Perinatal and familial risk factors for soft tissue sarcomas in childhood through young adulthood: A population‐based assessment in 4 million live births.

Autor: Lupo, Philip J., Luna‐Gierke, Ruth E., Chambers, Tiffany M., Tavelin, Björn, Scheurer, Michael E., Melin, Beatrice, Papworth, Karin
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Zdroj: International Journal of Cancer; Feb2020, Vol. 146 Issue 3, p791-802, 12p
Abstrakt: Perinatal factors have been associated with soft tissue sarcomas (STS) in case‐control studies. However, (i) the contributions of factors including fetal growth remain unknown, (ii) these factors have not been examined in cohort studies and (iii) few assessments have evaluated risk in specific STS subtypes. We sought to identify the role of perinatal and familial factors on the risk of STS in a large population‐based birth cohort. We identified 4,023,436 individuals in the Swedish Birth Registry born during 1973–2012. Subjects were linked to the Swedish Cancer Registry, where incident STS cases were identified. We evaluated perinatal and familial factors obtained from Statistics Sweden, including fetal growth, gestational age, and presence of a congenital malformation. Poisson regression was used to estimate incidence rate ratios (IRRs) and 95% confidence intervals (CIs) for associations between perinatal factors and STS overall, as well as by common subtypes. There were 673 individuals diagnosed with STS in 77.5 million person‐years of follow‐up. Having a congenital malformation was associated with STS (IRR = 1.70, 95% CI: 1.23–2.35). This association was stronger (IRR = 2.90, 95% CI: 1.25–6.71) in recent years (2000–2012). Low fetal growth was also associated with STS during the same time period (IRR = 1.86, 95% CI: 1.05–3.29). Being born preterm was associated with rhabdomyosarcoma (IRR = 1.74, 95% CI: 1.08–2.79). In our cohort study, those with congenital malformations and other adverse birth outcomes were more likely to develop a STS compared to their unaffected contemporaries. These associations may point to disrupted developmental pathways and genetic factors influencing the risk of STS. What's new? Pediatric soft tissue sarcomas (STS) are difficult to study because they are very rare as well as heterogeneous. Now, large cancer registries open the door to studying ever rarer conditions. Here, the authors evaluated the impact of perinatal factors on STS in children and young adults. Using data from Statistics Sweden, they collected perinatal information for 673 individuals diagnosed with STS. Having a congenital malformation, they found, was strongly associated with STS. They also found associations with low fetal weight and younger maternal age. Based on these associations, they suggest that developmental disruptions may boost the risk of STS. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index