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亲缘单倍体造血细胞移植后预防性供者淋巴细胞输注和移植后环磷酰胺治疗儿童高危髓系肿瘤:一项回顾性研究。

Prophylactic donor lymphocyte infusion after haploidentical hematopoietic cell transplantation and post-transplant cyclophosphamide for treatment of high-risk myeloid neoplasms in children: A retrospective study.

机构信息

Laboratory of Pediatric Hematology, Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Department of Hematology, Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Pediatr Blood Cancer. 2023 Nov;70(11):e30659. doi: 10.1002/pbc.30659. Epub 2023 Sep 5.

Abstract

BACKGROUND

Post-transplant cyclophosphamide (PTCy) has been recommended for prevention of graft-versus-host disease (GvHD) following haploidentical hematopoietic cell transplantation (haplo-HCT) for treatment of malignant blood diseases, but disease relapse remains a problem. Although donor lymphocyte infusion (DLI) is reported to be effective for treating post-transplantation relapse, the efficacy and safety of prophylactic-DLI (pro-DLI) post haplo-HCT, and PTCy in pediatric patients with hematological malignancies is unknown.

METHODS

We retrospectively analyzed the outcomes of 54 pediatric patients with high-risk myeloid neoplasms who received a PTCy regimen for GvHD prophylaxis and pro-DLI after haploidentical peripheral blood stem cell transplantation. The high-risk myeloid neoplasms in this cohort included acute myeloid leukemia (n = 46) and myelodysplastic syndromes (n = 8).

RESULTS

Median follow-up was for 19.7 (range: 3.4-46.6) months. The cumulative incidences of grade II-IV and III-IV acute GvHD were 37.0% (95% CI: 22.7%-48.7%) and 16.7% (95% CI: 6.1%-26.0%), respectively. There were no graft-failure events, and the 2-year rate of moderate/severe chronic GvHD was 8.1% (95% CI: 0%-16.7%). The 2-year non-relapse mortality, relapse, disease-free survival, GvHD-free relapse-free survival, and overall survival rates were 5.1% (95% CI: 0%-11.7%), 16.6% (95% CI: 5.3%-26.6%), 78.9% (95% CI: 68.0%-91.6%), 62.2% (95% CI: 49.4%-78.3%), and 87.3% (95% CI: 78.3%-97.4%), respectively.

CONCLUSIONS

Prophylactic donor lymphocyte infusion in the setting of haploidentical hematopoietic cell transplantation with post-transplant cyclophosphamide appears to be effective and safe in pediatric patients with high-risk myeloid neoplasms.

摘要

背景

环磷酰胺(PTCy)在用于治疗恶性血液病的单倍体造血细胞移植(haplo-HCT)后,已被推荐用于预防移植物抗宿主病(GvHD),但疾病复发仍然是一个问题。虽然报道供者淋巴细胞输注(DLI)对治疗移植后复发有效,但在儿科血液病患者中,haplo-HCT 后预防性-DLI(pro-DLI)和 PTCy 的疗效和安全性尚不清楚。

方法

我们回顾性分析了 54 例接受 PTCy 方案预防 GvHD 并在单倍体外周血干细胞移植后接受 pro-DLI 的高危髓系肿瘤儿科患者的结果。该队列中的高危髓系肿瘤包括急性髓系白血病(n=46)和骨髓增生异常综合征(n=8)。

结果

中位随访时间为 19.7 个月(范围:3.4-46.6)。Ⅱ-Ⅳ级和Ⅲ-Ⅳ级急性 GvHD 的累积发生率分别为 37.0%(95%CI:22.7%-48.7%)和 16.7%(95%CI:6.1%-26.0%)。无移植物衰竭事件,2 年时中重度慢性 GvHD 的发生率为 8.1%(95%CI:0%-16.7%)。2 年非复发死亡率、复发率、无病生存率、无 GvHD 复发无病生存率和总生存率分别为 5.1%(95%CI:0%-11.7%)、16.6%(95%CI:5.3%-26.6%)、78.9%(95%CI:68.0%-91.6%)、62.2%(95%CI:49.4%-78.3%)和 87.3%(95%CI:78.3%-97.4%)。

结论

在单倍体造血细胞移植中应用 PTCy 后预防性输注供者淋巴细胞似乎在儿科高危髓系肿瘤患者中是有效且安全的。

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