Impact of Anemia on Clinical Outcomes of Patients With Cancer-Associated Isolated Distal Deep Vein Thrombosis Receiving Edoxaban - Insights From the ONCO DVT Study.

Anemia Bleeding Cancer-associated thrombosis Edoxaban Venous thromboembolism

Journal

Circulation journal : official journal of the Japanese Circulation Society
ISSN: 1347-4820
Titre abrégé: Circ J
Pays: Japan
ID NLM: 101137683

Informations de publication

Date de publication:
19 Sep 2024
Historique:
medline: 19 9 2024
pubmed: 19 9 2024
entrez: 18 9 2024
Statut: aheadofprint

Résumé

The ONCO DVT study demonstrated potential benefits of extended edoxaban treatment in patients with isolated distal deep vein thrombosis in terms of thrombotic risk. However, the risk-benefit balance in patients with anemia remains unclear. This prespecified subgroup analysis included 601 patients, divided into anemia (n=402) and no-anemia (n=199) groups. The primary endpoint was symptomatic recurrent venous thromboembolism (VTE) or VTE-related death. Anemia was defined as hemoglobin <12 g/dL for women and <13 g/dL for men. In the anemia subgroup, the primary endpoint occurred in 3 (1.5%) and 17 (8.4%) patients in the 12- and 3-month edoxaban treatment groups, respectively (odds ratio [OR] 0.17; 95% confidence interval [CI] 0.05-0.58), compared with 0 and 5 (4.9%) patients, respectively, in the no-anemia subgroup (P interaction=0.997). Major bleeding occurred in 26 (13.1%) and 17 (8.4%) patients with anemia in the 12- and 3-month edoxaban treatment groups, respectively (OR 1.64; 95% CI 0.86-3.14), compared with 2 (2.1%) and 5 (4.9%) patients without anemia (OR 0.67; 95% CI 0.26-1.73; P interaction=0.13). Regardless of the presence of anemia, edoxaban treatment for 12 months was superior to treatment for 3 months in reducing thrombotic events, whereas the risk of major bleeding did not differ significantly between the 2 treatment groups.

Sections du résumé

BACKGROUND BACKGROUND
The ONCO DVT study demonstrated potential benefits of extended edoxaban treatment in patients with isolated distal deep vein thrombosis in terms of thrombotic risk. However, the risk-benefit balance in patients with anemia remains unclear.
METHODS AND RESULTS RESULTS
This prespecified subgroup analysis included 601 patients, divided into anemia (n=402) and no-anemia (n=199) groups. The primary endpoint was symptomatic recurrent venous thromboembolism (VTE) or VTE-related death. Anemia was defined as hemoglobin <12 g/dL for women and <13 g/dL for men. In the anemia subgroup, the primary endpoint occurred in 3 (1.5%) and 17 (8.4%) patients in the 12- and 3-month edoxaban treatment groups, respectively (odds ratio [OR] 0.17; 95% confidence interval [CI] 0.05-0.58), compared with 0 and 5 (4.9%) patients, respectively, in the no-anemia subgroup (P interaction=0.997). Major bleeding occurred in 26 (13.1%) and 17 (8.4%) patients with anemia in the 12- and 3-month edoxaban treatment groups, respectively (OR 1.64; 95% CI 0.86-3.14), compared with 2 (2.1%) and 5 (4.9%) patients without anemia (OR 0.67; 95% CI 0.26-1.73; P interaction=0.13).
CONCLUSIONS CONCLUSIONS
Regardless of the presence of anemia, edoxaban treatment for 12 months was superior to treatment for 3 months in reducing thrombotic events, whereas the risk of major bleeding did not differ significantly between the 2 treatment groups.

Identifiants

pubmed: 39293971
doi: 10.1253/circj.CJ-24-0571
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Shinya Fujiki (S)

Department of Cardiovascular and Medicine, Niigata University Graduate School of Medical and Dental Sciences.

Yugo Yamashita (Y)

Department of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University.

Takeshi Morimoto (T)

Department of Clinical Epidemiology, Hyogo Medical University.

Nao Muraoka (N)

Division of Cardiology, Shizuoka Cancer Center.

Michihisa Umetsu (M)

Division of Vascular Surgery, Department of Surgery, Tohoku University Hospital.

Yuji Nishimoto (Y)

Division of Cardiology, Osaka General Medical Center.

Takuma Takada (T)

Department of Cardiology, Tokyo Women's Medical University.

Yoshito Ogihara (Y)

Department of Cardiology and Nephrology, Mie University Graduate School of Medicine.

Tatsuya Nishikawa (T)

Department of Onco-Cardiology, Osaka International Cancer Institute.

Nobutaka Ikeda (N)

Division of Cardiovascular Medicine, Toho University Ohashi Medical Center.

Kazunori Otsui (K)

Department of General Internal Medicine, Kobe University Graduate School of Medicine.

Daisuke Sueta (D)

Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University.

Yukari Tsubata (Y)

Department of Internal Medicine, Division of Medical Oncology and Respiratory Medicine, Shimane University Faculty of Medicine.

Masaaki Shoji (M)

Department of Cardiovascular Medicine, National Cancer Center Hospital.

Ayumi Shikama (A)

Department of Obstetrics and Gynecology, Faculty of Medicine, University of Tsukuba.

Yutaka Hosoi (Y)

Department of Cardiovascular Surgery, Kyorin University Faculty of Medicine.

Yasuhiro Tanabe (Y)

Department of Cardiology, St. Marianna University School of Medicine.

Ryuki Chatani (R)

Department of Cardiovascular Medicine, Kurashiki Central Hospital.

Kengo Tsukahara (K)

Division of Cardiology, Fujisawa City Hospital.

Naohiko Nakanishi (N)

Department of Cardiovascular Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine.

Kitae Kim (K)

Department of Cardiovascular Medicine, Kobe City Medical Center General Hospital.

Satoshi Ikeda (S)

Department of Cardiovascular Medicine, Nagasaki University Graduate School of Biomedical Sciences.

Takeshi Kimura (T)

Department of Cardiology, Hirakata Kohsai Hospital.

Takayuki Inomata (T)

Department of Cardiovascular and Medicine, Niigata University Graduate School of Medical and Dental Sciences.

Classifications MeSH