Sun Jie, Zhang Yi-Cheng, Wei Jia, Xu Ya-Jing, Zhang Yue, Li Yu-Hua, Wu An-Qin, Fan Lei, Zhu Yu, Liu Feng-Qi, Jiang Zhong-Xing, Liu Chao, Jiang Ming, Qu Jian-Hua, He Peng-Cheng, Wang Jie, Huang Xiao-Bing, Xiao Rong, Gao Su-Jun, Guo Qiang, Wang San-Bin, Li Xiao-Ping, Fan Sheng-Jin, Sun Li-Li, Xu Lan-Ping, Huang Xiao-Jun, Zhang Xiao-Hui
Peking University People's Hospital, Peking University Institute of Hematology, Beijing, China.
Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Bone Marrow Transplant. 2025 Mar;60(3):319-325. doi: 10.1038/s41409-024-02485-y. Epub 2024 Dec 2.
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.
髓系肉瘤(MS)是一种预后较差的罕见血液肿瘤,由于缺乏有效且标准化的治疗方法,给临床带来了重大挑战。我们对在12个中心接受治疗的162例MS患者进行了回顾性分析,以比较强化化疗和异基因造血干细胞移植(allo-HSCT)的疗效。我们的分析显示,与单纯强化化疗相比,allo-HSCT在疾病初始36个月内的总生存期(OS)更优(p = 0.037)。然而,在36个月之后(36 - 60个月),观察到了相反的趋势(p = 0.056)。亚组分析显示,allo-HSCT对孤立性MS患者有潜在益处,但对白血病性MS患者则不然。此外,在诱导化疗后达到首次完全缓解(CR1)的患者中,与单纯强化化疗相比,allo-HSCT并未显著改善5年总生存期(p = 0.25)。相反,allo-HSCT在非CR1患者中显著改善了5年总生存期(p < 0.001)。值得注意的是,在总生存期、无病生存期和复发累积发生率方面,HLA匹配的HSCT和单倍体相合HSCT显示出相当的疗效。总之,allo-HSCT改善了疾病发病36个月内MS患者的预后,单倍体相合HSCT成为了没有匹配供体患者的一种可行治疗选择。