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Azathioprine or mycophenolate mofetil for pediatric autoimmune cytopenia: a propensity score-matched study
Thomas Pincez1,2, Helder Fernandes1,3, Guy Leverger4
1Centre de Référence National des Cytopénies Auto-immunes de l'Enfant, Bordeaux, France.
Abstract:
Data on the immunosuppressants azathioprine (AZA) and mycophenolate mofetil (MMF) in autoimmune cytopenia (AIC) are limited, and no direct comparison exists. We analyzed the failure-free survival (FFS; time from AZA/MMF initiation to another non-first-line treatment, or death) of both treatments in the prospective nationwide pediatric OBS'CEREVANCE cohort. We included 343 patients (chronic immune thrombocytopenia, n = 161; autoimmune hemolytic anemia, n = 74; Evans syndrome, n = 108). They received AZA (n = 276) or MMF (n = 104; 37 sequentially received both) as monotherapy for a median duration of 11.3 (range, 0.01-149.0) months. Older age was associated with higher FFS for AZA, whereas secondary AIC was associated with higher FFS for MMF. AIC type had no effect. In a propensity score (PS)-matched cohort, AZA and MMF showed similar FFS (adjusted hazard ratio, 0.91; 95% confidence interval, 0.54-1.52; P = .71), with 1-year FFS rates of 73% and 76%, respectively. In subgroup analyses, AZA was associated with higher FFS in PS-matched patients diagnosed at an age of ≥10 years, whereas MMF was associated with higher FFS in PS-matched patients diagnosed at an age of <10 years and in those with confirmed secondary AIC (although with suboptimal matching). Rates of grade ≥3 infection were similar between the 2 drugs, at ∼2% new cases per year. In summary, AZA and MMF demonstrated comparable overall FFS and infection risk. However, our data suggest that AZA may be more beneficial in children diagnosed at an age of ≥10 years, whereas MMF may be more beneficial in those diagnosed at an age of <10 years and possibly in patients with secondary AIC.
Insights
Azathioprine (AZA) and mycophenolate mofetil (MMF) show similar effectiveness and safety for treating pediatric autoimmune cytopenias (AIC). However, AZA may be better for older children, while MMF suits younger children and those with secondary AIC.
Area of Science:
- Pediatric Hematology
- Immunology
- Pharmacology
Background:
- Limited data exists on azathioprine (AZA) and mycophenolate mofetil (MMF) for autoimmune cytopenias (AIC).
- No direct comparison of AZA and MMF in pediatric AIC populations has been performed.
Purpose of the Study:
- To compare the failure-free survival (FFS) of AZA versus MMF in pediatric AIC.
- To identify patient subgroups that may benefit more from AZA or MMF.
Main Methods:
- Analysis of the prospective nationwide pediatric OBS'CEREVANCE cohort (n=343).
- Comparison of FFS between AZA and MMF using propensity score matching.
- Subgroup analyses based on age at diagnosis and AIC type.
Main Results:
- Overall, AZA and MMF demonstrated comparable FFS (1-year FFS: 73% vs. 76%) and similar rates of severe infections (approx. 2% per year).
- Older age (≥10 years) was associated with higher FFS for AZA.
- Younger age (<10 years) and secondary AIC were associated with higher FFS for MMF.
Conclusions:
- Azathioprine and mycophenolate mofetil are comparable in overall efficacy and safety for pediatric AIC.
- Treatment choice may be guided by age: AZA for older children (≥10 years) and MMF for younger children (<10 years).
- Mycophenolate mofetil may be preferred for patients with secondary autoimmune cytopenias.
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