Predicting Disease Recurrence in Patients with Previous Unprovoked Venous Thromboembolism: The DASH Prediction Score

Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 544-544 ◽  
Author(s):  
Alberto Tosetto ◽  
Alfonso Iorio ◽  
Maura Marcucci ◽  
Trevor Baglin ◽  
Mary Cushman ◽  
...  

Abstract Abstract 544 Background. In patients with unprovoked venous thromboembolism (VTE) occurring in the absence of major provoking factors, the optimal duration of anticoagulation is anchored on estimating the risk for disease recurrence in the individual patient. Evidence from several studies suggests that, at least in selected patient subgroups, the risk for recurrence may approximates the annual risk for anticoagulant-related major hemorrhage, which is estimated at 1–3%, and a recent ISTH consensus considers an annual risk of recurrence below 5% as acceptable to justify stopping anticoagulant therapy. Aim. To develop a clinical prediction guide that stratifies patients according to recurrence risk and, thereby, facilitate decisions about whether to continue or stop anticoagulation. Methods. Individual patient data meta-analysis of 7 prospective studies enrolling patients with a first episode of objectively diagnosed VTE. Eligible VTE cases were those which occurred in the absence of surgery, trauma, active cancer, immobility, or pregnancy and the puerperium. Follow-up started when anticoagulant therapy was stopped and ended when one of the following occurred: symptomatic, objectively documented, recurrent VTE; death from another cause; resumption of anticoagulant therapy for another reason; or the study ended. Predictors were identified using stratified Cox regression, and the weight of predictors was obtained after model shrinkage to correct for over-optimism. The discriminative ability of the prediction rule was estimated using time-dependent c-statistics, and was internally validated by bootstrap analysis. Results. 1818 consecutively referred cases with unprovoked VTE treated for at least three months with a vitamin K antagonist were eligible for analysis. Abnormal D-dimer after stopping anticoagulation, age < 50 years, male sex and VTE not associated with hormonal therapy (in women) were the main predictors of recurrence. Optimism-corrected regression coefficients were used to derive a prognostic recurrence score (DASH, D-dimer, Age, Sex, Hormonal therapy), that showed a good predicting capability (ROC area=0.71). The DASH score attributes the following points: +2 for positive (abnormal) post-anticoagulation D-dimer, +1 for age ≤ 50 years, +1 for male sex, −2 for hormone use at time of initial VTE (in women only). The annualized recurrence risk was 3.1% (95% confidence interval [CI] 2.3 – 3.9) in patients with a DASH score ≤ 1, 6.4% (95% CI 4.8–7.9) in patients with a DASH score 2, and 12.3% (95% CI, 9.9–14.7) in patients with a DASH score ≥ 3, as reported by the Kaplan-Meier recurrence-free survival plot. By considering at low recurrence risk those patients with a DASH score ≤ 1, life-long anticoagulation might be avoided in 51.6% of patients with unprovoked VTE. Conclusions. The DASH score appears to reliably predict recurrence risk in patients with a first unprovoked VTE and may be used to decide whether anticoagulant therapy should be continued indefinitely or stopped after an initial treatment period of at last three months. Patients with a DASH score ≤ 1 appear to have an annual risk for recurrence (3.1%) that may be sufficiently low to justify stopping anticoagulation in an average patient after 3–6 months of anticoagulation, whereas a DASH score ≥ 2 appears to confer a risk of recurrent VTE that may warrant indefinite anticoagulation. Disclosures: No relevant conflicts of interest to declare.

Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 3810-3810
Author(s):  
Martin Ellis ◽  
Martin Mar ◽  
Monreal Manuel ◽  
Orly Hamburger-Avnery ◽  
Alessandra Bura-Riviere ◽  
...  

