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. 2023 Aug 8;7(15):4072-4079.
doi: 10.1182/bloodadvances.2022009577.

Survival after cancer-related venous thrombosis: the Scandinavian Thrombosis and Cancer Study

Affiliations

Survival after cancer-related venous thrombosis: the Scandinavian Thrombosis and Cancer Study

Monique J T Crobach et al. Blood Adv. .

Abstract

Patients with cancer have an increased risk of developing venous thromboembolism (VTE), and this combination is reported to result in poorer survival compared with cancer alone. This study aimed to investigate the impact of VTE on the survival of patients with cancer in a general population. The Scandinavian Thrombosis and Cancer (STAC) cohort, a population-based cohort including 144 952 participants without previous VTE or cancer, was used. During follow-up, cancer and VTE incidences were registered. "Cancer-related VTE" was defined as VTE diagnosed in patients with overt or occult cancer. The survival of participants without cancer and/or VTE ("disease-free") was compared with the survival of participants with cancer and cancer-related VTE. Cox regression models with cancer and VTE as time-varying exposures were performed to calculate hazard ratios for death. Subanalyses were performed across cancer types and stages and VTE type (deep vein thrombosis or pulmonary embolism). During follow-up (mean, 11.7 years), 14 621 participants developed cancer, and 2444 developed VTE, of which 1241 were cancer-related. The mortality rates (per 100 person years) for disease-free participants, VTE only, cancer only, and cancer-related VTE were 0.63, 5.0, 9.2, and 45.3, respectively. Compared with patients with cancer only, the risk of death for patients with cancer-related VTE was increased 3.4-fold. Within all cancer types, the occurrence of VTE increased the mortality risk 2.8- to 14.7-fold. In a general population, patients with cancer with VTE had a 3.4-fold higher mortality risk than patients with cancer without VTE, independent of cancer type.

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Conflict of interest statement

Conflict-of-interest disclosure: The authors declare no competing financial interests.

Figures

None
Graphical abstract
Figure 1.
Figure 1.
Classification of exposure categories. Participants were divided into 3 different exposure categories: VTE-exposed, cancer-exposed, and cancer-related VTE–exposed. The date of cancer diagnosis was brought forward by 1 year, assuming that the cancer is already present 1 year before diagnosis. 1, +++ VTE-exposed; 2, ∗∗∗ cancer-exposed; 3a+b, ∞∞∞ cancer-related VTE–exposed.
Figure 2.
Figure 2.
Subanalysis 2: age- and sex-adjusted HRs (95% CI) for mortality for different types of cancer with VTE, compared with the same cancer type without VTE. Date of cancer corrected by 1 year.

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