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Use of Hematopoietic Stem Cell Transplantation to Assess the Origin of Myelodysplastic Syndrome
Published on: October 3, 2018
Impact of preexisting autoimmune disease on myelodysplastic syndromes outcomes: a population analysis
Diego Adrianzen-Herrera1, Andrew D Sparks2, Rohit Singh1
1Division of Hematology and Oncology, Larner College of Medicine at the University of Vermont, Burlington, VT.
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.
Insights
Preexisting autoimmune disease in myelodysplastic syndromes (MDS) patients is linked to decreased mortality. However, it increases leukemia risk in low-risk MDS subtypes, suggesting complex inflammation-driven effects.
Area of Science:
- Hematology
- Immunology
- Oncology
Background:
- Autoimmune diseases affect 10-30% of myelodysplastic syndromes (MDS) patients.
- Previous studies on autoimmunity's impact on MDS outcomes have yielded conflicting results.
- Understanding this relationship is crucial for patient management and prognosis.
Purpose of the Study:
- To investigate the impact of preexisting autoimmune disease on survival and leukemic transformation in patients with MDS.
- To analyze demographic and clinical characteristics associated with autoimmunity in MDS.
- To explore potential mechanisms underlying the observed effects.
Main Methods:
- Population-based analysis using the Surveillance, Epidemiology, and End Results (SEER) Medicare database (2007-2017).
- Identification of autoimmune disease using claim algorithms.
- Cox regression and competing-risk regression models to assess survival and leukemic transformation.
- Analysis of 15,277 MDS patients, including 2,442 with autoimmune disease.
Main Results:
- Patients with autoimmune disease were younger, predominantly female, and had a higher transfusion burden.
- Autoimmune disease was associated with an 11% decreased risk of death (HR, 0.89; P < .001).
- In low-risk MDS, autoimmunity increased leukemia risk (HR, 1.87; P = .008), but not in other subtypes.
Conclusions:
- Preexisting autoimmune disease in MDS is associated with improved survival, despite an increased risk of leukemic transformation in specific subtypes.
- The findings suggest a potential role for inflammation-driven hematopoiesis.
- Further research is warranted to elucidate the complex interplay between autoimmunity, inflammation, and MDS progression.
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