作者
Christoph Male,Anthonie W.A. Lensing,Joseph S. Palumbo,Riten Kumar,Ildar Nurmeev,Kerry Hege,Damien Bonnet,Philip Connor,Hélène L. Hooimeijer,Marcela Torres,Anthony Chan,Gili Kenet,Susanne Holzhauer,Amparo Santamaría,Pascal Amédro,Elizabeth Chalmers,Paolo Simioni,Rukhmi Bhat,Donald L. Yee,O. Lvova,Jan Beyer‐Westendorf,Tina Biss,Ida Martinelli,Paola Saracco,Marjolein Peters,Krisztián Kállay,Cynthia Gauger,M. Patricia Massicotte,Guy Young,Á Pap,Madhurima Majumder,William T. Smith,Jürgen F. Heubach,Scott D. Berkowitz,Kirstin Thelen,Dagmar Kubitza,Mark Crowther,Martin H. Prins,Paul Monagle,Angelo Claudio Molinari,Ulrike Nowak- Gottl,Juan José Chain,Jeremy Robertson,Katharina Thom,Werner Streif,Rudolf Schwarz,К. Schimrigk,Gernot Grangl,An Van Damme,Philip Maes,Veerle Labarque,Antônio Sérgio Petrilli,Sandra Loggeto,Estela Azeka,Leonardo R. Brandão,Doan Le,Christine Sabapathy,Paola Giordano,Ronghai Wu,Jie Ding,Wenyan Huang,Jianhua Mao,Päivi Lähteenmäki,Stéphane Decramer,Toralf Bernig,Martin Chada,Godfrey Chi‐Fung Chan,Krisztian Kally,Beatrice Nolan,Shoshana Revel‐Vilk,Hannah Tamary,Carina Levin,Daniela Tormene,Maria Abbattista,Andrea Artoni,Takanari Ikeyama,Ryo Inuzuka,Satoshi Yasukochi,Michelle Morales Soto,Karina Solis Labastida,Monique H. Suijker,Marike Bartels,R. Y. J. Tamminga,C. Heleen van Ommen,Dyani Loo,Rui Anjos,L. S. Zubarovskaya,Н. В. Попова,Elena Samochatova,М. Б. Белогурова,Pavel Svirin,Tatiana Shutova,В. В. Лебедев,О. Л. Барбараш,P. Koh,Joyce Mei,Ľudmila Podracká,Rubén Berrueco,María del Pilar Fernández,Tony Frisk,Sebastian Grunt,Johannes Rischewski,Manuela Albisetti-Pedroni,Ali Bülent Antmen,Hüseyin Tokgöz,Zeynep Karakaş,Muralidharan Jayashree,Michael G. Williams,John D. Grainger,Jeanette Payne,Mike Richards,Susan Baird,Neha Bhatnagar,Angela Aramburo,Shelley E. Crary,Tung Wynn,Shannon L. Carpenter,Sanjay P. Ahuja,Neil A. Goldenberg,Gary M. Woods,Kamar Godder,Ajovi B. Scott‐Emuakpor,Gavin D. Roach,Leslie Raffini,Nirmish Shah,Sanjay Shah,Courtney D. Thornburg,Ayesha Zia,Roger L. Berkow
摘要
Background Treatment of venous thromboembolism in children is based on data obtained in adults with little direct documentation of its efficacy and safety in children. The aim of our study was to compare the efficacy and safety of rivaroxaban versus standard anticoagulants in children with venous thromboembolism. Methods In a multicentre, parallel-group, open-label, randomised study, children (aged 0–17 years) attending 107 paediatric hospitals in 28 countries with documented acute venous thromboembolism who had started heparinisation were assigned (2:1) to bodyweight-adjusted rivaroxaban (tablets or suspension) in a 20-mg equivalent dose or standard anticoagulants (heparin or switched to vitamin K antagonist). Randomisation was stratified by age and venous thromboembolism site. The main treatment period was 3 months (1 month in children <2 years of age with catheter-related venous thromboembolism). The primary efficacy outcome, symptomatic recurrent venous thromboembolism (assessed by intention-to-treat), and the principal safety outcome, major or clinically relevant non-major bleeding (assessed in participants who received ≥1 dose), were centrally assessed by investigators who were unaware of treatment assignment. Repeat imaging was obtained at the end of the main treatment period and compared with baseline imaging tests. This trial is registered with ClinicalTrials.gov, number NCT02234843 and has been completed. Findings From Nov 14, 2014, to Sept 28, 2018, 500 (96%) of the 520 children screened for eligibility were enrolled. After a median follow-up of 91 days (IQR 87–95) in children who had a study treatment period of 3 months (n=463) and 31 days (IQR 29–35) in children who had a study treatment period of 1 month (n=37), symptomatic recurrent venous thromboembolism occurred in four (1%) of 335 children receiving rivaroxaban and five (3%) of 165 receiving standard anticoagulants (hazard ratio [HR] 0·40, 95% CI 0·11–1·41). Repeat imaging showed an improved effect of rivaroxaban on thrombotic burden as compared with standard anticoagulants (p=0·012). Major or clinically relevant non-major bleeding in participants who received ≥1 dose occurred in ten (3%) of 329 children (all non-major) receiving rivaroxaban and in three (2%) of 162 children (two major and one non-major) receiving standard anticoagulants (HR 1·58, 95% CI 0·51–6·27). Absolute and relative efficacy and safety estimates of rivaroxaban versus standard anticoagulation estimates were similar to those in rivaroxaban studies in adults. There were no treatment-related deaths. Interpretation In children with acute venous thromboembolism, treatment with rivaroxaban resulted in a similarly low recurrence risk and reduced thrombotic burden without increased bleeding, as compared with standard anticoagulants. Funding Bayer AG and Janssen Research & Development.