K. Fujimura et al., RECOMBINANT HUMAN INTERFERON-ALPHA-2B (RH IFN-ALPHA-2B) THERAPY FOR STEROID-RESISTANT IDIOPATHIC THROMBOCYTOPENIC PURPURA (ITP), American journal of hematology, 51(1), 1996, pp. 37-44
The efficacy of recombinant human interferon alpha-2b (rh IFN alpha-2b
) in the treatment of steroid resistant idiopathic thrombocytopenic pu
rpura (ITP) was studied in 50 cases. Forty-one patients treated with r
h IFN alpha-2b three times a week, six of 18 (33.3%) in the low dose g
roup (150 x 10(4)IU: 3 MIU) and four of 20 (20.0%) in the high dose gr
oup (300 x 10(4)IU: 3 MIU) responded with platelet counts increasing t
o above 50 x 10(9)/L, Because of the exacerbation of thrombocytopenia
and nasal bleeding, treatment was discontinued within 2 weeks in three
patients out of 41 cases, On the other hand, six of nine patients (66
.7%) treated with 3 MIU of IFN alpha-2b once a week for 8 weeks showed
satisfactory response.Treatment with either administration schedule d
id not result in sustaining platelet counts above 50 x 10(9)/1 for a l
ong time after treatment, The results indicate that once a week admini
stration schedule of rh IFN alpha-Pb is more efficacious for platelet
counts increasing for short period in patients who failed to respond t
o steroid and other medications than other schedules, The maintenance
of this treatment schedule will allow sustained increased platelet lev
els, resulting in relief of bleeding tendency, while also being cost e
ffective in comparison with other IFN treatment schedules and achievin
g better patient compliance without flu-like symptoms. (C) 1996 Wiley-
Liss, Inc.