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1 ng agents, recombinant interferon alpha, and anagrelide.
2 ons for the monitoring of patients receiving anagrelide.
4 re was no significant difference between the anagrelide and hydroxyurea group regarding incidences of
5 erferon or pegylated interferon, pipobroman, anagrelide, approved immunomodulators, or no cytoreducti
7 ion system, the efficacy and tolerability of anagrelide compared with hydroxyurea were investigated i
10 oncluded that long-term treatment of ET with anagrelide is associated with decreased reporting of ini
12 n hemoglobin levels in patients treated with anagrelide (P < .0001), but not in those receiving hydro
13 thrombosis, in patients with ET treated with anagrelide plus aspirin compared to hydroxyurea plus asp
14 developed increased bone marrow reticulin on anagrelide showed regression of fibrosis when switched t
15 e specimens in patients randomly assigned to anagrelide showed significantly greater increases in ret
17 33 responding patients, 27 (82%) remained on anagrelide therapy for a median of 10.8 years (range, 7
18 These data suggest that patients receiving anagrelide therapy should undergo surveillance bone marr
21 Confirmatory proof of the noninferiority of anagrelide was achieved after 6 months using the primary
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