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预先存在的自身免疫性疾病对骨髓增生异常综合征结局的影响:一项人群分析。

Impact of preexisting autoimmune disease on myelodysplastic syndromes outcomes: a population analysis.

机构信息

Division of Hematology and Oncology, Larner College of Medicine at the University of Vermont, Burlington, VT.

Biomedical Statistics Research Core, University of Vermont, Burlington, VT.

出版信息

Blood Adv. 2023 Nov 28;7(22):6913-6922. doi: 10.1182/bloodadvances.2023011050.

Abstract

Preexisting autoimmune disease affects between 10% and 30% of patients with myelodysplastic syndromes (MDS). Studies comparing outcomes in patients with MDS with and without autoimmune disease show discordant results. Using the Surveillance, Epidemiology, and End Results Medicare database, we conducted a population analysis to define the impact of autoimmunity on MDS outcomes. Cases were ascertained between 2007 and 2017 and claim algorithms used to identify autoimmune disease, demographic characteristics, comorbidity scores, MDS histology, transfusion burden, treatment with hypomethylating agents, and hematopoietic stem cell transplantation. Cox regression models estimated the impact on survival, and competing-risk regression models defined the effect on leukemic transformation. We analyzed 15 277 patients with MDS, including 2442 (16%) with preexisting autoimmune disease. The epidemiologic profile was distinctive in cases with preexisting autoimmunity, who were younger, were predominantly female, and had higher transfusion burden without difference in MDS histologic distribution. Autoimmune disease was associated with 11% decreased risk of death (hazard ratio [HR], 0.89; 95% confidence interval [CI], 0.85-0.94; P < .001). The effect on risk of leukemic transformation differed based on MDS histology. In low-risk MDS histologies, autoimmunity was associated with a 1.9-fold increased risk of leukemia (HR, 1.87; 95% CI, 1.17-2.99; P = .008), whereas no significant effect was seen in other groups. These results suggest that autoimmune disease affects survival in MDS and is associated with decreased mortality. The survival effect was evident in low-risk histologies despite higher risk of progression to leukemia. This could represent inflammation-driven hematopoiesis, simultaneously favoring less aggressive phenotypes and clonal expansion, which warrants further investigation.

摘要

先前存在的自身免疫性疾病影响了 10%至 30%的骨髓增生异常综合征 (MDS) 患者。比较 MDS 患者有和无自身免疫性疾病的结局的研究结果不一致。我们使用监测、流行病学和最终结果 Medicare 数据库进行了一项人群分析,以确定自身免疫对 MDS 结局的影响。病例在 2007 年至 2017 年之间确定,使用索赔算法来识别自身免疫性疾病、人口统计学特征、合并症评分、MDS 组织学、输血负担、低甲基化剂治疗和造血干细胞移植。Cox 回归模型估计对生存的影响,竞争风险回归模型定义对白血病转化的影响。我们分析了 15277 例 MDS 患者,其中 2442 例(16%)有先前存在的自身免疫性疾病。在有先前自身免疫性疾病的病例中,流行病学特征明显,患者年龄较小、以女性为主,且输血负担较高,但 MDS 组织学分布无差异。自身免疫性疾病与死亡风险降低 11%相关(风险比 [HR],0.89;95%置信区间 [CI],0.85-0.94;P<0.001)。对白血病转化风险的影响因 MDS 组织学而异。在低危 MDS 组织学中,自身免疫与白血病风险增加 1.9 倍相关(HR,1.87;95%CI,1.17-2.99;P=0.008),而在其他组中则未见显著影响。这些结果表明,自身免疫性疾病影响 MDS 的生存,与死亡率降低相关。尽管向白血病进展的风险较高,但在低危组织学中仍可见到生存效果。这可能代表炎症驱动的造血,同时有利于侵袭性较低的表型和克隆扩增,这需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/643e/10685168/a5defc2ebfe2/BLOODA_ADV-2023-011050-ga1.jpg

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