Defining serum ferritin thresholds to predict clinically relevant liver iron concentrations for guiding deferasirox therapy when MRI is unavailable in patients with non-transfusion-dependent thalassaemia
Tarih
2015Yazar
Viprakasit, Vip
Taher, Ali T.
Kattamis, Antonis
Porter, John B.
Origa, Raffaella
Habr, Dany
Zhu, Zewen
Cappellini, Maria Domenica
Karakas, Zeynep
Siritanaratkul, Noppadol
Sutcharitchan, Pranee
Chuncharunee, Suporn
Üst veri
Tüm öğe kaydını gösterÖzet
Liver iron concentration (LIC) assessment by magnetic resonance imaging (MRI) remains the gold standard to diagnose iron overload and guide iron chelation therapy in patients with non-transfusion-dependent thalassaemia (NTDT). However, limited access to MRI technology and expertise worldwide makes it practical to also use serum ferritin assessments. The THALASSA (assessment of Exjade((R)) in non-transfusion-dependent THALASSemiA patients) study assessed the efficacy and safety of deferasirox in iron-overloaded NTDT patients and provided a large data set to allow exploration of the relationship between LIC and serum ferritin. Using data from screened patients and those treated with deferasirox for up to 2years, we identified clinically relevant serum ferritin thresholds (for when MRI is unavailable) for the initiation of chelation therapy (>800g/l), as well as thresholds to guide chelator dose interruption (2000g/l). (clinicaltrials.gov identifier: NCT00873041).
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