Frontiers in Pediatrics (Sep 2015)

Evans syndrome in children. Long-term outcome in a prospective French national observational cohort.

  • Nathalie eAladjidi,
  • Nathalie eAladjidi,
  • Nathalie eAladjidi,
  • Helder eFernandes,
  • Helder eFernandes,
  • Thierry eLeblanc,
  • Thierry eLeblanc,
  • Amelie eVareliette,
  • Frédéric eRieux-Laucat,
  • Yves eBertrand,
  • Hervé eChambost,
  • Marlène ePasquet,
  • Françoise eMazingue,
  • Corinne eGuitton,
  • Isabelle ePellier,
  • Françoise eRoqueplan-Bellmann,
  • Corinne eArmari-Alla,
  • Caroline eThomas,
  • Aude eMarie-Cardine,
  • Odile eLejars,
  • Fanny eFouyssac,
  • Sophie eBayart,
  • Patrick eLutz,
  • Christophe ePiguet,
  • Eric eJeziorski,
  • Eric eJeziorski,
  • Pierre eRohrlich,
  • Philippe eLemoine,
  • Damien eBodet,
  • Catherine ePaillard,
  • Gerard eCouillault,
  • Frédéric eMillot,
  • Alain eFischer,
  • Alain eFischer,
  • Yves ePerel,
  • Yves ePerel,
  • Yves ePerel,
  • Guy eLeverger,
  • Guy eLeverger

DOI
https://doi.org/10.3389/fped.2015.00079
Journal volume & issue
Vol. 3

Abstract

Read online

Evans syndrome (ES) is a rare autoimmune disorder whose long-term follow-up characteristics are unknown. Patients under 18 at the time of diagnosis of a first autoimmune cytopenia have been included since 2004 in a national prospective observational cohort. In 2014, 156 children diagnosed between 1981 and 2014 with ES, were analyzed. The median age at initial cytopenia was 5.4 (0.2-17.2) years old. For 85 sequential cases, the median delay between the episodes of AIHA and ITP was 2.4 years (0.1–16.3). The median follow-up since ES diagnosis was 6.5 years (0.1-28.8). ES revealed underlying diseases in 10% of children; in 60% of patients, various associated immune manifestations were observed, and ES remained primary in 30%. Five-year ITP and AIHA relapse-free survival were respectively 25% and 61%. In all, 69% of children required one or more than one second-line immune treatment and 15 patients (10%) died at a median age of 14.3 years (1.7-28.1).This national work provides the first consistent clinical description for ES and underscores the high percentage of associated immune manifestations, the long-term complications, and treatment toxicities. Current challenges include the identification of underlying genetic immune dysregulations and better characterization of subgroups of patients and of second-line therapy strategies.

Keywords