Abstract Background. Patients with venous thromboembolism (VTE) secondary to transient risk factors or cancer may develop VTE recurrences after discontinuing anticoagulant therapy. Identifying at-risk patients could help to guide the ideal duration of anticoagulant therapy in these patients. Methods. We used the RIETE database to assess the prognostic value of d-dimer testing after discontinuing anticoagulation to identify patients at increased risk for recurrences. The proportion of patients with raised d-dimer levels was determined and the hazard ratio (HR) for VTE recurrences compared to those with normal levels was calculated. Univariate and multivariate analyses of factors associated with VTE recurrence were performed. Results. 3 606 patients were identified in the database in April 2018: 2 590 had VTE after a transient risk factor and 1016 had a cancer. D-dimer levels were measured after discontinuing anticoagulation in 1 732 (67%) patients with transient risk factors and 732 (72%) patients with cancer-associated VTE and these patients formed the cohort in which recurrent VTE rate was calculated. D-dimers and were elevated in 551 (31.8%) of patients with a transient risk factor and were normal in 1181 (68.2%). In the cancer-associated group, d-dimers were elevated in 398 (54.3%) and normal in 334 (45.7%) patients. The adjusted hazard ratio for recurrent VTE was: 2.32 (95%CI: 1.55-3.49) in patients with transient risk factors and 2.23 (95%CI: 1.50-3.39) in those with cancer. Conclusions. Patients with raised d-dimer levels after discontinuing anticoagulant therapy for provoked or cancer-associated VTE are at increased risk for recurrent VTE and death. Future studies could target these patients for extended anticoagulation. Disclosures No relevant conflicts of interest to declare.


Proceedings ◽  
2018 ◽  
Vol 2 (9) ◽  
pp. 528
Author(s):  
A. I. Franco Moreno ◽  
M. J. García Navarro ◽  
C. L. De Ancos Aracil ◽  
A. Gimeno García ◽  
C. Montero Hernández ◽  
...  

Unprovoked venous thromboembolism is associated with a 5 to 27% annual risk of recurrence after discontinuation of anticoagulation, and indefinite anticoagulation is recommended if the bleeding risk is low to moderate. However, in one-third of patients with unprovoked venous thromboembolism, the risk of recurrence is so low (<5% per year) that anticoagulant therapy >3–6 months may not be necessary. Several prediction rules were derived to identify patients with unprovoked venous thromboembolism who have a low recurrence risk. In 2016, we presented our results of the original DAMOVES, a nomogram for prediction of recurrence in an individual patient with unprovoked venous thromboembolism. The aim of this study was to externally validate this nomogram in patients with unprovoked venous thromboembolism.


Blood ◽  
2016 ◽  
Vol 127 (11) ◽  
pp. 1417-1425 ◽  
Author(s):  
Ida Martinelli ◽  
Anthonie W. A. Lensing ◽  
Saskia Middeldorp ◽  
Marcel Levi ◽  
Jan Beyer-Westendorf ◽  
...  

Key Points Estrogen-containing or progestin-only hormonal therapy is not associated with increased recurrent VTE risk in women on anticoagulant therapy. Abnormal uterine bleeding occurred more frequently with rivaroxaban than with enoxaparin/VKAs.


Author(s):  
А.В. Чечулова ◽  
С.И. Капустин ◽  
В.Е. Солдатенков ◽  
В.Д. Каргин ◽  
Л.П. Папаян ◽  
...  

