7 research outputs found
Early childhood leukemia incidence trends in Brazil
<p>Incidence rates of childhood leukemia vary between different regions of the world. The objective of this study was to test possible trends in incidence rate of early childhood leukemia (children <5 years old at the diagnosis) in Brazil. Data from 18 population-based cancer registries (PBCRs) were analyzed (period 1999–2010). The analysis consisted of frequencies, age-adjusted incidence rates, and joinpoint regression results, including annual average percent change (AAPC) in incidence rates and 95% confidence intervals (CIs). The median age-adjusted incidence rate (AAIR) of overall early childhood leukemia was 61 per million. The AAIR for acute lymphoid leukemia (ALL) was 44 per million and nonlymphoid acute leukemia (NLAL) was 14 per million. The median ALL/NLAL ratio was 3.0, suggesting higher incidence rate of NLAL in these settings. The joinpoint analysis demonstrated increased leukemia incidence rate in João Pessoa (AAPC = 20; 95% CI: 3.5, 39.4) and Salvador (AAPC = 8.68; 95% CI: 1.0, 16.9), respectively, whereas incidence rate in São Paulo PBCR decreased (AAPC = −4.02%; 95% CI: −6.1%, −1.9%). Correlation between ALL AAIR and selected variables of socioeconomic (SES) factors was not observed. Increased AAIR regionally overtime was observed. However, the interpretation for such phenomenon should be cautious because it might reflect the access to health care, diagnosis procedures, and improvement of PBCR´s quality. The observed trend supports the necessity of further ecological studies.</p
Additional file 1: Figure S1. of Association between long interspersed nuclear element-1 methylation levels and relapse in Wilms tumors
LINE-1 methylation pyrograms of representative samples. (A) Normal kidney; (B) Wilms tumor. Five CpG sites were evaluated in the LINE-1 promoter sequence. Arrows indicate internal controls for bisulfite conversion. (TIFF 416Â kb
Risk estimates for sociodemographic, maternal, pre and perinatal factors and embryonal tumors, Brazil 2000–2010.
<p>Risk estimates for sociodemographic, maternal, pre and perinatal factors and embryonal tumors, Brazil 2000–2010.</p
Additional file 2: Table S1. of Association between long interspersed nuclear element-1 methylation levels and relapse in Wilms tumors
Updated clinical data and methylation mean of the 5 LINE-1 sites of each patient. (DOCX 33Â kb
Sociodemographic, maternal, pre and perinatal characteristics of childhood embryonal tumors and controls, Brazil, 2000–2010.
<p>Sociodemographic, maternal, pre and perinatal characteristics of childhood embryonal tumors and controls, Brazil, 2000–2010.</p
Risk estimates for sociodemographic, maternal, pre and perinatal factors and embryonal tumors according to age strata, Brazil 2000–2010.
<p>Risk estimates for sociodemographic, maternal, pre and perinatal factors and embryonal tumors according to age strata, Brazil 2000–2010.</p
Adjusted Risk Estimates for Maternal and Perinatal Characteristics and Pediatric Tumors According to Subtypes, Brazil 2000–2010.
<p>(A) Adjusted<sup>a</sup> risk estimates for Apgar 5-level ≤8 and pediatric tumors. (B) Adjusted<sup>b</sup> risk estimates for continuous birth order-per order of 1 and pediatric tumors. (C) Adjusted<sup>b</sup> risk estimates for mode of delivery-cesarean and pediatric tumors. (D) Adjusted<sup>b</sup> risk estimates for maternal education level ≥12 years and pediatric tumors. OR—Odds Ratio; CI—Confidence Interval; <sup>a</sup>Adjusted by sex, birth weight and birth anomalies; <sup>b</sup> Adjusted by maternal education, sex, birth weight and birth anomalies; *Include CNS tumors, retinoblastoma, neuroblastoma, renal tumors, germ cell tumors, hepatoblastoma and soft tissue sarcoma.</p