Adverse effects and benefits of two years of anagrelide treatment for thrombocythemia in chronic myeloproliferative disorders

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Adverse effects and benefits of two years of anagrelide treatment for thrombocythemia in chronic myeloproliferative disorders. / Birgegard, G; Bjorkholm, M; Kutti, J; Larfars, G; Lofvenberg, E; Markevarn, B; Merup, M; Palmblad, J; Mauritzson, Nils; Westin, Jan; Samuelsson, J.

In: Haematologica, Vol. 89, No. 5, 2004, p. 520-527.

Research output: Contribution to journalArticle

Harvard

Birgegard, G, Bjorkholm, M, Kutti, J, Larfars, G, Lofvenberg, E, Markevarn, B, Merup, M, Palmblad, J, Mauritzson, N, Westin, J & Samuelsson, J 2004, 'Adverse effects and benefits of two years of anagrelide treatment for thrombocythemia in chronic myeloproliferative disorders', Haematologica, vol. 89, no. 5, pp. 520-527.

APA

Birgegard, G., Bjorkholm, M., Kutti, J., Larfars, G., Lofvenberg, E., Markevarn, B., ... Samuelsson, J. (2004). Adverse effects and benefits of two years of anagrelide treatment for thrombocythemia in chronic myeloproliferative disorders. Haematologica, 89(5), 520-527.

CBE

Birgegard G, Bjorkholm M, Kutti J, Larfars G, Lofvenberg E, Markevarn B, Merup M, Palmblad J, Mauritzson N, Westin J, Samuelsson J. 2004. Adverse effects and benefits of two years of anagrelide treatment for thrombocythemia in chronic myeloproliferative disorders. Haematologica. 89(5):520-527.

MLA

Vancouver

Birgegard G, Bjorkholm M, Kutti J, Larfars G, Lofvenberg E, Markevarn B et al. Adverse effects and benefits of two years of anagrelide treatment for thrombocythemia in chronic myeloproliferative disorders. Haematologica. 2004;89(5):520-527.

Author

Birgegard, G ; Bjorkholm, M ; Kutti, J ; Larfars, G ; Lofvenberg, E ; Markevarn, B ; Merup, M ; Palmblad, J ; Mauritzson, Nils ; Westin, Jan ; Samuelsson, J. / Adverse effects and benefits of two years of anagrelide treatment for thrombocythemia in chronic myeloproliferative disorders. In: Haematologica. 2004 ; Vol. 89, No. 5. pp. 520-527.

RIS

TY - JOUR

T1 - Adverse effects and benefits of two years of anagrelide treatment for thrombocythemia in chronic myeloproliferative disorders

AU - Birgegard, G

AU - Bjorkholm, M

AU - Kutti, J

AU - Larfars, G

AU - Lofvenberg, E

AU - Markevarn, B

AU - Merup, M

AU - Palmblad, J

AU - Mauritzson, Nils

AU - Westin, Jan

AU - Samuelsson, J

PY - 2004

Y1 - 2004

N2 - Background and Objectives. Although anagrelide is widely used in the treatment of throm-bocythemia in myeloproliferative diseases, there is currently limited information on the efficacy and toxicity of its long-term use. This prospective study investigated clinical toxicity and efficacy of anagrelide during two years of treatment. Design and Methods. A multicenter, open, phase II study of anagrelide treatment was performed by the Swedish Myeloproliferative Disorder Study Group. The study included 60 patients with thrombocythemia due to myeloproliferative disease, 42 with essential thrombocythemia (ET), 17 with polycythemia vera (PV) and one with myelofibrosis (MF). Results. Complete response (CR), defined as a platelet count <400x10(9)/L in symptomatic patients and < 600x10(9)/L in asymptomatic patients was achieved in 67% of the patients and partial response (PR) in 6%. The response rate was higher in patients with ET than in those with PV (p = 0.05). Primary treatment failure occurred in 27% due to lack of efficacy at a tolerable dose (n=13) or insufficient platelet response without side effects (n=3). In addition, another 14 patients withdrew from treatment before the end of the two-year period due to side effects. Side effects included palpitations (70%), headache (52%), nausea (35%), diarrhea or flatulence (33%), edema (22%) and fatigue (23%). Patients and doctors rated their satisfaction with the anagrelide treatment on a 10-grade scale from 7.6 at 3 months to >9 at 24 months. After two years, 50% (n=30) of the patients continued anagrelide treatment. Interpretation and Conclusions. Side effects and toxic discontinuation rates were higher than in previous studies, probably because this is the first long-term prospective study of the feasibility and toxicity of anagrelide treatment. Nevertheless, anagrelide is a valuable alternative for treatment of thrombocythemia in myeloproliferative disorders for patients who tolerate the drug well.

AB - Background and Objectives. Although anagrelide is widely used in the treatment of throm-bocythemia in myeloproliferative diseases, there is currently limited information on the efficacy and toxicity of its long-term use. This prospective study investigated clinical toxicity and efficacy of anagrelide during two years of treatment. Design and Methods. A multicenter, open, phase II study of anagrelide treatment was performed by the Swedish Myeloproliferative Disorder Study Group. The study included 60 patients with thrombocythemia due to myeloproliferative disease, 42 with essential thrombocythemia (ET), 17 with polycythemia vera (PV) and one with myelofibrosis (MF). Results. Complete response (CR), defined as a platelet count <400x10(9)/L in symptomatic patients and < 600x10(9)/L in asymptomatic patients was achieved in 67% of the patients and partial response (PR) in 6%. The response rate was higher in patients with ET than in those with PV (p = 0.05). Primary treatment failure occurred in 27% due to lack of efficacy at a tolerable dose (n=13) or insufficient platelet response without side effects (n=3). In addition, another 14 patients withdrew from treatment before the end of the two-year period due to side effects. Side effects included palpitations (70%), headache (52%), nausea (35%), diarrhea or flatulence (33%), edema (22%) and fatigue (23%). Patients and doctors rated their satisfaction with the anagrelide treatment on a 10-grade scale from 7.6 at 3 months to >9 at 24 months. After two years, 50% (n=30) of the patients continued anagrelide treatment. Interpretation and Conclusions. Side effects and toxic discontinuation rates were higher than in previous studies, probably because this is the first long-term prospective study of the feasibility and toxicity of anagrelide treatment. Nevertheless, anagrelide is a valuable alternative for treatment of thrombocythemia in myeloproliferative disorders for patients who tolerate the drug well.

KW - thrombocythemia

KW - anagrelide

KW - myeloproliferative disease

M3 - Article

VL - 89

SP - 520

EP - 527

JO - Haematologica-The Hematology Journal

T2 - Haematologica-The Hematology Journal

JF - Haematologica-The Hematology Journal

SN - 1592-8721

IS - 5

ER -