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Hydroxycarbamide plus Aspirin vs Aspirin alone in patients with essential Thrombocythaemia aged 40-59 years without high-risk features

Abstract:
Purpose: Cytoreductive therapy is beneficial in patients with essential thrombocythemia at high risk of thrombosis. However its value in those lacking high-risk features remains unknown. This open-label, randomized trial compared hydroxycarbamide plus aspirin with aspirin alone in patients with ET aged 40- 59 and without high-risk factors or extreme thrombocytosis. Methods: Patients were aged 40-59 years and lacked a history of ischemia, thrombosis, embolism, hemorrhage, extreme thrombocytosis (≥1500x109 /L), or hypertension or diabetes requiring therapy. 382 patients were randomized 1:1 to hydroxycarbamide plus aspirin or aspirin alone. The composite primary endpoint was time to arterial or venous thrombosis, serious hemorrhage or death from vascular causes. Secondary endpoints were time to first arterial or venous thrombosis, first serious hemorrhage, death, incidence of transformation and patient-reported quality of life. Results: After a median follow-up of 73 months and a total follow-up of 2373 patient years there was no significant difference between the arms in the likelihood of patients reaching the primary endpoint (hazard ratio 0.98, 95% CI 0.42-2.25, P=1.0). The incidence of significant vascular events was low, at 0.93 per 100 patient-years (95% CI 0.61-1.41). There were also no differences in overall 4 survival, in the composite endpoint of transformation to myelofibrosis, acute myeloid leukaemia or myelodysplasia, in adverse events or in patient-reported quality of life. Conclusions: In ET patients aged 40-59 and lacking high-risk factors for thrombosis or extreme thrombocytosis, pre-emptive addition of hydroxycarbamide to aspirin did not reduce vascular events, myelofibrotic or leukemic transformation. Patients aged 40-59 without other clinical indications for treatment (such as previous thrombosis or haemorrhage), who have a platelet count less than 1500x109 /L, should not receive cytoreductive therapy.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1200/JCO.2018.78.8414

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
Clinical Trial Service Unit
Role:
Author
ORCID:
0000-0001-5909-4265



Publisher:
American Society of Clinical Oncology
Journal:
Journal of Clinical Oncology More from this journal
Volume:
36
Issue:
34
Pages:
3361-3369
Publication date:
2018-08-28
Acceptance date:
2018-06-29
DOI:
EISSN:
1527-7755
ISSN:
0732-183X


Pubs id:
pubs:859742
UUID:
uuid:7965991e-66aa-47b4-8113-00aeb1d3dc87
Local pid:
pubs:859742
Source identifiers:
859742
Deposit date:
2018-06-29

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