Mini-ATG/TBI conditioning regimen facilitates cure of acquired aplastic anemia in children via unrelated umbilical cord blood transplantation

X Xia Chen Y Yuanyuan Ren Y Ye Guo Y Yang Wan (National Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine) L Lipeng Liu X Xiaoyan Zhang X Xiaolan Li X Xiaofan Zhu W Wenyu Yang (Laboratory of Advanced Materials, Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Molecular Engineering of Polymers, Collaborative Innovation Center of Chemistry for Energy Materials (2011-iChEM), College of Chemistry and Materials) F Fang Liu

Abstract

Abstract Introduction: Umbilical cord blood transplantation (UCBT) represents a alternative therapeutic option for patients with acquired aplastic anemia (AA) lacking a HLA-matched sibling donor. However, high incidences of graft failure and acute graft-versus-host disease (aGVHD) following UCBT remain major challenges. The optimal conditioning regimen for UCBT in AA is yet to be established. Methods: We enrolled patients with newly diagnosed AA or those refractory to prior Immunosuppressive therapy. This single-center prospective UCBT trial (registered at www.chictr.org.cn #ChiCTR2400088868), initiated in March 2024, compared outcomes using a mini-ATG/TBI-based regimen against historical data from our center prior to March 2024. The mini-ATG/TBI regimen comprised: rabbit ATG (rATG, 2.5 mg/kg) on day -7, total body irradiation (TBI, 3 Gy) on day -7, fludarabine (FLU, 40 mg/m²) on days -6 to -2, and cyclophosphamide (CTX, 40 mg/m²) on days -4 and -2. The historical regimen consisted of TBI (4 Gy) on day -7, FLU (40 mg/m²) on days -6 to -2, and CTX (60 mg/m²) on days -3 and -2. Outcomes evaluated included aGVHD rates, graft failure rate, engraftment rate, time to neutrophil engraftment, time to platelet engraftment, and overall survival. Results: 1.A total of 27 patients were enrolled: 18 in the mini-ATG/TBI group and 9 in the conventional group. The cohort included 13 males and 14 females, with a median age of 7 years (range: 2–15 years). No significant age difference existed between groups (P=0.166). 2.aGVHD: Grade III-IV aGVHD occurred in 2/18 patients (11.11%) and Grade I-II in 5/18 in the mini-ATG/TBI group, compared to 4/9 (44.44%) and 3/9 in the conventional group. The incidence of severe (Grade III-IV) aGVHD was significantly lower in the mini-ATG/TBI group (11.11% vs. 44.44%, P=0.05). 3.Engraftment: One patient in the mini-ATG/TBI group experienced graft failure due to early EBV viremia (within 1month post-transplant) complicated by suspected splenic PTLD and secondary hemophagocytic lymphohistiocytosis (HLH). This patient achieved disease-free survival after salvage haploidentical transplantation using an HLH-directed conditioning regimen. Engraftment was successful in the remaining 26 patients. Engraftment rates of the two groups were 94.12% vs. 100% (P=0.471). Median donor chimerism on day +7 was 71.62% (range: 21.84%–92.75%), with no significant difference between groups (72.25% vs. 63%, P=0.522). Complete donor chimerism (≥99%) was achieved by day +14 in all evaluable patients. Median time to neutrophil engraftment was 15 days (range: 12–30) in the mini-ATG/TBI group and 16 days (range: 13–27) in the conventional group (P=0.411). Median time to platelet engraftment was 25 days (range: 16–67) vs. 24 days (range: 18–36) (P=0.643). In the mini-ATG/TBI group, odd-numbered patients received avatrombopag starting on day +7 to promote platelet engraftment, while even-numbered patients received thrombopoietin (TPO). Subgroup analysis showed no significant difference in platelet engraftment time (27 days vs. 24 days; P=0.456). 4.Transplant Related Complications: Rates of sepsis, transplant-associated thrombotic microangiopathy (TA-TMA), EBV infection, and hemorrhagic cystitis did not differ significantly between two groups. However, CMV viremia incidence differed significantly (6.25% vs. 66.67%, P=0.001), attributed to the widespread use of letermovir for CMV prophylaxis after 2024. 5.Survival: The estimated 2-year overall survival (OS) rate was 92.86% (±6.88%) for the mini-ATG/TBI group and 88.89% (±10.48%) for the conventional group, showing no statistically significant difference (χ²=0.001, P=0.971). Conclusions: These data support the mini-ATG/TBI regimen as an effective conditioning approach for UCBT in acquired aplastic anemia, demonstrating particular utility in pediatric patients or low body weight adults. Key words: Aplastic Anemia; Unrelated Umbilical Cord Blood Transplantation; mini ATG

Article Details

Journal Blood
Volume / Issue Vol. 146, Issue Supplement 1
Published November 03, 2025
Pages 2420-2420
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (10)

X

Xia Chen

Y

Yuanyuan Ren

Y

Ye Guo

Y

Yang Wan

National Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine

L

Lipeng Liu

X

Xiaoyan Zhang

X

Xiaolan Li

X

Xiaofan Zhu

W

Wenyu Yang

Laboratory of Advanced Materials, Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Molecular Engineering of Polymers, Collaborative Innovation Center of Chemistry for Energy Materials (2011-iChEM), College of Chemistry and Materials

F

Fang Liu