Key result
A high ThroLy score was significantly associated with VTE development (OR 5.13; 95% CI 1.83-14.36; P=0.002), but the score was not suitably accurate as 48% of VTE events occurred in low-risk patients.
Why the study?
Does the ThroLy score accurately predict venous thromboembolism in patients treated for lymphoid malignancies?
Cohort (n=428)
Does the ThroLy score accurately predict venous thromboembolism in patients treated for lymphoid malignancies?
Odds Ratio: 5.13 (95% CI 1.83–14.36)
Absolute Event Rate: 38.9% vs 9.6%
p-value: p=0.002
The ThroLy score demonstrated poor predictive accuracy for VTE in patients with DLBCL or HL undergoing first-line chemotherapy, as nearly half of all VTE events occurred in patients classified as low risk.
ThroLy score may aid VTE risk stratification in ambulatory lymphoma patients; leaves open prospective validation before practice change.
The utility in clinical practice of a recently developed and validated predictive model for venous thromboembolism (VTE) events in lymphoma patients, known as the thrombosis lymphoma (ThroLy) score, is unknown. We evaluated the association of ThroLy with VTE in patients treated for diffuse large B-cell lymphoma (DLBCL) or Hodgkin lymphoma (HL) undergoing ambulatory first-line chemotherapy. Retrospective analyses were performed on 428 patients (median age 50), 241 were newly diagnosed DLBCL, and 187 had HL. During initial chemotherapy, 64 (15%) patients developed VTE. According to the ThroLy, 322 (75.2%) patients were considered low risk, 88 (20.6%) patients had intermediate risk and 18 (4.2%) patients high risk for VTE development. Patients with DLBCL were more often in the high-risk ThroLy group and had more VTE events than HL. VTE occurred in; 38.9% (n = 7) high-risk patients, 29.5% (n = 26) intermediate risk, and 9.6% (n = 31) low risk according to the ThroLy score. However, in multivariate analysis, high ThroLy (OR 5.13; 95% CI: 1.83-14.36, P = .002), intermediate ThroLy (OR 3.96; 95% CI: 2.19-7.17, P < .001), and aggressive lymphoma-DLBCL (OR 1.91; 95% CI: 1.05-3.47, P = .034) were all significantly associated with development of VTE, 48% of the VTE events occurred in the low-risk ThroLy score group (the ROC AUC (95% CI) 0.40-0.70 and C statistic-0.55). In our study, the ThroLy score was not a suitably accurate model for predicting VTE events in patients at higher risk of VTE. Further research should be conducted to identify new biomarkers that will predict these events and to establish a new VTE risk assessment model.
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Rupa‐Matysek et al. (2018) conducted a cohort in Diffuse large B-cell lymphoma (DLBCL) or Hodgkin lymphoma (HL) (n=428). High ThroLy score vs. Low ThroLy score was evaluated on Venous thromboembolism (VTE) (OR 5.13, 95% CI 1.83-14.36, p=0.002). A high ThroLy score was significantly associated with VTE development (OR 5.13; 95% CI 1.83-14.36; P=0.002), but the score was not suitably accurate as 48% of VTE events occurred in low-risk patients.
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