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1602 A Study of the Role of Antiplatelet Therapy in the Prevention of Thrombosis in Patients with Calr-Mutated Low Risk Essential ThrombocythemiaClinically Relevant Abstract

Myeloproliferative Syndromes: Clinical
Program: Oral and Poster Abstracts
Session: 634. Myeloproliferative Syndromes: Clinical: Poster I
Saturday, December 5, 2015, 5:30 PM-7:30 PM
Hall A, Level 2 (Orange County Convention Center)

Alberto Alvarez-Larrán1*, Paola Guglielmelli, PhD MD2*, Eduardo Arellano-Rodrigo3*, Martin Griesshammer, MD4*, Chiara Paoli5*, Ana Kerguelen6*, Francisca Ferrer-Marin7*, Juan Carlos Hernández-Boluda8*, Bjorn Andreasson, MD PhD9*, Jiri Schwarz10*, Valentín García-Gutierrez11*, Rosa M. Ayala, MD, PhD12, Pere Barba, M.D.13*, María Teresa Gómez-Casares14*, Radek C. Skoda, MD15, Carmen Burgaleta16*, Stefanie Slot17*, Jan Samuelsson, MD, PhD18, Alimam Samah19*, Yan Beauverd20*, Claire N. Harrison21, Francisco Cervantes22, Alessandro M. Vannucchi23 and Carlos Besses24

1Hematology Department, Hospital de Mar, Barcelona, Spain
2CRIMM-Centro Ricerca e Innovazione delle Malattie Mieloproliferative,Department of Experimental and Clinical Medicine, Azienda Ospedaliera-Universitaria Careggi, University of Florence, Florence, Italy
3Hemotherapy and Hemostasis Department, Hospital Clínic, Barcelona, Spain
4Department of Hematology and Oncology, Johannes-Wesling Clinic Minden, Minden, Germany
5CRIMM-Centro Ricerca e Innovazione delle Malattie Mieloproliferative and Department of Experimental and Clinical Medicine, Azienda Ospedaliero-Universitaria Careggi, University of Florence, Florence, Italy
6Hematology Department, Hospital La Paz, Madrid, Spain
7Hematology Department, h, Murcia, Spain
8Hematology Department, Hospital Clínico, Valencia, Spain
9NU Hospital Organization, Uddavella, Sweden
10Leukemia PCR Diagnostics Laboratory, Institute of Hematology and Blood Transfusion, Prague, Czech Republic
11Hematology Department, Hospital Ramón y Cajal, Madrid, Spain
12Hematology Department, Hospital 12 de Octubre, Madrid, Spain
13Hospital Universitario Valld'Hebron, Barcelona, Spain
14Hematology Department, Hospital Dr Negrín, Las Palmas de Gran Canaria, Spain
15Department of Biomedicine, Experimental Hematology, University Hospital Basel, Basel, Switzerland
16Hospital Universitario Príncipe de Asturias, Alcalá de Henares, Spain
17Hematology Department, VU University Medical Center, Amsterdam, Netherlands
18Department of Internal Medicin, Section of Hematology, Stockholm South Hospital, Stockholm, Sweden
19Guys' and St Thomas' Hospital, London, United Kingdom
20Hematology Department, Guys' and St Thomas' Hospital, London, United Kingdom
21Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
22Hospital Clinic, IDIBAPS, University of Barcelona, Barcelona, Spain
23CRIMM-Centro Ricerca e Innovazione delle Malattie Mieloproliferative, Azienda Ospedaliera-Universitaria Careggi, Florence, Italy
24Hematology Department, Hospital del Mar, Barcelona, Spain

Young patients (age < 60 years) with essential thrombocythemia (ET) and no history of thrombosis are considered at low risk of thrombosis and therefore managed on a conservative approach with antiplatelet therapy or even without any treatment.  JAK2V617F and CALR exon 9 mutations are the most frequent molecular alterations observed in ET, with CALR-positive ET being considered a distinct clinical entity due to its higher platelet counts and lower incidence of thrombosis as compared with JAK2V617F-positive ET. There is some evidence supporting a role for antiplatelet therapy in JAK2V7617F-positive neoplasms. However, the role of antiplatelet therapy in CALR-positive ET has not been studied.

The aim of the present study was to assess the effect of antiplatelet therapy in the primary prevention of thrombosis in patients with CALR-positive ET without indication of cytoreductive therapy. For such purpose, 240 patients (107 males, 133 females) diagnosed with ET at a median age of 42 years (range 13-59) were included in a multicenter retrospective study. Initial treatment consisted of antiplatelet therapy (n=109) or careful observation (n=108), whereas 23 patients received cytoreduction since diagnosis and were excluded. During a median follow up of 8 years, 137 patients were started on cytoreductive therapy because of the following indications: age > 60 years (n=10), thrombosis (n=10), bleeding (n=2), microvascular symptoms (n=18), extreme thrombocytosis (n=89), and others (n=8). Median time free of cytoreductive therapy was 3.2 years. Thrombosis-free survival restricted to the time of cytoreductive therapy abstention was calculated using the Kaplan-Meier method. Variables attaining a significant level at the univariate analysis were included in a Cox proportional hazard model.

During the period of abstention of cytoreductive therapy, a total of 10 thrombotic events and 8 major bleeding episodes were registered. The probability of thrombosis at 3 years was 5% in patients managed with careful observation and 1% in those receiving antiplatelet therapy (p = 0.2). At multivariate analysis, antiplatelet therapy did not result in a lower risk of thrombosis after correction for age, sex and presence of cardiovascular risk factors. Interaction studies did not identify any subgroup of patients that benefited from antiplatelet therapy in thrombosis prevention. Regarding major bleeding, patients receiving antiplatelet therapy experienced a higher rate than those managed on observation (3-year probability of major bleeding, 5.5% and 0%, respectively, p=0.05). At multivariate analysis, antiplatelet therapy was associated with a tendency towards and increased risk of major bleeding (HR: 7.7, 95%CI: 0.9-66.2, p=0.06) independently of platelet count at diagnosis, age and gender.  

In conclusion, CALR-mutated low-risk ET patients under cytoreductive therapy abstention may not obtain a clear benefit from antiplatelet therapy since the increase in the rate of bleeding may offset the reduction in the rate of thrombosis

Disclosures: García-Gutierrez: Pfizer: Consultancy , Membership on an entity’s Board of Directors or advisory committees , Research Funding ; BMS: Consultancy , Membership on an entity’s Board of Directors or advisory committees , Research Funding ; Ariad: Consultancy , Membership on an entity’s Board of Directors or advisory committees , Research Funding ; Novartis: Consultancy , Membership on an entity’s Board of Directors or advisory committees , Research Funding . Harrison: Sanofi: Honoraria , Speakers Bureau ; Gilead: Honoraria ; Shire: Speakers Bureau ; CTI Biopharma: Consultancy , Honoraria , Speakers Bureau ; Novartis: Honoraria , Research Funding , Speakers Bureau . Cervantes: Sanofi-Aventis: Consultancy ; Novartis: Consultancy , Speakers Bureau ; CTI-Baxter: Consultancy , Speakers Bureau . Vannucchi: Shire: Speakers Bureau ; Baxalta: Membership on an entity’s Board of Directors or advisory committees ; Novartis Pharmaceuticals Corporation: Membership on an entity’s Board of Directors or advisory committees , Research Funding , Speakers Bureau .

*signifies non-member of ASH