Semin Thromb Hemost 2018; 44(04): 370-376
DOI: 10.1055/s-0037-1607436
Review Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Use of Non–Vitamin K Antagonist Oral Anticoagulants in Atrial Fibrillation Patients with Malignancy: Clinical Practice Experience in a Single Institution and Literature Review

Vincenzo Russo
1   Department of Cardiology, University of Campania “Luigi Vanvitelli,” Monaldi Hospital, Naples, Italy
,
Anna Rago
1   Department of Cardiology, University of Campania “Luigi Vanvitelli,” Monaldi Hospital, Naples, Italy
,
Andrea Antonio Papa
1   Department of Cardiology, University of Campania “Luigi Vanvitelli,” Monaldi Hospital, Naples, Italy
,
Federica Di Meo
1   Department of Cardiology, University of Campania “Luigi Vanvitelli,” Monaldi Hospital, Naples, Italy
,
Emilio Attena
2   Department of Cardiology, Fatebenefratelli Hospital, Naples, Italy
,
Paolo Golino
1   Department of Cardiology, University of Campania “Luigi Vanvitelli,” Monaldi Hospital, Naples, Italy
,
Antonio D'Onofrio
3   Departmental Unit of Electrophysiology, Evaluation and Treatment of Arrhythmias, Monaldi Hospital, Naples, Italy
,
Gerardo Nigro
1   Department of Cardiology, University of Campania “Luigi Vanvitelli,” Monaldi Hospital, Naples, Italy
› Author Affiliations
Further Information

Publication History

Publication Date:
08 December 2017 (online)

Abstract

This observational study aimed to investigate the efficacy and safety of non–vitamin K antagonist oral anticoagulants (NOACs) in atrial fibrillation (AF) patients with malignancy. A total of 76 patients (mean age: 73.2 ± 8.9; 28 females) with AF and malignancy treated with NOAC were included in the analysis. The mean CHA2DS2-VASc and HAS-BLED scores were 3.2 ± 1.2 and 2.2 ± 0.9, respectively. The study population was taking dabigatran 150 mg (25%) twice daily (BID), apixaban 5 mg BID (25%), dabigatran 110 mg BID (24%), rivaroxaban 20 mg (18%) once a day (OD), rivaroxaban 15 mg OD (5%), or apixaban 2.5 mg OD (3%). NOAC therapy began, on average, 248 ± 238 days before malignancy diagnosis for an average duration of 1,000 ± 289 days. Stroke, transient ischemic attack, major and minor bleeding events, other adverse effects, and major cardiovascular complications during the follow-up period were collected. In our study population, no patients experienced thromboembolic events during therapy with any NOAC. We recorded a low global incidence of major bleeding (3.9%) with a mean annual incidence of 1.4%. No hemorrhagic stroke or subarachnoid hemorrhage was observed. Only nine patients (11.8%) experienced minor bleeding. According to our data, anticoagulation therapy with NOACs seems to be an effective and safe treatment strategy for nonvalvular AF patients with malignancy.

 
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