Comparison of haploidentical hematopoietic stem cell transplantation with chemotherapy in older adults with acute myeloid leukemia

被引:4
|
作者
Sun, Yu-Qian [1 ,2 ]
Zhang, Xiao-Hui [1 ,2 ]
Jiang, Qian [1 ,2 ]
Jiang, Hao [1 ,2 ]
Chang, Ying-Jun [1 ,2 ]
Wang, Yu [1 ,2 ]
Xu, Lan-Ping [1 ,2 ]
Liu, Kai-Yan [1 ,2 ]
Huang, Xiao-Jun [1 ,2 ]
机构
[1] Peking Univ, Peking Univ Peoples Hosp, Natl Clin Res Ctr Treatment Hematol Dis, Inst Hematol, Beijing, Peoples R China
[2] Beijing Key Lab Hematopoiet Stem Cell Transplantat, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
1ST COMPLETE REMISSION; ALLOGENEIC TRANSPLANTATION; POSTREMISSION TREATMENT; CYCLOPHOSPHAMIDE; FLUDARABINE; REGIMENS; OUTCOMES; DONOR; MRD;
D O I
10.1038/s41409-023-01925-5
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Acute myeloid leukemia (AML) outcomes are very poor in older patients. Haploidentical stem cell transplantation (haplo-SCT) helps to achieve long-term survival. However, the benefit of haplo-SCT versus chemotherapy is unclear in older adults with AML. Outcomes were retrospectively compared among patients aged 55-65 years for chemotherapy consolidation or haplo-SCT for AML in the first complete remission with intermediate to high-risk disease. Forty-six patients who underwent chemotherapy and 38 patients who underwent haplo-SCT were evaluated in the final analysis. Compared with the chemotherapy group, patients in the haplo-SCT group had significantly better overall survival (OS) (74.0% versus 23.9% at 36 months, p = 0.005) and leukemia-free survival (LFS) (74.0% versus 21.6%, p < 0.001). The cumulative incidence of relapse (CIR) was significantly lower in the haplo-SCT group (17.3% versus 75.4%, p < 0.001). Treatment-related mortality (TRM) was similar in the haplo-SCT and chemotherapy groups (7.9% versus 4.8%, p = 0.587). In the multivariate analysis, haplo-SCT was associated with improved OS, LFS, and decreased CIR. Haplo-SCT did not affect TRM. In conclusion, our data suggest that haploidentical transplant may be an alternative to consolidation chemotherapy as post-remission therapy in patients with intermediate or high-risk AML aged 55-65 years. Further well-designed studies are needed to validate this result.
引用
收藏
页码:491 / 497
页数:7
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