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造血干细胞移植治疗非间变大细胞外周 T 细胞淋巴瘤的儿科患者:一项 EBMT 儿科疾病工作组研究。

Hematopoietic stem cell transplantation for pediatric patients with non-anaplastic peripheral T-cell lymphoma. An EBMT pediatric diseases working party study.

机构信息

University Hospital RWTH Aachen, Department of Pediatric Hematology, Oncology, and Stem Cell Transplantation, Aachen, Germany.

EBMT Paris Office, Hôpital Saint Antoine, Paris, France.

出版信息

Bone Marrow Transplant. 2024 May;59(5):604-614. doi: 10.1038/s41409-024-02226-1. Epub 2024 Feb 8.

Abstract

Peripheral T-cell lymphomas (PTCL) other than anaplastic large-cell lymphoma are rare in children, and the role of hematopoietic stem cell transplantation (HSCT) has not been clarified yet. In a retrospective analysis of registry-data of the European Society for Blood and Marrow Transplantation we analyzed 55 patients aged < 18 years who received allogeneic (N = 46) or autologous (N = 9) HSCT for PTCL. Median age at HSCT was 13.9 years; 33 patients (60%) were in first remission, and 6 (19%) in progression at HSCT. Conditioning was myeloablative in 87% of the allogeneic HSCTs and in 27 (58.7%) based on total body irradiation. After allogeneic HSCT the 5-year overall- and progression-free survival was 58.9% (95% CI 42.7-71.9) and 52.6% (95% CI 36.8-66.1), respectively. 5-year relapse incidence was 27.6% (95% CI 15.1-41.6), the non-relapse mortality rate was 19.8% (95% CI 9.7-32.6). Five of the six patients with progression at HSCT died. Seven of nine patients after autologous HSCT were alive and disease-free at last follow-up. Our data suggest a role of allogeneic HSCT in consolidation-treatment of patients with high-risk disease, who reach at least partial remission after primary- or relapse-therapy, whereas patients with therapy-refractory or progressive disease prior to transplantation do not profit from HSCT.

摘要

外周 T 细胞淋巴瘤(PTCL)除间变大细胞淋巴瘤外,在儿童中较为罕见,其造血干细胞移植(HSCT)的作用尚未明确。我们对欧洲血液和骨髓移植学会注册数据进行了回顾性分析,纳入了 55 名接受异基因(N=46)或自体(N=9)HSCT 治疗的 PTCL <18 岁的患者。HSCT 时的中位年龄为 13.9 岁;33 名患者(60%)处于首次缓解期,6 名(19%)在 HSCT 时处于进展期。87%的异基因 HSCT 采用清髓性预处理,27 例(58.7%)基于全身照射。异基因 HSCT 后 5 年总生存率和无进展生存率分别为 58.9%(95%CI 42.7-71.9)和 52.6%(95%CI 36.8-66.1)。5 年复发率为 27.6%(95%CI 15.1-41.6),非复发死亡率为 19.8%(95%CI 9.7-32.6)。6 名进展期患者中有 5 名死亡。9 名接受自体 HSCT 患者中有 7 名在最后一次随访时存活且无疾病。我们的数据表明,异基因 HSCT 可用于巩固治疗高危疾病患者,这些患者在初次或复发治疗后至少达到部分缓解,而移植前对治疗有抵抗或进展的患者不能从 HSCT 中获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/939a/11073963/a9f0d6724c7f/41409_2024_2226_Fig1_HTML.jpg

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