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. 2023 Jun 6;25(9):979–987. doi: 10.1007/s11912-023-01428-y

Table 1.

Randomized controlled trials of anticoagulant therapy for cancer-associated venous thromboembolism

Study

(Ref. #)

Duration Tested LMWH Recurrent VTE Major bleeding
LMWH VKA LMWH VKA

CLOT

(8)

6 months Dalteparin 27/336 (8%) 53/336 (15.8%)* 19/338 (5.6%) 12/335 (3.6%)

CATCH

(9)

6 months Tinzaparin 31/449 (6.9%) 45/451 (10%) 12/449 (2.7%) 11/451 (2.4%)

CANTHANOX

(10)

3 months Enoxaparin 2/71 (2.8%)

3/75

(4%)

5/71

(7%)

12/75 (16%)

ONCENOX

(11)

6 months Enoxaparin 4/61 (6.6%)

3/30

(10%)

6/67 (8.9%) 1/34 (2.9%)

LITE

(12)

3 months Tinzaparin 18/369 (4.9%) 21/368 (5.7%) 10/144 (6.9%)

13/146

(8.9%)

Study

(Ref. #)

Duration Tested DOAC Recurrent VTE Major bleeding
DOAC dalteparin DOAC dalteparin

SELECT-D

(29)

6 months Rivaroxaban 8/203 (3.9%) 18/203 (8.9%)* 11/203 (5.4%)

6/203

(3%)

Hokusai VTE Cancer

(30)

Up to 9 months Edoxaban 41/522 (7.9%) 59/524 (11.3%) 36/522 (6.9%) 21/524 (4%)*

ADAM VTE

(31)

6 months Apixaban

0/145

(0%)

2/142 (1.4%) 1/145 (0.7%) 9/142 (6.3%)

Caravaggio

(32)

6 months Apixaban 32/576 (5.6%) 46/579 (7.9%) 22/576 (3.8%) 23/579 (4%)

The upper part of the table shows the frequency of recurrent venous thromboembolism (VTE) and major bleeding in randomized controlled trials comparing different types of low-molecular-weight heparin (LMWH) with vitamin K antagonists (VKA), while the lower part presents the same outcomes in trials evaluating direct oral anticoagulants (DOAC) vs. dalteparin. Event rates are expressed as total number divided by treated patients, as published

*Indicates significant difference for the corresponding hazard ratio