Zeng Xiangzong, Xuan Li, Fan Zhiping, Zhang Yu, Zhao Ke, Zhou Ya, Xu Jun, Liu Qifa, Dai Min
Department of Hematology, Nanfang Hospital, Southern Medical University, 1838 Guangzhou Blvd North, Guangzhou, China.
Exp Hematol Oncol. 2021 Aug 14;10(1):44. doi: 10.1186/s40164-021-00238-x.
Myelofibrosis (MF) may serve as a poor prognostic factor in myelodysplastic syndromes (MDS). This study explored the impact of allogeneic hematopoietic stem cell transplantation (allo-HSCT) on the outcome of MDS patients with MF.
Three hundred and sixteen MDS patients were enrolled in this retrospective study. Based on the degree of MF, we divided the patients into 2 groups: grade 0-1 (MF-0/1) and grade 2-3 (MF-2/3) groups. The clinical features, treatments, and prognosis in MDS patients with MF were analyzed.
Forty-three (13.6%) patients were diagnosed as MF-2/3. Complex karyotypes were more common in the MF-2/3 compared to MF-0/1 groups (P = 0.002). The overall response rate (ORR) of cytoreduction was 49.0%, along with 53.3% in the MF-0/1 and 16.7% in MF-2/3 groups (P = 0.017). In total, 141 patients underwent allo-HSCT, including 121 in the MF-0/1 and 20 in MF-2/3 groups. The median time to neutrophil reconstruction was 12 (range: 7-34) and 14 (range: 10-45) days (P = 0.005), and platelet reconstruction was 14 (range: 8-68) and 18 (range: 8-65) days (P = 0.045) in the MF-0/1 and MF-2/3 groups, respectively. However, the cumulative incidence of neutrophil and platelet engraftment achieved at day + 30 was not different between the two groups (P = 0.107, P = 0.303, respectively). Non-relapse mortality, relapse, and acute and chronic graft-versus-host disease were similar between the two groups (all P > 0.05). Among patients with allo-HSCT, the 2-year overall survival (OS) was 68.5% (95% CI: 60.1-76.9%) and 68.4% (95% CI: 47.4-89.4%) in the MF-0/1 and MF-2/3 groups, respectively, (P = 0.636). Among patients without allo-HSCT, the 2-year OS was 49.9% (95% CI: 40.7-59.1%) and 19.2% (95% CI: 0-39.6%) in the MF-0/1 and MF-2/3 groups, respectively, (P = 0.002). In multivariate cox analysis, complex karyotype was an unfavorable factor for relapse (HR, 4.16; P = 0.006), disease-free survival (DFS) (HR, 2.16; P = 0.020), and OS (HR, 2.47; P = 0.009) post-transplantation.
Patients with MF-2/3 have more complex karyotypes and lower ORR of cytoreduction in MDS. Among patients without allo-HSCT, patients with MF-2/3 have a worse prognosis than those with MF-0/1. However, the adverse impact of MF on prognosis may be overcome by allo-HSCT.
骨髓纤维化(MF)可能是骨髓增生异常综合征(MDS)的不良预后因素。本研究探讨了异基因造血干细胞移植(allo-HSCT)对合并MF的MDS患者预后的影响。
316例MDS患者纳入本回顾性研究。根据MF程度,将患者分为2组:0-1级(MF-0/1)组和2-3级(MF-2/3)组。分析合并MF的MDS患者的临床特征、治疗及预后。
43例(13.6%)患者诊断为MF-2/3。与MF-0/1组相比,MF-2/3组复杂核型更常见(P = 0.002)。细胞减少的总缓解率(ORR)为49.0%,MF-0/1组为53.3%,MF-2/3组为16.7%(P = 0.017)。共有141例患者接受了allo-HSCT,其中MF-0/1组121例,MF-2/3组20例。MF-0/1组和MF-2/3组中性粒细胞重建的中位时间分别为12天(范围:7-34天)和14天(范围:10-45天)(P = 0.005),血小板重建的中位时间分别为14天(范围:8-68天)和18天(范围:8-65天)(P = 0.045)。然而,两组在+30天时中性粒细胞和血小板植入的累积发生率无差异(分别为P = 0.107,P = 0.303)。两组间非复发死亡率、复发率以及急慢性移植物抗宿主病相似(所有P>0.05)。在接受allo-HSCT的患者中,MF-0/1组和MF-2/3组的2年总生存率(OS)分别为68.5%(95%CI:60.1-76.9%)和68.4%(95%CI:47.4-89.4%)(P = 0.636)。在未接受allo-HSCT的患者中,MF-0/1组和MF-2/3组的2年OS分别为49.9%(95%CI:40.7-59.1%)和19.2%(95%CI:0-39.6%)(P = 0.002)。在多因素cox分析中,复杂核型是移植后复发(HR,4.16;P = 0.006)、无病生存(DFS)(HR,2.16;P = 0.020)和OS(HR,2.47;P = 0.009)的不利因素。
MF-2/3的MDS患者核型更复杂,细胞减少的ORR更低。在未接受allo-HSCT的患者中,MF-2/3的患者比MF-0/1的患者预后更差。然而,allo-HSCT可能克服MF对预后的不利影响。