Outcomes of allogeneic hematopoietic stem cell transplantation versus intensive chemotherapy in patients with myeloid sarcoma: a nationwide representative multicenter study.

IF 4.5 2区 医学 Q1 HEMATOLOGY Bone Marrow Transplantation Pub Date : 2024-12-02 DOI:10.1038/s41409-024-02485-y
Jie Sun, Yi-Cheng Zhang, Jia Wei, Ya-Jing Xu, Yue Zhang, Yu-Hua Li, An-Qin Wu, Lei Fan, Yu Zhu, Feng-Qi Liu, Zhong-Xing Jiang, Chao Liu, Ming Jiang, Jian-Hua Qu, Peng-Cheng He, Jie Wang, Xiao-Bing Huang, Rong Xiao, Su-Jun Gao, Qiang Guo, San-Bin Wang, Xiao-Ping Li, Sheng-Jin Fan, Li-Li Sun, Lan-Ping Xu, Xiao-Jun Huang, Xiao-Hui Zhang
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Abstract

Myeloid sarcoma (MS) is a rare hematological neoplasm with poor prognosis, posing a significant clinical challenge due to the absence of effective and standardized treatments. We conducted a retrospective analysis of 162 MS patients treated at 12 centers to compare outcomes between intensive chemotherapy and allogeneic hematopoietic stem cell transplantation (allo-HSCT). Our analysis revealed that allo-HSCT demonstrated superior overall survival (OS) within the initial 36 months compared to intensive chemotherapy alone (p = 0.037). However, beyond 36 months (36-60 months), a reverse trend was observed (p = 0.056). Subgroup analysis revealed potential benefit for isolated MS patients with allo-HSCT, but not for those with leukemic MS. Additionally, in patients achieving first complete remission (CR1) after induction chemotherapy, allo-HSCT did not significantly improve 5-year OS compared with intensive chemotherapy alone (p = 0.25). Conversely, allo-HSCT significantly improved 5-year OS in non-CR1 patients (p < 0.001). Notably, HLA-matched HSCT and haploidentical HSCT showed comparable outcomes in terms of OS, disease-free survival, and cumulative incidence of relapse. In conclusion, allo-HSCT improved outcomes for MS patients within 36 months of disease onset, and haploidentical HSCT emerged as a viable treatment option for patients without matched donors.

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骨髓肉瘤患者异体造血干细胞移植与强化化疗的结果:一项具有全国代表性的多中心研究。
髓系肉瘤(Myeloid sarcoma, MS)是一种罕见的血液学肿瘤,预后较差,由于缺乏有效和规范的治疗方法,给临床带来了重大挑战。我们对12个中心治疗的162例MS患者进行了回顾性分析,比较强化化疗和同种异体造血干细胞移植(alloo - hsct)的结果。我们的分析显示,与单独强化化疗相比,同种异体造血干细胞移植在最初的36个月内表现出更高的总生存期(OS) (p = 0.037)。然而,超过36个月(36-60个月),观察到相反的趋势(p = 0.056)。亚组分析显示,接受同种异体造血干细胞移植对孤立的多发性硬化症患者有潜在的益处,但对白血病多发性硬化症患者则没有。此外,在诱导化疗后首次完全缓解(CR1)的患者中,与单纯强化化疗相比,同种异体造血干细胞移植并没有显著改善5年OS (p = 0.25)。相反,同种异体造血干细胞移植显著改善了非cr1患者的5年OS (p
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来源期刊
Bone Marrow Transplantation
Bone Marrow Transplantation 医学-免疫学
CiteScore
8.40
自引率
8.30%
发文量
337
审稿时长
6 months
期刊介绍: Bone Marrow Transplantation publishes high quality, peer reviewed original research that addresses all aspects of basic biology and clinical use of haemopoietic stem cell transplantation. The broad scope of the journal thus encompasses topics such as stem cell biology, e.g., kinetics and cytokine control, transplantation immunology e.g., HLA and matching techniques, translational research, and clinical results of specific transplant protocols. Bone Marrow Transplantation publishes 24 issues a year.
期刊最新文献
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