Please use this identifier to cite or link to this item:
http://elar.urfu.ru/handle/10995/131435
Title: | Dabigatran in the treatment and secondary prophylaxis of venous thromboembolism in children with thrombophilia |
Authors: | Brandão, L. R. Tartakovsky, I. Albisetti, M. Halton, J. Bomgaars, L. Chalmers, E. Luciani, M. Saracco, P. Felgenhauer, J. Lvova, O. Simetzberger, M. Sun, Z. Mitchell, L. G. |
Issue Date: | 2022 |
Publisher: | American Society of Hematology |
Citation: | Brandão, LR, Tartakovsky, I, Albisetti, M, Halton, J, Bomgaars, L, Chalmers, E, Luciani, M, Saracco, P, Felgenhauer, J, Lvova, O, Simetzberger, M, Sun, Z & Mitchell, LG 2022, 'Dabigatran in the treatment and secondary prophylaxis of venous thromboembolism in children with thrombophilia', Blood Advances, Том. 6, № 22, стр. 5908-5923. https://doi.org/10.1182/bloodadvances.2021005681 Brandão, L. R., Tartakovsky, I., Albisetti, M., Halton, J., Bomgaars, L., Chalmers, E., Luciani, M., Saracco, P., Felgenhauer, J., Lvova, O., Simetzberger, M., Sun, Z., & Mitchell, L. G. (2022). Dabigatran in the treatment and secondary prophylaxis of venous thromboembolism in children with thrombophilia. Blood Advances, 6(22), 5908-5923. https://doi.org/10.1182/bloodadvances.2021005681 |
Abstract: | In the phase 2b/3 DIVERSITY trial, 3 months treatment with dabigatran was noninferior to standard of care (SOC) for acute venous thromboembolism (VTE) in children. In a single-arm, phase 3, secondary VTE prevention study, up to 12 months dabigatran use was associated with favorable safety. Dabigatran is approved by the European Medicines Agency and US Food and Drug Administration for pediatric indications. We assessed primary composite efficacy (complete thrombus resolution and freedom from VTE recurrence/VTE-related death) in subgroups with thrombophilia vs those with negative/unknown thrombophilia status in the DIVERSITY trial and safety in both studies. Thrombophilia types were similar between the DIVERSITY trial (total population) and secondary prevention studies: factor V Leiden, 42% vs 33%; prothrombin mutation (G20210A), 19% vs 17%; antithrombin deficiency, 15% vs 20%; protein C/S deficiency, 23% vs 25%; and antiphospholipid antibodies, 18% vs 20% of patients, respectively. In DIVERSITY, 36% and 22% of thrombophilia subgroup patients treated with dabigatran and SOC, respectively, met the primary end point (Mantel-Haenszel–weighted rate difference, -0.135; 95% confidence interval, -0.36 to 0.08; noninferiority P = .0014); comparable to the total DIVERSITY trial population (46% vs 42%) showing dabigatran noninferiority to SOC. Within this subgroup, numerically fewer patients experienced VTE recurrence or progression of index thrombus in the dabigatran treatment group vs SOC. In the secondary prevention study, VTE recurrence at 12 months occurred in 2.8% of patients with thrombophilia vs 0% with negative/unknown thrombophilia. Safety profiles were consistent with those reported previously. Although they should be interpreted with caution, these exploratory findings suggest dabigatran could be an appropriate long-term anticoagulant for children with thrombophilia. © 2022 by The American Society of Hematology. |
Keywords: | BLOOD CLOTTING FACTOR 5 LEIDEN DABIGATRAN PHOSPHOLIPID ANTIBODY PROTHROMBIN PROTHROMBIN ANTIBODY ADVERSE OUTCOME ALOPECIA ARTICLE CHILD CLINICAL EFFECTIVENESS CLINICAL FEATURE DISEASE EXACERBATION DRUG EFFECT DRUG EFFICACY DRUG RESPONSE DRUG SAFETY EPISTAXIS FEMALE HEADACHE HUMAN MAJOR CLINICAL STUDY MALE PHASE 3 CLINICAL TRIAL RECURRENT DISEASE RHINOPHARYNGITIS RISK FACTOR THROMBOPHILIA THROMBOSIS PREVENTION TREATMENT OUTCOME VENOUS THROMBOEMBOLISM |
URI: | http://elar.urfu.ru/handle/10995/131435 |
Access: | info:eu-repo/semantics/openAccess cc-by-nc-nd |
License text: | https://creativecommons.org/licenses/by-nc-nd/4.0/ |
SCOPUS ID: | 85143118299 |
WOS ID: | 000913702900015 |
PURE ID: | 32801602 f16b190c-a372-42f1-bd92-889793178d35 |
ISSN: | 2473-9529 |
DOI: | 10.1182/bloodadvances.2021005681 |
metadata.dc.description.sponsorship: | Boehringer Ingelheim The study was supported financially by Boehringer Ingelheim International GmbH. |
Appears in Collections: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
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