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

  • 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

摘要

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.