Designs of the included studies
| . | EXCLAIM 2010 . | MAGELLAN 2013 . | APEX 2016 . | MARINER 2018 . |
|---|---|---|---|---|
| Authors | Hull et al15 | Cohen et al14 | Cohen et al16 | Spyropoulos et al13 |
| Year of publication | 2010 | 2013 | 2016 | 2018 |
| Setting | International, multicenter | International, multicenter | International, multicenter | International, multicenter |
| Study design | Randomized parallel placebo-controlled trial | Randomized active comparator–controlled trial | Randomized active comparator–controlled trial | Randomized placebo-controlled trial |
| Blinding | Double blind | Double blind | Double blind, double dummy | Double blind |
| Cancer status | Active cancer or history of cancer | History of cancer or active cancer | History of cancer or active cancer | History of cancer in the past 5 y |
| Excludes intracranial neoplasm or metastasis | Excludes intracranial neoplasm or metastasis | Excludes intracranial neoplasm or metastasis, active lung cancer with residual disease, and nonmelanoma skin cancer | Excludes all active cancers and nonmelanoma skin cancer | |
| Intervention | 40 mg enoxaparin SC daily for 10 ± 4 d then enoxaparin 40 mg SC daily for additional 28 ± 4 d | 10 mg rivaroxaban daily for 35 ± 4 d | 80 mg betrixaban orally daily for 35-42 d (loading dose, 160 mg); reduced-dose betrixaban (40 mg) for patients with severe renal insufficiency or receiving concomitant P-glycoprotein inhibitor | 10 mg rivaroxaban daily for 45 d after discharge |
| Control | 40 mg enoxaparin SC daily for 10 ± 4 d then placebo for additional 28 ± 4 d | 40 mg enoxaparin SC daily for 10 ± 4 d | 40 mg enoxaparin SC daily for 10 ± 4 d | Placebo for 45 d after discharge |
| . | EXCLAIM 2010 . | MAGELLAN 2013 . | APEX 2016 . | MARINER 2018 . |
|---|---|---|---|---|
| Authors | Hull et al15 | Cohen et al14 | Cohen et al16 | Spyropoulos et al13 |
| Year of publication | 2010 | 2013 | 2016 | 2018 |
| Setting | International, multicenter | International, multicenter | International, multicenter | International, multicenter |
| Study design | Randomized parallel placebo-controlled trial | Randomized active comparator–controlled trial | Randomized active comparator–controlled trial | Randomized placebo-controlled trial |
| Blinding | Double blind | Double blind | Double blind, double dummy | Double blind |
| Cancer status | Active cancer or history of cancer | History of cancer or active cancer | History of cancer or active cancer | History of cancer in the past 5 y |
| Excludes intracranial neoplasm or metastasis | Excludes intracranial neoplasm or metastasis | Excludes intracranial neoplasm or metastasis, active lung cancer with residual disease, and nonmelanoma skin cancer | Excludes all active cancers and nonmelanoma skin cancer | |
| Intervention | 40 mg enoxaparin SC daily for 10 ± 4 d then enoxaparin 40 mg SC daily for additional 28 ± 4 d | 10 mg rivaroxaban daily for 35 ± 4 d | 80 mg betrixaban orally daily for 35-42 d (loading dose, 160 mg); reduced-dose betrixaban (40 mg) for patients with severe renal insufficiency or receiving concomitant P-glycoprotein inhibitor | 10 mg rivaroxaban daily for 45 d after discharge |
| Control | 40 mg enoxaparin SC daily for 10 ± 4 d then placebo for additional 28 ± 4 d | 40 mg enoxaparin SC daily for 10 ± 4 d | 40 mg enoxaparin SC daily for 10 ± 4 d | Placebo for 45 d after discharge |
SC, subcutaneous.