Введение. Наиболее частые клинические проявления венозного тромбоэмболизма (ВТЭ) — тромбоз глубоких вен (ТГВ) и тромбоэмболия легочной артерии (ТЭЛА) — нередко осложняются рецидивом заболевания, который приводит к увеличению риска тяжелого посттромбофлебитического синдрома и/или жизнеугрожающей ТЭЛА. Роль наследственных факторов в развитии рецидива ВТЭ у лиц молодого возраста изучена недостаточно. Цель исследования: поиск генетических факторов риска рецидивирующего течения ВТЭ у пациентов молодого возраста. Материалы и методы. Обследовано 250 пациентов (117 мужчин и 133 женщины, средний возраст — 37,4 года) с ранним дебютом ВТЭ (в возрасте до 45 лет включительно). У 105 (42%) из них наблюдали рецидивирующее течение тромбоза. Всем пациентам было проведено молекулярно-генетическое исследование ДНК-полиморфизма 9 генов, вовлеченных в регуляцию активности плазменного звена гемостаза: α- и β-субъединицы фактора (F) I (Thr312Ala и –455G/A, соответственно), FII (20210 G/A), FV (1691 G/A), FXII (46 C/T), А-субъединицы FXIII (Val34Leu), ингибитора активатора плазминогена 1 типа (PAI-1, —675 4G/5G), тканевого активатора плазминогена (tPA, 311 п. н. Ins/Del) и эндотелиального рецептора протеина С (EPCR, Ser219Gly). Оценку статистической значимости различий в распределении генотипов между группами пациентов с рецидивирующим течением ВТЭ и с единственным эпизодом тромбоза в анамнезе проводили с помощью точного метода Фишера. Результаты. Рецидив ВТЭ в отдаленном периоде был выявлен у 105 (42%) пациентов. Группу сравнения составили 103 (41,2%) пациента с единственным эпизодом ВТЭ в анамнезе. У 42 (16,8%) человек наличие либо отсутствие рецидива установить не удалось. Генотип «tPA Del/Del» встречался в 2 раза реже в группе пациентов с рецидивирующим течением ВТЭ (14,3% против 28,2% у лиц с единственным эпизодом ВТЭ; ОR = 0,4; 95% CI: 0,2–0,9; p = 0,017), что указывает на его возможный протективный эффект от риска рецидива заболевания. Для остальных генов значимых различий в распределении генотипов между сравниваемыми группами не было обнаружено. Изучение «ген-генных взаимодействий» вариантов tPA и PAI-1 выявило существенные различия между группами пациентов: сочетание «tPA Del/Del + + PAI-1 4G5G» в 3,5 раза реже встречалось в группе с рецидивом венозного тромбоза (3,8% против 13,6%; OR = 0,3; 95% CI: 0,08–0,8; p = 0,011), тогда как сочетание генотипов «PAI-1 5G5G + tPA Ins/Del», напротив, было характерно, для этой группы (13,3% против 5,8% у лиц с единственным эпизодом ВТЭ; OR = 2,5; 95% CI: 0,9–6,7; p = 0,054). Заключение. Группа пациентов молодого возраста с рецидивирующим течением ВТЭ характеризуется значительным снижением частоты встречаемости генотипа tPA Del/Del, а также сочетания «tPA Del/Del + PAI-1 4G5G». Для уточнения характера влияния полиморфизма данных генов на риск развития повторных эпизодов ВТЭ необходимы дополнительные исследования. Introduction. The most frequent clinical manifestations of venous thromboembolism (VTE) — deep vein thrombosis (DVT) and pulmonary embolism (PE) are often complicated by recurrent episodes that lead to an increased risk of severe post-thrombophlebitic syndrome and/or life-threatening PE. The role of hereditary factors in the development of recurrent VTE in young people is still unclear. Aim: identifi cation of genetic risk factors for recurrent VTE in young patients. Materials and methods. We examined 250 patients (117 men and 133 women, mean age — 37.4 years) with early VTE debut (aged up to 45 years inclusive). In 105 (42%) of them, a recurring course of thrombosis was observed. In all patients a molecular genetic study of DNA polymorphism of 9 genes involved in the regulation of hemostasis plasma activity was carried out: α-and β-subunits of factor (F) I (Thr312Ala and –455 G/A, respectively), FII (20210 G/A), FV (1691 G/A), FXII (46 C/T), FXIII A subunit (Val34Leu), plasminogen activator inhibitor type I (PAI-1, —675 4G/5G), tissue plasminogen activator (tPA, 311 bp Ins/Del), and the endothelial protein C receptor (EPCR, Ser219Gly). Assessment of statistical signifi cance of diff erences in genotype distribution between the groups of patients with recurrent VTE and a single episode of thrombosis history was performed using Fisher’s exact method. Results. In the long-term period VTE recurrence was revealed in 105 (42%) patients. The comparison group consisted of 103 (41.2%) patients with a single VTE episode in the anamnesis. In 42 (16.8%) patients the presence or absence of disease recurrence was not revealed. Genotype «tPA Del Del» met 2 times less frequently in patients with recurrent VTE (14.3% vs 28.2% in individuals with a single episode of VTE; OR = 0.4; 95% CI: 0,2–0,9; p = 0.017) that indicates its possible protective effect on the risk of disease recurrence. For the remaining genes no signifi cant diff erences in genotypes distribution between the compared groups were found. Study of «gene-gene interactions» of tPA and PAI-1 variants revealed signifi cant differences between groups of patients: the combination «tPA Del/Del + PAI-1 4G5G» was 3.5 times less frequent in the group with recurrent venous thrombosis (3.8% against 13.6%; OR = 0.3; 95% CI: 0.08–0.8; p = 0.011) while the combination of the genotypes «PAI-1 5G5G + tPA Ins/Del», in contrast, was typical for this group (13.3% vs. 5.8% in individuals with a single episode of VTE; OR = 2.5; 95% CI: 0.9–6.7; p = 0.054). Conclusion. Group of young patients with recurrent VTE is characterized by a signifi cant reduction in the incidence of genotype tPA Del/Del as well as the combination of «tPA Del / Del + PAI-1 4G5G». To clarify the eff ect of polymorphism of these genes on the risk of developing of VTE recurrent episodes additional studies are needed.


