TY - JOUR
T1 - Direct oral anticoagulants for cancer-associated venous thromboembolism
T2 - a systematic review and meta-analysis
AU - Mulder, Frits I.
AU - Bosch, Floris T.M.
AU - Young, Annie M.
AU - Marshall, Andrea
AU - McBane, Robert D.
AU - Zemla, Tyler J.
AU - Carrier, Marc
AU - Kamphuisen, Pieter Willem
AU - Bossuyt, Patrick M.M.
AU - Büller, Harry R.
AU - Weitz, Jeffrey I.
AU - Middeldorp, Saskia
AU - van Es, Nick
N1 - Funding Information:
A.M.Y. received research funding from Bayer; and honoraria from Bayer, BMS/Pfizer Alliance, and Leo Pharma. A.M. received research funding from Bayer. M.C. received research funding from LEO Pharma, Bristol-Myers Squibb, and Pfizer; and advisory board honoraria from Bayer, Bristol-Myers Squibb, LEO Pharma, Pfizer, Servier, and Sanofi. P.W.K. received research funding from Daiichi Sankyo and Roche Diagnostics. J.I.W. declares consultancy and receipt of honoraria from Anthos, Bayer AG, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, Ionis, Janssen, Merck, Novartis, Pfizer, PhaseBio, Portola, Servier, and Tetherex Pharmaceuticals; and institutional grants from Bayer AG and Boehringer Ingelheim. S.M. received grants and fees paid to her institution from GlaxoSmithKline, BMS/Pfizer, Aspen, Daiichi Sankyo, Bayer, Boehringer Ingelheim, Sanofi, and Portola. N.v.E. reports advisory board honoraria from Daiichi-Sankyo, LEO Pharma, and Bayer. The remaining authors declare no competing financial interests.
Funding Information:
Conflict-of-interest disclosure: A.M.Y. received research funding from Bayer; and honoraria from Bayer, BMS/Pfizer Alliance, and Leo Pharma. A.M. received research funding from Bayer. M.C. received research funding from LEO Pharma, Bristol-Myers Squibb, and Pfizer; and advisory board honoraria from Bayer, Bristol-Myers Squibb, LEO Pharma, Pfizer, Servier, and Sanofi. P.W.K. received research funding from Daiichi Sankyo and Roche Diagnostics. J.I.W. declares consultancy and receipt of honoraria from Anthos, Bayer AG, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, Ionis, Janssen, Merck, Novartis, Pfizer, PhaseBio, Portola, Servier, and Tetherex Pharmaceuticals; and institutional grants from Bayer AG and Boehringer Ingelheim. S.M. received grants and fees paid to her institution from GlaxoSmithKline, BMS/Pfizer, Aspen, Daiichi Sankyo, Bayer, Boehringer Ingelheim, Sanofi, and Portola. N.v.E. reports advisory board honoraria from Daiichi-Sankyo, LEO Pharma, and Bayer. The remaining authors declare no competing financial interests.
Publisher Copyright:
© 2020 American Society of Hematology. All rights reserved.
PY - 2020/9/17
Y1 - 2020/9/17
N2 - Direct oral anticoagulants (DOACs) are an emerging treatment option for patients with cancer and acute venous thromboembolism (VTE), but studies have reported inconsistent results. This systematic review and meta-analysis compared the efficacy and safety of DOACs and low-molecular-weight heparins (LMWHs) in these patients. MEDLINE, Embase, the Cochrane Central Register of Controlled Trials, and conference proceedings were searched to identify relevant randomized controlled trials. Additional data were obtained from the original authors to homogenize definitions for all study outcomes. The primary efficacy and safety outcomes were recurrent VTE and major bleeding, respectively. Other outcomes included the composite of recurrent VTE and major bleeding, clinically relevant nonmajor bleeding (CRNMB), and all-cause mortality. Summary relative risks (RRs) were calculated in a random effects meta-analysis. In the primary analysis comprising 2607 patients, the risk of recurrent VTE was nonsignificantly lower with DOACs than with LMWHs (RR, 0.68; 95% CI, 0.39-1.17). Conversely, the risks of major bleeding (RR, 1.36; 95% CI, 0.55-3.35) and CRNMB (RR, 1.63; 95% CI, 0.73-3.64) were nonsignificantly higher. The risk of the composite of recurrent VTE or major bleeding was nonsignificantly lower with DOACs than with LMWHs (RR, 0.86; 95% CI, 0.60-1.23). Mortality was comparable in both groups (RR, 0.96; 95% CI, 0.68-1.36). Findings were consistent during the on-treatment period and in those with incidental VTE. In conclusion, DOACs are an effective treatment option for patients with cancer and acute VTE, although caution is needed in patients at high risk of bleeding.
AB - Direct oral anticoagulants (DOACs) are an emerging treatment option for patients with cancer and acute venous thromboembolism (VTE), but studies have reported inconsistent results. This systematic review and meta-analysis compared the efficacy and safety of DOACs and low-molecular-weight heparins (LMWHs) in these patients. MEDLINE, Embase, the Cochrane Central Register of Controlled Trials, and conference proceedings were searched to identify relevant randomized controlled trials. Additional data were obtained from the original authors to homogenize definitions for all study outcomes. The primary efficacy and safety outcomes were recurrent VTE and major bleeding, respectively. Other outcomes included the composite of recurrent VTE and major bleeding, clinically relevant nonmajor bleeding (CRNMB), and all-cause mortality. Summary relative risks (RRs) were calculated in a random effects meta-analysis. In the primary analysis comprising 2607 patients, the risk of recurrent VTE was nonsignificantly lower with DOACs than with LMWHs (RR, 0.68; 95% CI, 0.39-1.17). Conversely, the risks of major bleeding (RR, 1.36; 95% CI, 0.55-3.35) and CRNMB (RR, 1.63; 95% CI, 0.73-3.64) were nonsignificantly higher. The risk of the composite of recurrent VTE or major bleeding was nonsignificantly lower with DOACs than with LMWHs (RR, 0.86; 95% CI, 0.60-1.23). Mortality was comparable in both groups (RR, 0.96; 95% CI, 0.68-1.36). Findings were consistent during the on-treatment period and in those with incidental VTE. In conclusion, DOACs are an effective treatment option for patients with cancer and acute VTE, although caution is needed in patients at high risk of bleeding.
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U2 - 10.1182/blood.2020005819
DO - 10.1182/blood.2020005819
M3 - Review article
C2 - 32396939
AN - SCOPUS:85086670116
SN - 0006-4971
VL - 136
SP - 1433
EP - 1441
JO - Blood
JF - Blood
IS - 12
ER -