Secondary autoimmune diseases occurring after HSCT for an autoimmune disease: a retrospective study of the EBMT Autoimmune Disease Working Party - PubMed
- ️Sat Jan 01 2011
. 2011 Aug 11;118(6):1693-8.
doi: 10.1182/blood-2011-02-336156. Epub 2011 May 19.
Myriam Labopin, Massimo Di Gioia, Mario Abinun, Tobias Alexander, Irene Miniati, Francesca Gualandi, Athanasios Fassas, Thierry Martin, Carl Philipp Schwarze, Nico Wulffraat, Maya Buch, Antonia Sampol, Enric Carreras, Benedicte Dubois, Bernd Gruhn, Tayfun Güngör, David Pohlreich, Annemie Schuerwegh, Emilian Snarski, John Snowden, Paul Veys, Anders Fasth, Stig Lenhoff, Chiara Messina, Jan Voswinkel, Manuela Badoglio, Jörg Henes, David Launay, Alan Tyndall, Eliane Gluckman, Dominique Farge; EBMT Autoimmune Disease Working Party
Affiliations
- PMID: 21596847
- DOI: 10.1182/blood-2011-02-336156
Free article
Secondary autoimmune diseases occurring after HSCT for an autoimmune disease: a retrospective study of the EBMT Autoimmune Disease Working Party
Thomas Daikeler et al. Blood. 2011.
Free article
Abstract
To specify the incidence and risk factors for secondary autoimmune diseases (ADs) after HSCT for a primary AD, we retrospectively analyzed AD patients treated by HSCT reported to EBMT from 1995 to 2009 with at least 1 secondary AD (cases) and those without (controls). After autologous HSCT, 29 of 347 patients developed at least 1 secondary AD within 21.9 (0.6-49) months and after allogeneic HSCT, 3 of 16 patients. The observed secondary ADs included: autoimmune hemolytic anemia (n = 3), acquired hemophilia (n = 3), autoimmune thrombocytopenia (n = 3), antiphospholipid syndrome (n = 2), thyroiditis (n = 12), blocking thyroid-stimulating hormone receptor antibody (n = 1), Graves disease (n = 2), myasthenia gravis (n = 1), rheumatoid arthritis (n = 2), sarcoidosis (n = 2), vasculitis (n = 1), psoriasis (n = 1), and psoriatic arthritis (n = 1). After autologous HSCT for primary AD, the cumulative incidence of secondary AD was 9.8% ± 2% at 5 years. Lupus erythematosus as primary AD, and antithymocyte globulin use plus CD34(+) graft selection were important risk factors for secondary AD by multivariate analysis. With a median follow-up of 6.2 (0.54-11) years after autologous HSCT, 26 of 29 patients with secondary AD were alive, 2 died during their secondary AD (antiphospholipid syndrome, hemophilia), and 1 death was HSCT-related. This European multicenter study underlines the need for careful management and follow-up for secondary AD after HSCT.
Comment in
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HSCT for AID: entering prime time?
Pavletic SZ. Pavletic SZ. Blood. 2011 Aug 11;118(6):1438-9. doi: 10.1182/blood-2011-06-356576. Blood. 2011. PMID: 21835965 No abstract available.
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