Long-term bleeding events post-percutaneous coronary intervention in patients with malignancy with and without anticoagulant therapy

The prevalence of malignancies in patients undergoing percutaneous coronary intervention (PCI) is increasing with aging. Active malignancy is a significant contributor to high bleeding risk. For cancer patients requiring oral anticoagulant (OAC) therapy, the choice between direct oral anticoagulants (DOAC) and warfarin is critical. The aim of this study was to investigate long-term bleeding events in patients with malignancy undergoing PCI. The CLIDAS (Clinical Deep Data Accumulation System) multicenter database includes data from seven tertiary medical hospitals in Japan. This retrospective analysis included 6451 patients who underwent PCI between April 2013 and March 2019 and completed 3-year follow-up. The patients were divided into two groups; No malignancy (n = 5787) and Malignancy group (n = 664). Malignancy was defined by a history of cancer treatment. These groups were further subcategorized based on OAC therapy; (1) No malignancy without OAC (n = 5134), (2) No malignancy with DOAC (n = 261), (3) No malignancy with warfarin (n = 392), (4) Malignancy without OAC (n = 589), (5) Malignancy with DOAC (n = 38), and (6) Malignancy with warfarin (n = 37). The primary outcome was the incidence of bleeding events, defined according to the Global Use of Streptokinase and t-PA for Occluded Coronary Arteries classification of moderate and severe bleeding. The secondary outcomes were major adverse cardiac events (MACE) and net adverse clinical events (NACE). Multivariable Cox regression analysis showed that the malignancy with warfarin group had a significantly higher risk of bleeding events compared to the malignancy without OAC group (hazard ratio [HR], 3.64; 95% confidence interval [CI], 1.38-9.61, p value = 0.009). No significant differences were observed for MACE (HR, 1.39; 95% CI 0.59-3.25, p value = 0.454) or NACE (HR, 1.62; 95% CI, 0.80-3.29; p value = 0.184). Malignancy patients receiving warfarin were associated with a higher risk of bleeding events. DOACs may represent a preferable alternative to warfarin with regard to bleeding risk in patients with malignancy undergoing PCI.

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Publication Details

Journal
Cardiovascular Intervention and Therapeutics
Published
2025-06-09
DOI
https://doi.org/10.1007/s12928-025-01151-4
Citations
2
Primary Topic
Venous Thromboembolism Diagnosis and Management
Type
article
Field-Weighted Citation Impact
3.74

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article

Long-term bleeding events post-percutaneous coronary intervention in patients with malignancy with and without anticoagulant therapy

Masanobu Ishii, Yasuhiro Otsuka, Takahide Kohro, Hideo Fujita et al.
2 citations
Cardiovascular Intervention and Therapeutics
Venous Thromboembolism Diagnosis and Management
3.74
article

Long-term bleeding events post-percutaneous coronary intervention in patients with malignancy with and without anticoagulant therapy

Masanobu Ishii, Yasuhiro Otsuka, Takahide Kohro, Hideo Fujita, Kazuomi Kario, Hisahiko Sato, Tomoyuki Kabutoya, Kenichi Tsujita, Tatsuya Tokai, Takamasa Iwai, Kotaro Nochioka, Taishi Nakamura, Masaaki Nakayama, Yusuke Oba, Yoshihiro Miyamoto, Naoyuki Akashi, Tetsuya Matoba, So Ikebe, Yoshiko Mizuno, Yasuhiro Nakano, Yasushi Imai, Arihiro Kiyosue, Ryozo Nagai
article en
2 citations

Abstract

The prevalence of malignancies in patients undergoing percutaneous coronary intervention (PCI) is increasing with aging. Active malignancy is a significant contributor to high bleeding risk. For cancer patients requiring oral anticoagulant (OAC) therapy, the choice between direct oral anticoagulants (DOAC) and warfarin is critical. The aim of this study was to investigate long-term bleeding events in patients with malignancy undergoing PCI. The CLIDAS (Clinical Deep Data Accumulation System) multicenter database includes data from seven tertiary medical hospitals in Japan. This retrospective analysis included 6451 patients who underwent PCI between April 2013 and March 2019 and completed 3-year follow-up. The patients were divided into two groups; No malignancy (n = 5787) and Malignancy group (n = 664). Malignancy was defined by a history of cancer treatment. These groups were further subcategorized based on OAC therapy; (1) No malignancy without OAC (n = 5134), (2) No malignancy with DOAC (n = 261), (3) No malignancy with warfarin (n = 392), (4) Malignancy without OAC (n = 589), (5) Malignancy with DOAC (n = 38), and (6) Malignancy with warfarin (n = 37). The primary outcome was the incidence of bleeding events, defined according to the Global Use of Streptokinase and t-PA for Occluded Coronary Arteries classification of moderate and severe bleeding. The secondary outcomes were major adverse cardiac events (MACE) and net adverse clinical events (NACE). Multivariable Cox regression analysis showed that the malignancy with warfarin group had a significantly higher risk of bleeding events compared to the malignancy without OAC group (hazard ratio [HR], 3.64; 95% confidence interval [CI], 1.38-9.61, p value = 0.009). No significant differences were observed for MACE (HR, 1.39; 95% CI 0.59-3.25, p value = 0.454) or NACE (HR, 1.62; 95% CI, 0.80-3.29; p value = 0.184). Malignancy patients receiving warfarin were associated with a higher risk of bleeding events. DOACs may represent a preferable alternative to warfarin with regard to bleeding risk in patients with malignancy undergoing PCI.

Cardiovascular Intervention and TherapeuticsVol. 40(4)
Kyushu University (JP), Jichi Medical University (JP), Development Bank of Japan (JP), Tohoku University (JP), Tohoku University Hospital (JP), Miyazaki Prefectural Hospital (JP), University of Tokyo Hospital (JP), National Cerebral and Cardiovascular Center (JP), Jichi Medical University Saitama Medical Center (JP), Kumamoto University (JP)
Kowa Company, Kumamoto University
Good health and well-being
Openalex Percentile: Top 7%
Venous Thromboembolism Diagnosis and Management
3.74
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