TY - JOUR
T1 - Vitamin K Antagonists After 6 Months of Low-Molecular-Weight Heparin in Cancer Patients with Venous Thromboembolism
AU - Chai-Adisaksopha, Chatree
AU - Iorio, Alfonso
AU - Crowther, Mark A.
AU - de Miguel, Javier
AU - Salgado, Estuardo
AU - Zdraveska, Marija
AU - Fernández-Capitán, Carmen
AU - Nieto, José Antonio
AU - Barillari, Giovanni
AU - Bertoletti, Laurent
AU - Monreal, Manuel
AU - RIETE Investigators
A2 - Aibar, M. A.
A2 - Arcelus, J. I.
A2 - Ballaz, A.
A2 - Barba, R.
A2 - Barrón, M.
A2 - Barrón-Andrés, B.
A2 - Bascuñana, J.
A2 - Blanco-Molina, A.
A2 - Bueso, T.
A2 - Calvo, B.
A2 - Cañada, G.
A2 - Cañas, I.
A2 - Casado, I.
A2 - Culla, A.
A2 - del Toro, J.
A2 - Díaz-Peromingo, J. A.
A2 - Falgá, C.
A2 - Font, C.
A2 - Guil, M.
A2 - Gutiérrez, J.
A2 - Hernández, G.
A2 - Hernández-Blasco, L.
A2 - Isern, V.
A2 - Jara-Palomares, L.
A2 - Jaras, M. J.
A2 - Jiménez, D.
A2 - Lacruz, B.
A2 - Lecumberri, R.
A2 - Lobo, J. L.
A2 - López-Jiménez, L.
A2 - Drucka, E.
A2 - Kigitovica, D.
A2 - Skride, A.
N1 - Full list of the RIETE Investigators is given in Scopus, Pubmed, ScienceDirect publications.
Funding Information:
Conflicts of Interest: MAC discloses having sat on advisory boards for Janssen, Leo Pharma, Portola, and AKP America. MAC holds a Career Investigator award from the Heart and Stroke Foundation of Ontario, and the Leo Pharma Chair in Thromboembolism Research at McMaster University. MAC's institution has received funding for research projects from Leo Pharma. MAC has received funding for presentations from Leo Pharma, Bayer, Celgene, Shire and CSL Behring. MM discloses having sat on advisory boards for Leo Pharma, Bayer, and Sanofi. CC, AI, JM, ES, MZ, CFC, JAN, GB, and LB have no relevant conflicts of interest.
Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/4/1
Y1 - 2018/4/1
N2 - Background: Low-molecular-weight heparin (LMWH) is the treatment of choice in cancer patients with venous thromboembolism. However, data on continuing LMWH treatment beyond 6 months remain scanty. Methods: We used the RIETE (Registro Informatizado Enfermedad TromboEmbólica) registry to compare the rate of venous thromboembolism recurrences and major bleeding appearing beyond the first 6 months of anticoagulant therapy in cancer patients with venous thromboembolism, according to therapy with LMWH or vitamin K antagonists (VKA). We performed a propensity score-matched cohort study. Results: After propensity matching, 482 cancer patients continued to receive LMWH and 482 switched to VKA. During the course of anticoagulant therapy (mean 275.5 days), 57 patients developed venous thrombosis recurrences (recurrent pulmonary embolism 26, recurrent deep vein thrombosis 29, both 2), 28 had major bleeding, 38 had nonmajor bleeding, and 129 died. No patient died of recurrent venous thrombosis, and 5 patients died of bleeding (2 were on LMWH, 3 on VKA). Patients who continued with LMWH had a similar rate of deep vein thrombosis recurrences (relative risk [RR] 1.41; 95% confidence interval [CI], 0.68-2.93), pulmonary embolism recurrences (RR 0.73; 95% CI, 0.34-1.58), major bleeding (RR 0.96; 95% CI, 0.51-1.79), or nonmajor bleeding (RR 1.15; 95% CI, 0.55-2.40), compared with those who switched to VKA, but a higher mortality rate (RR 1.58; 95% CI, 1.13-2.20). Conclusions: In cancer patients with venous thromboembolism who completed 6 months of LMWH therapy, switching to VKA was associated with a similar risk of venous thrombosis recurrences or bleeding when compared with patients who continued LMWH.
AB - Background: Low-molecular-weight heparin (LMWH) is the treatment of choice in cancer patients with venous thromboembolism. However, data on continuing LMWH treatment beyond 6 months remain scanty. Methods: We used the RIETE (Registro Informatizado Enfermedad TromboEmbólica) registry to compare the rate of venous thromboembolism recurrences and major bleeding appearing beyond the first 6 months of anticoagulant therapy in cancer patients with venous thromboembolism, according to therapy with LMWH or vitamin K antagonists (VKA). We performed a propensity score-matched cohort study. Results: After propensity matching, 482 cancer patients continued to receive LMWH and 482 switched to VKA. During the course of anticoagulant therapy (mean 275.5 days), 57 patients developed venous thrombosis recurrences (recurrent pulmonary embolism 26, recurrent deep vein thrombosis 29, both 2), 28 had major bleeding, 38 had nonmajor bleeding, and 129 died. No patient died of recurrent venous thrombosis, and 5 patients died of bleeding (2 were on LMWH, 3 on VKA). Patients who continued with LMWH had a similar rate of deep vein thrombosis recurrences (relative risk [RR] 1.41; 95% confidence interval [CI], 0.68-2.93), pulmonary embolism recurrences (RR 0.73; 95% CI, 0.34-1.58), major bleeding (RR 0.96; 95% CI, 0.51-1.79), or nonmajor bleeding (RR 1.15; 95% CI, 0.55-2.40), compared with those who switched to VKA, but a higher mortality rate (RR 1.58; 95% CI, 1.13-2.20). Conclusions: In cancer patients with venous thromboembolism who completed 6 months of LMWH therapy, switching to VKA was associated with a similar risk of venous thrombosis recurrences or bleeding when compared with patients who continued LMWH.
KW - Anticoagulants
KW - Cancer
KW - Low-molecular-weight heparin
KW - Thromboembolism
KW - Warfarin
UR - http://www.scopus.com/inward/record.url?scp=85041106576&partnerID=8YFLogxK
UR - https://www.riete.org/info/centros_participantes/index.php
UR - https://www.sciencedirect.com/science/article/abs/pii/S0002934317312779
U2 - 10.1016/j.amjmed.2017.11.042
DO - 10.1016/j.amjmed.2017.11.042
M3 - Article
C2 - 29274307
AN - SCOPUS:85041106576
SN - 0002-9343
VL - 131
SP - 430
EP - 437
JO - American Journal of Medicine
JF - American Journal of Medicine
IS - 4
ER -