共 50 条
The Efficacy and Safety of Rivaroxaban and Dalteparin in the Treatment of Cancer Associated Venous Thrombosis
被引:37
|作者:
Chaudhury, Ateefa
[1
,2
]
Balakrishnan, Asha
[3
]
Thai, Christy
[4
]
Holmstrom, Bjorn
[5
]
Nanjappa, Sowmya
[5
]
Ma, Zhenjun
[6
]
Jaglal, Michael, V
[1
,2
,3
]
机构:
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Malignant Hematol, 12902 Magnolia Dr, Tampa, FL 33612 USA
[2] Univ S Florida, Dept Internal Med, Div Hematol & Med Oncol, Tampa, FL 33620 USA
[3] H Lee Moffitt Canc Ctr & Res Inst, Dept Internal Hosp Med, Tampa, FL 33612 USA
[4] H Lee Moffitt Canc Ctr & Res Inst, Dept Pharm, Tampa, FL USA
[5] H Lee Moffitt Canc Ctr & Res Inst, Dept Internal Hosp Med, Tampa, FL USA
[6] H Lee Moffitt Canc Ctr & Res Inst, Dept Biostat & Bioinformat, Tampa, FL USA
关键词:
Venous thrombosis;
Cancer associated thrombosis;
Venous thromboembolism;
Thrombosis;
Novel anticoagulants;
MOLECULAR-WEIGHT HEPARIN;
THROMBOEMBOLISM;
D O I:
10.1007/s12288-017-0895-8
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Venous thromboembolism (VTE) is a complication of malignancy that is associated with significant mortality. The CLOT trial showed superiority of dalteparin in comparison to warfarin in preventing VTE recurrence. Rivaroxaban has been approved for treatment of deep venous thrombosis (DVT) and pulmonary embolism (PE). In the absence of large randomized trials in the oncology population, the efficacy and safety of rivaroxaban for the treatment of VTE in cancer patients needs to be assessed. A single-center retrospective chart review was conducted to assess the efficacy and safety of rivaroxaban compared with dalteparin in cancer-associated thrombosis. Out of 671 patients identified, 286 patients (107 in the rivaroxaban group and 179 in the dalteparin group) were eligible for analysis. The rivaroxaban group had a rate of VTE recurrence at 6 months of 4.9 versus 11.1% with dalteparin (p = 0.252). The incidence of recurrent DVT at 6 months was lower in patients treated with rivaroxaban (0%) compared with dalteparin (8.2%) at 6 months (p = 0.025). Incidence of recurrent PE in the rivaroxaban group (5%) versus dalteparin group (3.1%) at 6 months was not statistically significant (p = 0.675). No significant difference was identified between the rivaroxaban group and dalteparin group in the rate of major bleeding (2.8 vs. 1.1%, respectively). Rivaroxaban was comparable to dalteparin in prevention of VTE recurrence while having no significant differences with major or minor bleeding.
引用
收藏
页码:530 / 534
页数:5
相关论文