Acquired factor X deficiency in patients with amyloid light-chain amyloidosis: incidence, bleeding manifestations, and response to high-dose chemotherapy
Eb. Choufani et al., Acquired factor X deficiency in patients with amyloid light-chain amyloidosis: incidence, bleeding manifestations, and response to high-dose chemotherapy, BLOOD, 97(6), 2001, pp. 1885-1887
Acquired deficiency of factor X occurs in patients with systemic amyloid li
ght-chain (AL) amyloidosis, presumably due to adsorption of factor X to amy
loid fibrils, Of 368 consecutive patients with systemic AL amyloidosis eval
uated at Boston Medical Center, 32 patients (8.7%) had factor X levels belo
w 50% of normal, Eighteen of these patients (56%) had bleeding complication
s, which were more frequent and severe in the 12 patients below 25% of norm
al; 2 episodes were fatal, Ten factor X-deficient patients received high-do
se melphalan chemotherapy followed by autologous stem cell transplantation.
Of 7 patients alive 1 year after treatment, 4 had a complete hematologic r
esponse, and all 4 experienced improvement in their factor 4 levels, One of
2 additional patients with partial hematologic responses had improvement i
n factor X, Thus, aggressive treatment of the underlying plasma cell dyscra
sia in AL amyloidosis can lead to the amelioration of amyloid-related facto
r X deficiency. (Blood, 2001;97: 1885-1887) (C) 2001 by The American Societ
y of Hematology.