癌症儿童亲属造血干细胞移植后的“移植物-血管-宿主”病、预防方案及与“移植物-Versus-肿瘤”效应的相关性:回顾性队列研究

Q3 Medicine Onkopediatria Pub Date : 2019-07-24 DOI:10.15690/onco.v6i2.2023
N. Subbotina, I. Dolgopolov, Vidmante V. Daylidite, V. K. Boyarshinov, G. Mentkevich
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引用次数: 0

摘要

背景移植物抗宿主病(GVHD)是异基因造血干细胞移植(HSCT)的主要并发症,是非复发性死亡率的主要原因。替代供体HSCT的实际问题是GVHD的预防及其与“移植物对抗肿瘤”(GVT)效应的区别。客观的评估非T缺失的单倍造血干细胞移植后极高危癌症儿童GVHD的发病率和严重程度;通过比较环孢菌素(CSA)和他克莫司预防的慢性移植物抗宿主病(chGVHD)与HSCT后GVT效果之间的相关性。方法。我们在回顾性队列研究中提供了自2001年至2018年74例来自亲属的单倍造血干细胞受体的GVHD评估。在23例急性髓系白血病(AML)患者和15例实体瘤患者中评估了chGVHD对HSCT结果的影响。我们分析了接受CSA或他克莫司预防的患者中严重急性和慢性移植物抗宿主病的发生率。后果在我们的研究中,严重aGHVD的发生率为15%,chGVHD为12%。将CSA转换为他克莫司导致严重aGVHD从21%减少到9%,并完全消除严重广泛chGVHD。在AML患者中,haplo-HSCT后控制chGVHD可将复发率从48.7%降低到30%,并将总生存率(OS)从46.5%提高到80.8%。我们还没有看到移植物对实体瘤患者有任何临床意义的抗肿瘤作用。结论在我们的研究中,严重移植物抗宿主病的发生率与来自替代供体的HSCT后的世界数据一致,在从CSA转为他克莫司后下降。我们发现AML患者的chGVHD发展得到控制与HSCT结果改善之间存在一些相关性。单倍体移植物在实体瘤中的移植物抗宿主病作用几乎不存在。
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«Graft-Versus-Host» Disease after Haploidentical Hematopoietic Stem Cell Transplantation from Relative Donors in Children with Cancer, Prophylaxis Regimens and Correlation with «Graft-Versus-Tumor» Effect: a Retrospective Cohort Study
Background. «Graft-versus-host» disease (GVHD) is a major complication of allogeneic Hematopoietic Stem Cell Transplantation (HSCT), the main cause of non-relapse mortality. The actual problems of alternative donors HSCTs are GVHD prophylaxis and its distinction from «graft-versus-tumor» (GVT) effect. Objective. Assessment of incidence and severity of GVHD in children with very high-risk cancer after non-T-depleted haplo-HSCT; searching some correlation between controlled chronic GVHD (chGVHD) and GVT effect after HSCT, compare cyclosporine (CSA) and tacrolimus based GVHD prophylaxis. Methods. We provided the GVHD assessment in 74 recipients of haplo-HSCs from relatives since 2001 till 2018 in retrospective cohort study. Effect of chGVHD on the HSCT results was assessed in 23 patients with acute myeloid leukemia (AML) and 15 patients with solid tumors. We analyzed the incidence of severe acute and chronic GVHD in patients who received CSA or tacrolimus-based prophylaxis. Results. The incidence of severe aGHVD in our study was 15%, chGVHD — 12%. Switch CSA to tacrolimus resulted in reduction of severe aGVHD from 21% to 9% and full elimination of severe extensive chGVHD. Controlled chGVHD after haplo-HSCT was associated with relapse reduction from 48.7% to 30% and improvement of overall survival (OS) from 46.5% to 80.8% in patients with AML. We haven’t seen any clinically significant antitumor effect of graft in patients with solid tumors. Conclusion. In our study the incidence of severe GVHD corresponds to world data after HSCTs from alternative donors, it went down after switch from CSA to tacrolimus. We found some correlation between controlled chGVHD development and HSCT results improvement in patients with AML. The GVT effect of haplo-graft in solid tumors is almost absent.
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Onkopediatria
Onkopediatria Medicine-Pediatrics, Perinatology and Child Health
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