The last abstract that I would like to mention is a poster presentation from our group on acquired factor X deficiency, a rare complication of AL amyloidosis. And in this, this is a retrospective study from our database of 1,956 patients with AL amyloidosis who underwent systematic screening of factor X levels. About 4.4% or 88 patients were diagnosed with factor X levels of less than 50%...
The last abstract that I would like to mention is a poster presentation from our group on acquired factor X deficiency, a rare complication of AL amyloidosis. And in this, this is a retrospective study from our database of 1,956 patients with AL amyloidosis who underwent systematic screening of factor X levels. About 4.4% or 88 patients were diagnosed with factor X levels of less than 50%. The median factor X level was 39% and the bleeding complications did not really occur in about 45% of patients. However, the rest of the patients did have some bleeding complications. Majority were mucocutaneous bleeding but about 16% did have GI bleeding and 9% had post-procedural bleeding.
Hematologic CR achievement for the underlying plasma cell dyscrasia clone did lead to improvement in factor X deficiency or tear factor X levels and the median improvement of greater than 50% did occur in 75% of patients following treatment and this was irrespective of what type of treatment was used.
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