Long-term follow-up of 386 consecutive patients with essential thrombocythemia: safety of cytoreductive therapy

被引:60
作者
Palandri, Francesca [1 ]
Catani, Lucia [1 ]
Testoni, Nicoletta [1 ]
Ottaviani, Emanuela [1 ]
Polverelli, Nicola [1 ]
Fiacchini, Mauro [1 ]
De Vivo, Antonio [1 ]
Salmi, Federica [1 ]
Lucchesi, Alessandro [1 ]
Baccarani, Michele [1 ]
Vianelli, Nicola [1 ]
机构
[1] Univ Bologna, St Orsola Malpighi Hosp, Inst Hematol & Med Oncol L & A Seragnoli, Dept Hematol & Med Oncol L & A Seragnoli, I-40138 Bologna, Italy
关键词
ACUTE MYELOID-LEUKEMIA; POLYCYTHEMIA-VERA; RISK-FACTORS; DIAGNOSTIC-CRITERIA; HYDROXYUREA; THROMBOSIS; LEUKOCYTOSIS; SURVIVAL; PIPOBROMAN; CLASSIFICATION;
D O I
10.1002/ajh.21360
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cytotoxic agents like Hydroxyurea, Busulfan and Interferon-alpha are to date the most commonly used therapeutic approaches in Essential Thrombocythemia (ET). However, few data on the efficacy and safety of these agents in the long-term are currently available. We report a retrospective analysis of the long-term outcome of 386 consecutive ET patients, followed at single Institution for a median follow-up of 9.5 years (range, 3-28.5). Cytoreductive therapy was administered to 338 patients (88%), obtaining a response in 86% of cases. Forty-five patients (12%) experienced a thrombosis. Among baseline characteristics, only history of vascular events prior to ET diagnosis predicted a higher incidence of thrombosis. Evolution in acute leukemia/myelofibrosis occurred in 6 (1,5%) and 20 (5%) patients, and was significantly higher in patients receiving sequential cytotoxic agents. Overall survival was 38% at 19 years and was poorer for patients older than 60 years, with higher leukocytes count (>15 x 10(9)/L), hypertension and mellitus diabetes at ET diagnosis and for patients experiencing a thrombotic event during follow-up. Cytoreductive therapy was effective in decreasing platelet number with negligible toxicity; however, thrombocytosis control did not reduce the incidence of thrombosis and, for patients who received sequential therapies, the probability of disease evolution was higher and survival was poorer. Am. J. Hematol. 84:215-220, 2009. (C) 2008 Wiley-Liss, Inc.
引用
收藏
页码:215 / 220
页数:6
相关论文
共 32 条
[1]   Leukemic transformation of essential thrombocythemia without previous cytoreductive treatment [J].
Andersson, PO ;
Ridell, B ;
Wadenvik, H ;
Kutti, J .
ANNALS OF HEMATOLOGY, 2000, 79 (01) :40-42
[2]  
Barbui T, 2004, HAEMATOLOGICA, V89, P215
[3]   The Italian consensus conference on diagnostic criteria for myelofibrosis with myeloid metaplasia [J].
Barosi, G ;
Ambrosetti, A ;
Finelli, C ;
Grossi, A ;
Leoni, P ;
Liberato, NL ;
Petti, MC ;
Pogliani, E ;
Ricetti, M ;
Rupoli, S ;
Visani, G ;
Tura, S .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 104 (04) :730-737
[4]   A unified definition of clinical resistance/intolerance to hydroxyurea in essential thrombocythemia: results of a consensus process by an international working group [J].
Barosi, G. ;
Besses, C. ;
Birgegard, G. ;
Briere, J. ;
Cervantes, F. ;
Finazzi, G. ;
Gisslinger, H. ;
Griesshammer, M. ;
Gugliotta, L. ;
Harrison, C. ;
Hasselbalch, H. ;
Lengfelder, E. ;
Reilly, J. T. ;
Michiels, J. J. ;
Barbui, T. .
LEUKEMIA, 2007, 21 (02) :277-280
[5]   Thrombosis-free survival and life expectancy in 187 consecutive patients with essential thrombocythemia [J].
Bazzan, M ;
Tamponi, G ;
Schinco, P ;
Vaccarino, A ;
Foli, C ;
Gallone, G ;
Pileri, A .
ANNALS OF HEMATOLOGY, 1999, 78 (12) :539-543
[6]   PROPOSALS FOR THE CLASSIFICATION OF THE MYELODYSPLASTIC SYNDROMES [J].
BENNETT, JM ;
CATOVSKY, D ;
DANIEL, MT ;
FLANDRIN, G ;
GALTON, DAG ;
GRALNICK, HR ;
SULTAN, C .
BRITISH JOURNAL OF HAEMATOLOGY, 1982, 51 (02) :189-199
[7]   PROPOSED REVISED CRITERIA FOR THE CLASSIFICATION OF ACUTE MYELOID-LEUKEMIA - A REPORT OF THE FRENCH-AMERICAN-BRITISH COOPERATIVE GROUP [J].
BENNETT, JM ;
CATOVSKY, D ;
DANIEL, MT ;
FLANDRIN, G ;
GALTON, DAG ;
GRALNICK, HR ;
SULTAN, C .
ANNALS OF INTERNAL MEDICINE, 1985, 103 (04) :620-625
[8]   Acute myeloid leukemia (AML) having evolved from essential thrombocythemia (ET): distinctive chromosome abnormalities in patients treated with pipobroman or hydroxyurea [J].
Bernasconi, P ;
Boni, M ;
Cavigliano, PM ;
Calatroni, S ;
Brusamolino, E ;
Passamonti, F ;
Volpe, G ;
Pistorio, A ;
Giardini, I ;
Rocca, B ;
Caresana, M ;
Lazzarino, M ;
Bernasconi, C .
LEUKEMIA, 2002, 16 (10) :2078-2083
[9]   Leukocytosis is a risk factor for thrombosis in essential thrombocythemia: interaction with treatment, standard risk factors, and Jak2 mutation status [J].
Carobbio, Alessandra ;
Finazzi, Guido ;
Guerini, Vittoria ;
Spinelli, Orietta ;
Delaini, Federica ;
Marchioli, Roberto ;
Borrelli, Giovanna ;
Rambaldi, Alessandro ;
Barbui, Tiziano .
BLOOD, 2007, 109 (06) :2310-2313
[10]   Myelofibrosis with myeloid metaplasia following essential thrombocythaemia:: actuarial probability, presenting characteristics and evolution in a series of 195 patients [J].
Cervantes, F ;
Alvarez-Larrán, A ;
Talarn, C ;
Gómez, M ;
Montserrat, E .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 118 (03) :786-790