2015 ◽  
Vol 114 (09) ◽  
pp. 645-650 ◽  
Author(s):  
Rupert Bauersachs ◽  
Jan Beyer-Westendorf ◽  
Henri Bounameaux ◽  
Timothy Brighton ◽  
Alexander Cohen ◽  
...  

SummaryPatients with unprovoked venous thromboembolism (VTE) are at high risk for recurrence. Although rivaroxaban is effective for extended VTE treatment at a dose of 20 mg once daily, use of the 10 mg dose may further improve its benefit-to-risk ratio. Low-dose aspirin also reduces rates of recurrent VTE, but has not been compared with anticoagulant therapy. The EINSTEIN CHOICE study is a multicentre, randomised, double-blind, active-controlled, event-driven study comparing the efficacy and safety of two once daily doses of rivaroxaban (20 and 10 mg) with aspirin (100 mg daily) for the prevention of recurrent VTE in patients who completed 6–12 months of anticoagulant therapy for their index acute VTE event. All treatments will be given for 12 months. The primary efficacy objective is to determine whether both doses of rivaroxaban are superior to aspirin for the prevention of symptomatic recurrent VTE, while the principal safety outcome is the incidence of major bleeding. The trial is anticipated to enrol 2,850 patients from 230 sites in 31 countries over a period of 27 months. In conclusion, the EINSTEIN CHOICE study will provide new insights into the optimal antithrombotic strategy for extended VTE treatment by comparing two doses of rivaroxaban with aspirin (clinicaltrials.gov NCT02064439).


Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 4169-4169
Author(s):  
Neil A. Goldenberg ◽  
Mark Tripputi ◽  
Mark A. Crowther ◽  
Thomas C. Abshire ◽  
Donna M. DiMichele ◽  
...  

Abstract Abstract 4169 The randomized controlled trial (RCT) is the gold-standard clinical trial design by which safety and efficacy of new medical therapies are evaluated in comparison to placebo or established treatments. Randomization serves as a primary means of ensuring equal distribution of confounding factors, minimizing selection bias, and upholding key assumptions of the statistical analysis. In some circumstances, when prognostic heterogeneity is hypothesized but evidence is not definitive, lack of equipoise among experts in the field may preclude randomization in a particular subgroup. In traditional RCT designs, patients in this subpopulation are then excluded from trial participation. However, these patients often constitute an important subgroup of the disease population. By taking advantage of existing RCT infrastructure, efforts to evaluate such patients in a parallel cohort arm – using a “parallel-cohort RCT” design – would provide an efficient means of generating multi-center prospective data on natural history, toward the development of future RCTs involving these subgroups. A current example of the parallel-cohort RCT design is the Kids-DOTT trial, an ongoing investigator-initiated multi-center randomized trial of the duration of anti-thrombotic therapy for venous thrombosis in children. The target population is children with first-episode acute VTE (excluding pulmonary embolism) in whom a reversible prothrombotic clinical risk factor has been identified and comprehensive laboratory assessment reveals no severe or multi-trait thrombophilia. Children meeting eligibility criteria and in whom no persistent occlusive thrombosis at the six-week follow-up time point are randomized to shortened-duration (six weeks) versus conventional-duration (three months) anticoagulant therapy (Figure 1). The primary endpoint is the cumulative incidence (i.e., risk) of recurrent VTE at two years, and will be compared between the two arms. Secondary outcomes include cumulative incidence of post-thrombotic syndrome (PTS) at two years and of major hemorrhage during anticoagulant therapy. The primary hypothesis of the study is that shortened-duration anticoagulation is non-inferior to conventional-duration therapy. The study also evaluates two groups of patients in parallel cohorts (Figure 1). The first group is comprised of patients with a persistent occlusive thrombosis following the first six weeks of anticoagulation; this cohort is allocated to a conventional course of anticoagulation. The second parallel cohort in the Kids-DOTT trial consists of patients with persistent antiphospholipid antibodies, who are allocated to a course of anticoagulation ranging from 3 months to lifelong. For each of these subpopulations, there was lack of equipoise toward inclusion in the randomization to shortened- versus conventional-duration therapy, due to perception of possible increased recurrence risk. The specific aims involving the parallel cohorts are to determine whether: (1) persistent thrombotic veno-occlusion is a prognostic indicator of recurrent VTE and/or PTS, among children treated with a three month conventional course of anticoagulation (comparison of randomization arm B vs. parallel cohort arm C in Figure 1); and (2) duration of therapy influences risk of recurrent VTE and/or PTS among children with persistent APA, when anticoagulated for a minimum duration of three months (within parallel cohort arm D in Figure 1). In this way, the parallel-cohort RCT model of the Kids-DOTT trial provides additional efficiency in trial design, maximizing the information gained from subpopulations of interest that are excluded from randomization. Broader application of the parallel-cohort RCT design should be considered, particularly in rare disease areas, where efforts to maximize inclusion of the diseased population are critical to trial feasibility and applicability. Disclosures: Off Label Use: The presentation refers to the use of anticoagulants as a drug class in general in the treatment of venous thromboembolism (VTE) in children. Despite their use in the standard care for pediatric VTE, all anticoagulants remain off-label for this indication in children.


Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 2301-2301
Author(s):  
kiara Cristina Senger Zapponi ◽  
Luis Fernando Bittar ◽  
Bruna m Mazetto ◽  
Fernanda Dutra Santiago-Bassora ◽  
Fernanda A. Orsi ◽  
...  

Abstract Abstract 2301 Introduction: Venous Thromboembolism (VTE) is a multifactorial disease that affects 1:1000 individuals worldwide, with a recurrence rate of about 25% in 10 years. Although many risk factors for VTE are well defined, first presentation and recurrence depend, at least in part, on as yet unknown etiologic factors. Studies in animal models show a tight relation between inflammation and hemostasis, as well as the infiltration of neutrophils in the venous wall after the induction of venous thrombosis. Neutrophils also participate in different stages in the formation and resolution of venous thrombosis. Methods: In this study, we investigated the adhesive properties of neutrophils in VTE patients. We hypothesized that increased adhesive properties of these cells, either as an individual baseline characteristic or as an acquired alteration after a previous VTE episode, could be associated with the thrombotic process. The patient population consisted of 22 VTE patients (14F:8M; median age: 46.1 years) that had completed at least 6 months of oral anticoagulation. Twenty-two healthy volunteers matched to VTE patients by age, gender and ethnic background were used as controls. Neutrophil adhesion was measured by a static adhesion assay in triplicate. Peripheral blood was collected with heparin and neutrophils were separated on Histopaque® (Sigma-Aldrich, St. Louis, MO, USA). Isolated neutrophils (2.2×106 cells/ml) were allowed to adhere to fibronectin (FN)-coated 96-well plates (30 min, 37°C, 5%CO2). Non-adherent cells were then removed by washing and adherent cells calculated as the percentage of cells adhered, compared to a standard curve of known cell concentrations and using a colorimetric enzyme assay. Results are expressed as means ± standard error of mean (SEM) and were compared using the Mann-Whitney test. Results: Overall, adhesion of neutrophils from VTE patients (25.40% ±2.35) was not increased when compared to the control group (21.25%±1.20 p=0.2). However when only patients at a higher risk of recurrence (n=13) - here defined as the presence of elevated D-dimer (higher than 0.5mg/L) and residual vein thrombosis - were analyzed, a statistically significant increase in cell adhesion compared to matched controls was observed (26.70%±2.08 and 21.36%±1.26, respectively, p = 0.04). When these patients (higher recurrence risk; n=13) were compared to the remaining VTE patients (standard recurrence risk, n=9), a non significant increase in neutrophil adhesion was observed (26.70%±2.08 vs 23.51%±5.03 respectively, p=0.1). Conclusions: We demonstrate that neutrophil adhesion is increased in patients with VTE with characteristics associated with increased recurrence risk. In addition, we also observed a non-significant difference in neutrophil adhesion in these patients compared to other VTE patients. Our results suggest that the increased adhesive properties of neutrophils in VTE patients could play a role in the exacerbation of inflammation, and in the pathophysiology of VTE. Further studies are warranted to study whether neutrophil adhesiveness could be used as a biomarker of VTE recurrence. Disclosures: No relevant conflicts of interest to declare.


Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 3399-3399 ◽  
Author(s):  
Anne Le-Ngoc ◽  
Yunqi Ji ◽  
Vicky Tagalakis

Abstract Abstract 3399 Introduction: Current estimates of cancer risk following acute venous thromboembolism (VTE) vary widely, are based largely on studies with select populations and often include prevalent cancer cases. Objectives: We aimed to determine the incidence and standardized incidence ratio (SIR) of cancer following VTE in a large non-select population. Secondary objectives were to determine time to incident cancer, type of cancer and predictors of cancer. Methods: This retrospective, observational study used the linked administrative healthcare databases of the province of Quebec, Canada, including the province-wide hospitalization database Maintenance et exploitation des données pour l'étude de la clientèle hospitalière (MED-ÉCHO), the vital statistics database of the Institut de la statistique du Québec, and the healthcare services database of the Régie de l'assurance maladie (RAMQ) which is a governmental agency that administers the Quebec universal healthcare program and oversees all physician reimbursement claims. We identified a cohort of patients with a first hospital diagnosis of acute VTE between January 1st, 1994 and December 31, 2004, without a cancer diagnosis in the 24 months prior to the VTE, and who were followed for a minimum of one year until the earliest of either a diagnosis of cancer, occurrence of death, or end of study (December 31st, 2005). Subjects with prevalent cancer (diagnosed within 3 months after VTE) were excluded. VTE cases were classified as unprovoked vs. provoked based on the presence of VTE risk factors in the three months preceding the VTE diagnosis. We determined annual incidence rates of cancer and associated 95% confidence intervals (CI) by dividing the number of cancer cases by the total person-years at risk. Canadian Cancer statistics for the years 1994–2005 were used to calculate the SIRs. Results: Among 39 222 patients with first-time VTE and without a diagnosis of cancer in the previous 24 months, 3 062 (7.8%) were diagnosed with cancer during a mean follow-up of 65.2 months [standard deviation (SD) =39.1], for an annual incidence rate of 1.55 (95% CI 1.49–1.60) per 100 person-years. Mean time to cancer diagnosis following VTE was 40.5 months (SD=32.3). Gastrointestinal (25.7%), genitourinary (25.7%) and pulmonary (19.6%) malignancies were most frequent. The SIR for any cancer was 3.55 (95% CI 3.43–3.68). Table 1 shows the SIRs by cancer type. Clinical predictors for cancer were male sex [hazard ratio (HR) 1.59 (95% CI 1.49–1.72)], increasing age [HR 1.53 (95% CI 1.49–1.57)] and increasing comorbidity [HR 1.04 (95% CI 1.01–1.06)]. The annual risk for cancer was 1.7 times higher in patients with provoked compared to patients with unprovoked VTE [1.94 (95% CI 1.86–2.03) vs. 1.15 (95% CI 1.09–1.22) per 100 person-years, respectively]. Compared to patients with unprovoked VTE, patients with provoked VTE were older [61.9 mean years (SD=18.3) vs. 56.6 mean years (SD=18.4); p<0.001] and had a higher Charlson comorbidity index weighted score [1.19 (SD=1.57) vs. 0.62 (SD=1.12); p<0.001]. Conclusion: In patients with acute VTE and without previous or prevalent cancer, the annual risk of cancer is 1.55%, which is higher than the risk in the general population. The mean time to cancer diagnosis is about 3.4 years. Male sex, advanced age, and increasing comorbid conditions are associated with a diagnosis of cancer. Advanced age and a higher burden of comorbid conditions may explain the higher incidence of cancer observed in patients with provoked VTE compared to patients with unprovoked VTE. Clinicians should be aware of the associated long-term risk of cancer in patients presenting with acute VTE. Disclosures: No relevant conflicts of interest to declare.


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