Turkey on behalf of the Turkish Pediatric Stem Cell Transplantation Group. We retrospectively enrolled 1469 patients with TM who underwent their first HSCT between 1988 and 2020 in 25 pediatric centers in Turkey. The median follow-up duration and transplant ages were 62 months and 7 years, respectively; 113 patients had chronic graft versus host disease (cGVHD) and the cGVHD rate was 8.3% in surviving patients. Upon the last visit, 30 patients still had cGvHD (2.2%). The 5-year overall survival (OS), thalassemia-free survival (TFS) and thalassemia-GVHD-free survival (TGFS) rates were 92.3%, 82.1%, and 80.8%, respectively. cGVHD incidence was significantly lower in the mixed chimerism (MC) group compared to the complete chimerism (CC) group (p < 0.001). In survival analysis, OS, TFS, and TGFS rates were significantly higher for transplants after 2010. TFS and TGFS rates were better for patients under 7 years and at centers that had performed over 100 thalassemia transplants. Transplants from matched unrelated donors had significantly higher TFS rates. We recommend HSCT before 7 years old in thalassemia patients who have a matched donor for improved outcomes.

摘要

我们代表土耳其儿科干细胞移植组报告了土耳其重型地中海贫血(TM)患者造血干细胞移植(HSCT)结果的全国数据。我们回顾性纳入了 1988 年至 2020 年间在土耳其 25 个儿科中心接受首次 HSCT 的 1469 例 TM 患者。中位随访时间和移植年龄分别为 62 个月和 7 年;113 例患者发生慢性移植物抗宿主病(cGVHD),存活患者的 cGVHD 发生率为 8.3%。在最后一次就诊时,仍有 30 例患者存在 cGvHD(2.2%)。5 年总生存率(OS)、无地中海贫血生存率(TFS)和无地中海贫血-移植物抗宿主病生存率(TGFS)分别为 92.3%、82.1%和 80.8%。混合嵌合体(MC)组的 cGVHD 发生率明显低于完全嵌合体(CC)组(p<0.001)。在生存分析中,2010 年后进行的移植 OS、TFS 和 TGFS 率显著提高。对于年龄小于 7 岁且在已完成超过 100 例地中海贫血移植的中心的患者,TFS 和 TGFS 率更好。与匹配无关供体的移植具有更高的 TFS 率。我们建议在有匹配供体的情况下,年龄小于 7 岁的地中海贫血患者应进行 HSCT,以改善预后。

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