门诊外周血造血细胞移植后的移植物抗宿主病:拉美医学协会单中心经验。

IF 2.3 4区 医学 Q2 HEMATOLOGY Expert Review of Hematology Pub Date : 2024-01-01 Epub Date: 2024-01-17 DOI:10.1080/17474086.2024.2305372
José Carlos Jaime-Pérez, Jesús Daniel Meléndez-Flores, Jorge Valdespino-Valdes, Andrés Gómez-De León, Perla Rocío Colunga-Pedraza, César Homero Gutiérrez-Aguirre, Olga Graciela Cantú-Rodríguez, David Gómez-Almaguer
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引用次数: 0

摘要

背景:HLA相容性可预测异基因造血细胞移植(allo-HCT)和移植物抗宿主疾病(GvHD)的结果。关于采用减低强度调理(RIC)的门诊 HLA 相同和单倍体-HCT 的 GvHD 结果,目前还没有足够的信息:研究设计:我们比较了不同类型供体的GvHD结果,并报告了196名成人中与GvHD相关的风险因素。干细胞来源为T细胞完整的外周血。对于单倍体受者(107 例),预防性抗宿主疾病的方法是移植后环磷酰胺 (PT-CY)、霉酚酸和降钙素抑制剂;对于 HLA 相同受者(89 例),预防性抗宿主疾病的方法是口服环孢素 (CsA) 加甲氨蝶呤静脉注射:196例HCT移植患者的aGvHD和cGvHD发生率在不同HCT类型中相似。aGvHD严重程度相当,但单倍体组中严重cGvHD发生率较低(p = .011)。单倍体和 HLA 相同受者的百日累积 aGvHD 发生率 (CI) 分别为 31% 和 33% (p = .84);两年的 cGvHD CI 分别为 32% 和 38% (p = .6)。单倍体受者的类固醇难治性 cGvHD 较少(p = .043)。有cGvHD的患者2年复发率较低(p = .003);aGvHD和cGvHD分别带来较高的OS(p = .010和p = .001)。男性对类固醇难治性 cGvHD 有保护作用(p = .028):结论:HLA相同和单倍体移植组的急性和慢性GvHD发生率相当。
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Graft-versus-host disease after an outpatient peripheral blood hematopoietic cell transplant using reduced-intensity conditioning: a single-center LATAM experience.

Background: HLA compatibility predicts allogeneic hematopoietic cell transplant (allo-HCT) and graft-versus-host disease (GvHD) outcomes. There is insufficient information regarding GvHD outcomes for outpatient HLA-identical and haploidentical-HCT employing reduced-intensity conditioning (RIC).

Research design and methods: We compare GvHD outcomes between donor types and report risk factors associated with GvHD. Stem cell source was T-cell replete peripheral blood. GvHD prophylaxis was post-transplant cyclophosphamide (PT-CY), mycophenolic acid, and calcineurin inhibitors for haploidentical (n = 107) and oral cyclosporine (CsA) plus methotrexate i.v. for HLA-identical (n = 89) recipients.

Results: One hundred and ninety-six HCT transplant patients were included. aGvHD and cGvHD frequency were similar between HCT types. aGvHD severity was comparable, but severe cGvHD was less frequent in the haploidentical group (p = .011). One-hundred-day cumulative incidence (CI) of aGvHD for haploidentical and HLA-identical was 31% and 33% (p = .84); 2-year CI of cGvHD was 32% and 38% (p = .6), respectively. Haploidentical recipients had less steroid-refractory cGvHD (p = .043). Patients with cGvHD had less 2-year relapse (p = .003); both aGvHD and cGvHD conferred higher OS (p = .010 and p = .001), respectively. Male sex was protective for steroid-refractory cGvHD (p = .028).

Conclusions: Acute and chronic GvHD rates were comparable between HLA-identical and haploidentical transplant groups. cGvHD severity was lower in the haploidentical group.

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来源期刊
CiteScore
4.70
自引率
3.60%
发文量
98
审稿时长
6-12 weeks
期刊介绍: Advanced molecular research techniques have transformed hematology in recent years. With improved understanding of hematologic diseases, we now have the opportunity to research and evaluate new biological therapies, new drugs and drug combinations, new treatment schedules and novel approaches including stem cell transplantation. We can also expect proteomics, molecular genetics and biomarker research to facilitate new diagnostic approaches and the identification of appropriate therapies. Further advances in our knowledge regarding the formation and function of blood cells and blood-forming tissues should ensue, and it will be a major challenge for hematologists to adopt these new paradigms and develop integrated strategies to define the best possible patient care. Expert Review of Hematology (1747-4086) puts these advances in context and explores how they will translate directly into clinical practice.
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