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异基因造血干细胞移植治疗儿童急性髓系白血病首次完全缓解:一项荟萃分析。

Allogeneic hematopoietic stem cell transplantation for pediatric acute myeloid leukemia in first complete remission: a meta-analysis.

机构信息

Pediatric Oncology and Hematology Unit "Lalla Seràgnoli, IRCCS Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy.

Department of Biomedical and Neuromotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.

出版信息

Ann Hematol. 2022 Nov;101(11):2497-2506. doi: 10.1007/s00277-022-04965-x. Epub 2022 Aug 30.

Abstract

Identification of pediatric patients with acute myeloid leukemia (AML) candidates to receive allogeneic hematopoietic stem cell transplantation (allo-HSCT) in first complete remission (CR1) is still a matter of debate. Currently, transplantation is reserved to patients considered at high risk of relapse based on cytogenetics, molecular biology, and minimal residual disease (MRD) assessment. However, no randomized clinical trial exists in the literature comparing transplantation with other types of consolidation therapy. Here, we provide an up-to-date meta-analysis of studies comparing allo-HSCT in CR1 with chemotherapy alone as a post-remission treatment in high-risk pediatric AML. The literature search strategy identified 10 cohorts from 9 studies performing as-treated analysis. The quantitative synthesis showed improved overall survival (OS) (relative risk, 1.15; 95% confidence interval [CI], 1.06-1.24; P = 0.0006) and disease-free survival (relative risk, 1.31; 95% CI, 1.17-1.47; P = 0.0001) in the allo-HSCT group, with increased relapse rate in the chemotherapy group (relative risk, 1.26; 95% CI, 1.07-1.49; P = 0.006). Sensitivity analysis including prospective studies alone and excluding studies that reported the comparison only on intermediate-risk patients confirmed the benefit of allo-HSCT on OS. Further research should focus on individualizing allo-HSCT indications based on molecular stratification and MRD monitoring.

摘要

在首次完全缓解(CR1)期,识别适合接受异体造血干细胞移植(allo-HSCT)的儿科急性髓系白血病(AML)患者仍然存在争议。目前,基于细胞遗传学、分子生物学和微小残留病(MRD)评估,allo-HSCT 仅保留给被认为有高复发风险的患者。然而,文献中尚无比较 allo-HSCT 与其他巩固治疗类型的随机临床试验。在此,我们对比较 allo-HSCT 在 CR1 期与单独化疗作为高危儿科 AML 缓解后治疗的研究进行了最新的荟萃分析。文献检索策略确定了 9 项研究中的 10 个队列进行了治疗分析。定量合成显示 allo-HSCT 组的总生存(OS)(相对风险,1.15;95%置信区间 [CI],1.06-1.24;P=0.0006)和无病生存(DFS)(相对风险,1.31;95% CI,1.17-1.47;P=0.0001)得到改善,而化疗组的复发率增加(相对风险,1.26;95% CI,1.07-1.49;P=0.006)。包括前瞻性研究在内的敏感性分析以及排除仅报告中间风险患者比较的研究,均证实了 allo-HSCT 对 OS 的益处。进一步的研究应侧重于根据分子分层和 MRD 监测来个体化 allo-HSCT 的适应证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0191/9546991/4b476862047a/277_2022_4965_Fig1_HTML.jpg

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