Kharfan-Dabaja Mohamed A, Reljic Tea, Murthy Hemant S, Ayala Ernesto, Kumar Ambuj
Division of Hematology-Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, FL.
Program for Comparative Effectiveness Research, Morsani College of Medicine, University of South Florida, Tampa, FL.
Clin Lymphoma Myeloma Leuk. 2018 Nov;18(11):703-709.e1. doi: 10.1016/j.clml.2018.07.295. Epub 2018 Aug 2.
It is common practice to refer patients to transplantation centers for allogeneic hematopoietic cell transplantation (allo-HCT) for blastic plasmacytoid dendritic-cell neoplasm (BPDCN) despite lack of randomized controlled trials. We performed a systematic review to assess the totality of evidence pertaining to the efficacy of allo-HCT in BPDCN.
We searched the Cochrane, PubMed, and Embase databases through January 5, 2018, for studies on allo-HCT for BPDCN. Two authors independently reviewed all references for inclusion and extracted data related to benefits (overall [OS] and progression-free/disease-free [PFS/DFS] survival) and harms (relapse and nonrelapse mortality) from included studies. When appropriate, data were pooled using random-effects model.
Four studies (128 patients) were included in analysis. Pooled OS rate was 50% (95% confidence interval [CI], 41-59) for all patients. Among patients who underwent allografting whose disease was in first complete remission (CR1), pooled OS and PFS/DFS rates were 67% (95% CI, 52-80) and 53% (95% CI, 29-76), respectively. For patients who underwent allografting in > CR1, pooled OS and PFS/DFS rates were 7% (95% CI, 0-32) for both outcomes. Relapse rates were higher when reduced-intensity regimens were used (40% [95% CI, 25-56] vs. 18% [95% CI, 7-31]).
This systematic review represents the best available evidence supporting allo-HCT in BPDCN, especially when offered in CR1. Use of myeloablative allo-HCT results in lower pooled relapse rates (18% vs. 40%). A prospective comparative study will be needed to determine the impact of intensity of the conditioning regimen on postallograft relapse.
尽管缺乏随机对照试验,但将原发性浆细胞样树突状细胞瘤(BPDCN)患者转诊至移植中心进行异基因造血细胞移植(allo-HCT)仍是常见做法。我们进行了一项系统评价,以评估与allo-HCT治疗BPDCN疗效相关的全部证据。
我们检索了截至2018年1月5日的Cochrane、PubMed和Embase数据库,以查找关于allo-HCT治疗BPDCN的研究。两位作者独立审查所有参考文献以确定是否纳入,并从纳入研究中提取与获益(总生存期[OS]和无进展/无病生存期[PFS/DFS])和危害(复发和非复发死亡率)相关的数据。在适当情况下,使用随机效应模型汇总数据。
四项研究(128例患者)纳入分析。所有患者的汇总OS率为50%(95%置信区间[CI],41-59)。在疾病处于首次完全缓解(CR1)时接受同种异体移植的患者中,汇总OS率和PFS/DFS率分别为67%(95%CI,52-80)和53%(95%CI,29-76)。对于在>CR1时接受同种异体移植的患者,两种结局的汇总OS率和PFS/DFS率均为7%(95%CI,0-32)。使用减低强度方案时复发率更高(40%[95%CI,25-56]对18%[95%CI,7-31])。
这项系统评价代表了支持在BPDCN中进行allo-HCT的最佳现有证据,尤其是在CR1时进行。清髓性allo-HCT的使用导致较低的汇总复发率(18%对40%)。需要进行一项前瞻性比较研究来确定预处理方案强度对移植后复发的影响。