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Table 3 Comparison of trials on LMWH versus VKA for treatment of VTE in cancer patients

From: Management of venous thromboembolism: an update

Trial Name

CANTHANOX

CLOT

MAIN-LITE

ONCENOX

CATCH

Year of Publication [Ref]

2002 [43]

2003 [44]

2006 [45]

2006 [46]

2015 [47]

Design

Open-label

Open-label

Open-label

Open-label

Open-label

Number of Patients

146

676

200

122

900

Treatment Protocol

Enoxaparin 1.5 mg/kg daily

Dalteparin 200 IU/kg once daily for the first month then 150 IU/kg for 5 months

Tinzaparin 175 IU/kg once daily

Enoxaparin 1 mg/kg every 12 h for 5 days then enoxaparin 1 mg/kg or 1.5 mg/kg daily

Tinzaparin 175 IU/kg once daily

Duration of Therapy (months)

3

6

3

6

6

Primary Efficacy Outcome LMWH vs VKA (%)

Combination of major bleeding or recurrent VTE: 10.5 vs 21.1

Recurrent symptomatic VTE: 9a vs 17

Recurrent symptomatic VTE: 7 vs 10

Recurrent symptomatic VTE: enoxaparin 1 mg vs. 1.5 mg vs VKA 6.8 vs 6.3 vs 10.0

Composite of recurrent symptomatic VTE, fatal PE, or incidental VTE: 7.2 vs 10.5

Safety Bleeding Outcomes LMWH vs VKA (%)

Major bleeding: 7 vs 16;

Fatal bleeding: 0 vs 8a

Major bleeding: 6 vs 4;

Any bleeding 14 vs 19

Major bleeding: 7 vs 7;

Any bleeding: 27 vs 24

Major bleeding: enoxaparin 1 mg vs. 1.5 mg vs VKA : 6.5 vs 11.1 vs 2.9

Major bleeding: 2.7 vs 2.4 CRNM bleeding: 10.9a vs 15.3

  1. CRNM clinically relevant non-major, DOAC direct oral anticoagulants, LMWH low-molecular weight heparin, PE pulmonary embolism, VKA vitamin K antagonists, VTE venous thromboembolism
  2. aStatistically significant difference between the two groups