Comparison of survival at adult versus pediatric treatment centers for rare pediatric tumors in an adolescent and young adult (AYA) population in the state of Georgia. Issue 3 (12th November 2014)
- Record Type:
- Journal Article
- Title:
- Comparison of survival at adult versus pediatric treatment centers for rare pediatric tumors in an adolescent and young adult (AYA) population in the state of Georgia. Issue 3 (12th November 2014)
- Main Title:
- Comparison of survival at adult versus pediatric treatment centers for rare pediatric tumors in an adolescent and young adult (AYA) population in the state of Georgia
- Authors:
- Cash, Thomas
Qayed, Muna
Ward, Kevin C.
Mertens, Ann C.
Rapkin, Louis - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25326-sec-0001" sec-type="section"> <title>Background</title> <p>The type of treatment center where 15–21‐year‐old adolescent and young adult (AYA) patients with rare pediatric tumors achieve their best clinical outcome is unknown.</p> </sec> <sec id="pbc25326-sec-0002" sec-type="section"> <title>Procedure</title> <p>We performed a retrospective analysis using the Georgia Cancer Registry (GCR) of 15–21‐year old patients with a malignant, rare pediatric tumor diagnosed during the period from 2000–2009. Patients were identified as being treated at one of five Georgia pediatric cancer centers or at an adult center. Data were analyzed for 10 year overall survival, patient characteristics associated with death, and patient characteristics present at diagnosis associated with choice of treatment center.</p> </sec> <sec id="pbc25326-sec-0003" sec-type="section"> <title>Results</title> <p>There was a total of 479 patients in our final study population, of which 379 (79.1%) were treated at an adult center and 100 (20.9%) were treated at a pediatric center. Patients treated at an adult center had a 10 year overall survival of 86% compared to 85% for patients treated at a pediatric center (<italic>P</italic> = 0.31). Race and poverty were not significantly associated with death. Patients with nasopharyngeal carcinoma (OR = 7.38; 95% CI = 2.30–23.75) and 'other carcinomas'<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25326-sec-0001" sec-type="section"> <title>Background</title> <p>The type of treatment center where 15–21‐year‐old adolescent and young adult (AYA) patients with rare pediatric tumors achieve their best clinical outcome is unknown.</p> </sec> <sec id="pbc25326-sec-0002" sec-type="section"> <title>Procedure</title> <p>We performed a retrospective analysis using the Georgia Cancer Registry (GCR) of 15–21‐year old patients with a malignant, rare pediatric tumor diagnosed during the period from 2000–2009. Patients were identified as being treated at one of five Georgia pediatric cancer centers or at an adult center. Data were analyzed for 10 year overall survival, patient characteristics associated with death, and patient characteristics present at diagnosis associated with choice of treatment center.</p> </sec> <sec id="pbc25326-sec-0003" sec-type="section"> <title>Results</title> <p>There was a total of 479 patients in our final study population, of which 379 (79.1%) were treated at an adult center and 100 (20.9%) were treated at a pediatric center. Patients treated at an adult center had a 10 year overall survival of 86% compared to 85% for patients treated at a pediatric center (<italic>P</italic> = 0.31). Race and poverty were not significantly associated with death. Patients with nasopharyngeal carcinoma (OR = 7.38; 95% CI = 2.30–23.75) and 'other carcinomas' (OR = 2.64; 95% CI = 1.25–5.60) were more likely to be treated at a pediatric center. Patients with higher‐stage disease (OR = 4.24; 95% CI = 1.71–10.52) and higher poverty (OR = 2.32; 95% CI = 1.23–4.37) were also more likely to be treated at a pediatric center.</p> </sec> <sec id="pbc25326-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Our data suggest that there is no difference in survival for 15–21‐year old patients with rare pediatric tumors when treated at an adult or pediatric center. Pediatr Blood Cancer 2015;62:456–462. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric blood & cancer. Volume 62:Issue 3(2015:Mar.)
- Journal:
- Pediatric blood & cancer
- Issue:
- Volume 62:Issue 3(2015:Mar.)
- Issue Display:
- Volume 62, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 62
- Issue:
- 3
- Issue Sort Value:
- 2015-0062-0003-0000
- Page Start:
- 456
- Page End:
- 462
- Publication Date:
- 2014-11-12
- 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.25326 ↗
- 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
British Library HMNTS - ELD Digital store - Ingest File:
- 4393.xml