Ethnicity, race, and socioeconomic status influence incidence of langerhans cell histiocytosis. Issue 6 (13th January 2015)
- Record Type:
- Journal Article
- Title:
- Ethnicity, race, and socioeconomic status influence incidence of langerhans cell histiocytosis. Issue 6 (13th January 2015)
- Main Title:
- Ethnicity, race, and socioeconomic status influence incidence of langerhans cell histiocytosis
- Authors:
- Ribeiro, Karina Braga
Degar, Barbara
Antoneli, Célia Beatriz Gianotti
Rollins, Barrett
Rodriguez‐Galindo, Carlos - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25404-sec-0001" sec-type="section"> <title>Background</title> <p>Langerhans cell histiocytosis (LCH) is a rare disease, and its etiology is not well understood. Population‐based studies may contribute to etiologic research by defining incidence patterns. This study was designed to evaluate the descriptive epidemiology of disseminated LCH in the United States, using data from population‐based cancer registries.</p> </sec> <sec id="pbc25404-sec-0002" sec-type="section"> <title>Procedure</title> <p>We analyzed the incidence and survival of disseminated LCH in children and adolescents (0–19 years) from 18 SEER registries during 2000–2009. Age‐standardized incidence rates (ASIR) per million and rate ratios (RR) were calculated by gender, race, ethnicity, age, and socioeconomic variables (crowding, rural/urban, education, and poverty) using the SEER*Stat software 8.0.1. Relative survival (RS) estimates were calculated using Ederer II method.</p> </sec> <sec id="pbc25404-sec-0003" sec-type="section"> <title>Results</title> <p>One hundred forty‐five cases of disseminated LCH were recorded; ASIR was 0.70/million per year. Lower ASIR was observed for blacks (vs. whites) (RR = 0.41, 95% CI 0.18–0.81), while higher ASIR was noted for Hispanics (vs. non‐Hispanics) (RR = 1.63, 95% CI 1.15–2.29). Risk of LCH was higher in crowded counties (RR = 1.84, 95% CI 1.31–2.58) and also in<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25404-sec-0001" sec-type="section"> <title>Background</title> <p>Langerhans cell histiocytosis (LCH) is a rare disease, and its etiology is not well understood. Population‐based studies may contribute to etiologic research by defining incidence patterns. This study was designed to evaluate the descriptive epidemiology of disseminated LCH in the United States, using data from population‐based cancer registries.</p> </sec> <sec id="pbc25404-sec-0002" sec-type="section"> <title>Procedure</title> <p>We analyzed the incidence and survival of disseminated LCH in children and adolescents (0–19 years) from 18 SEER registries during 2000–2009. Age‐standardized incidence rates (ASIR) per million and rate ratios (RR) were calculated by gender, race, ethnicity, age, and socioeconomic variables (crowding, rural/urban, education, and poverty) using the SEER*Stat software 8.0.1. Relative survival (RS) estimates were calculated using Ederer II method.</p> </sec> <sec id="pbc25404-sec-0003" sec-type="section"> <title>Results</title> <p>One hundred forty‐five cases of disseminated LCH were recorded; ASIR was 0.70/million per year. Lower ASIR was observed for blacks (vs. whites) (RR = 0.41, 95% CI 0.18–0.81), while higher ASIR was noted for Hispanics (vs. non‐Hispanics) (RR = 1.63, 95% CI 1.15–2.29). Risk of LCH was higher in crowded counties (RR = 1.84, 95% CI 1.31–2.58) and also in areas with low educational level (RR = 1.49, 95% CI 1.02–2.22). Five‐year relative survival was 90.0% (95% CI 83.0–94.2). Important differences in survival were noted according to gender (male: RS = 96.0 vs. female: RS = 83.4%, <italic>P</italic> = 0.029) and age (&lt;1 year: RS = 78.5, 1–4 years: RS = 95.6%, 5–19 years: RS = 100%, <italic>P</italic> = 0.004).</p> </sec> <sec id="pbc25404-sec-0004" sec-type="section"> <title>Conclusions</title> <p>This population‐based study shows significant variations in the incidence of disseminated LCH by race and ethnic group, as well as the influence of socioeconomic factors. These data may provide clues to causation and point toward the need for analytical epidemiologic studies. Pediatr Blood Cancer 2015;62:982–987. © 2015 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric blood & cancer. Volume 62:Issue 6(2015:Jun.)
- Journal:
- Pediatric blood & cancer
- Issue:
- Volume 62:Issue 6(2015:Jun.)
- Issue Display:
- Volume 62, Issue 6 (2015)
- Year:
- 2015
- Volume:
- 62
- Issue:
- 6
- Issue Sort Value:
- 2015-0062-0006-0000
- Page Start:
- 982
- Page End:
- 987
- Publication Date:
- 2015-01-13
- Subjects:
- Tumors in children -- Periodicals
Blood -- Diseases -- Periodicals
Cancer in children -- Periodicals
618.92 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1545-5017 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pbc.25404 ↗
- Languages:
- English
- ISSNs:
- 1545-5009
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.533500
British Library DSC - BLDSS-3PM
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- 4126.xml