Early Allogeneic Transplantation Favorably Influences the Outcome of Pediatric Acute Myeloid Leukemia-A Retrospective Study in a Single Center Over 2 Decades

被引:0
|
作者
Lo, Tzu-Ya [1 ,5 ]
Wang, Yi-Lun [2 ,3 ]
Jaing, Tang-Her [2 ,3 ]
Chang, Tsung-Yen [2 ,3 ]
Wen, Yu-Chuan [4 ]
Chiu, Chia-Chi [4 ]
Hsiao, Yi-Wen [4 ]
Chen, Shih-Hsiang [2 ,3 ]
机构
[1] Chang Gung Univ, Chang Gung Mem Hosp, Taoyuan, Taiwan
[2] Chang Gung Univ, Chang Gung Mem Hosp, Dept Pediat, Div Hematol, Taoyuan, Taiwan
[3] Chang Gung Univ, Chang Gung Mem Hosp, Dept Pediat, Div Oncol, Taoyuan, Taiwan
[4] Chang Gung Mem Hosp, Dept Nursing, Taoyuan, Taiwan
[5] Chang Gung Univ, Chang Gung Mem Hosp, 5 Fu Shin St, Taoyuan 33305, Taiwan
关键词
STEM-CELL TRANSPLANTATION; REDUCED RISK; 1ST; REACTIVATION; CHILDREN; RELAPSE;
D O I
10.1016/j.transproceed.2023.11.030
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Transplantation advancements offer the potential for improving the prognosis of patients with acute myeloid leukemia (AML). Controversies surrounding indications and timing persist. We focused on identifying prognostic factors and exploring the advantages of early transplantation. Patients and Methods. We studied 102 pediatric patients with AML (February 1999 -August 2022), using Cox regression to analyze survival and hematopoietic cell transplantation (HCT) outcomes and Kaplan-Meier curves to assess HCT timing's impact on prognosis. Results. "Treatment in First Complete Remission [CR1]: Chemotherapy" showed increased risk in multivariate and univariate Cox regression analyses, whereas "HCT during the study period" displayed divergent outcomes. Focusing on transplanted patients, "Treatment in CR1: Chemotherapy" still correlated with higher mortality risk. These findings emphasize the pivotal role of the treatment strategy adopted in CR1 on overall survival rather than HCT alone. Donor cytomegalovirus (CMV) positivity is also related to reduced mortality risk. Kaplan-Meier analysis supported superior 5-year survival rates with "HCT" compared with "chemotherapy" in CR1. In the 3-arm analysis, "HCT in CR1" demonstrated better 5-year overall survival (OS) and 5year disease-free survival (DFS) compared with "Never HCT," whereas "HCT in CR2" had the least favorable prognosis (5-year OS: 79.2% vs 57.1% vs 50%, P = .056; 5-year DFS: 73.6% vs 55.2% vs 0%, P = .000). Conclusion. Our study highlights the benefits of transplantation during CR1 on prognosis. However, when contemplating CR1 transplantation recommendations, evaluation of various factors, such as the patient's clinical state, relapse risk, transplant-related mortality, CMV status, and other pertinent considerations, is vital. Comprehensive case discussions with patients and families are demanded in optimizing treatment.
引用
收藏
页码:201 / 210
页数:10
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