1999
DOI: 10.1007/pl00014341
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Clinical relevance of genetic risk factors for thrombosis in paediatric oncology patients with central venous catheters

Abstract: Genetic mutations appear to be additional risk factors for the development of thrombosis in patients with ALL. In contrast, these mutations do not appear to be relevant risk factors for thrombosis in the small number of children with other malignant diseases reported here. This difference may be due to asparaginase and corticosteroids being used in ALL but not in solid tumour protocols.

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Cited by 95 publications
(94 citation statements)
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“…In agreement with these findings, Riordan and colleagues [19] found a low prevalence of factor V Leiden gene mutation in 28 cancer patients with catheter-related venous thrombosis. In contrast, other groups did find an association between factor V Leiden and prothrombin gene mutations and thrombosis in paediatric [20] and in adult patients with haematological malignancies [21]. One explanation could be that gene mutations only carry a low additional risk that does not have a substantial impact on thrombosis incidence when other factors already result in a high incidence of venous thrombosis.…”
Section: Discussionmentioning
confidence: 87%
“…In agreement with these findings, Riordan and colleagues [19] found a low prevalence of factor V Leiden gene mutation in 28 cancer patients with catheter-related venous thrombosis. In contrast, other groups did find an association between factor V Leiden and prothrombin gene mutations and thrombosis in paediatric [20] and in adult patients with haematological malignancies [21]. One explanation could be that gene mutations only carry a low additional risk that does not have a substantial impact on thrombosis incidence when other factors already result in a high incidence of venous thrombosis.…”
Section: Discussionmentioning
confidence: 87%
“…Prothrombotic genetic defects were investigated in 557 children (5 studies). 42,43,70,71,75 Thirtyone events were observed in 113 patients affected by at least one prothrombotic genetic risk factor (factor V 1691GϾA mutation, prothrombin 20210GϾA variant, TT677 methylenetetrahydrofolate reductase [MTHFR] genotype, deficiency of protein C, protein S, antithrombin, elevated lipoprotein [a]). As only one study measured antiphospholipid antibodies (APLAs), 70 this acquired prothrombotic condition was not included in the analysis.…”
Section: Type Of Steroidsmentioning
confidence: 99%
“…Four of the six patients with leukemia and thrombosis (67%) but only 21% of leukemia patients without thrombosis had a genetic risk factor (P < 0.013, chi2). No genetic defect was found in the four patients with other solid malignancies and thrombosis (25). A prothrombotic risk factor or a direct cause is identified in about 85% of the patients with sinus thrombosis.…”
Section: Discussionmentioning
confidence: 81%