A summary of the osteosarcoma banking efforts: A report from the Children's Oncology Group and the QuadW Foundation. Issue 3 (8th December 2014)
- Record Type:
- Journal Article
- Title:
- A summary of the osteosarcoma banking efforts: A report from the Children's Oncology Group and the QuadW Foundation. Issue 3 (8th December 2014)
- Main Title:
- A summary of the osteosarcoma banking efforts: A report from the Children's Oncology Group and the QuadW Foundation
- Authors:
- Glover, Jason
Krailo, Mark
Tello, Tanya
Marina, Neyssa
Janeway, Katherine
Barkauskas, Don
Fan, Timothy M.
Gorlick, Richard
Khanna, Chand
the COG Osteosarcoma Biology Group - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25346-sec-0001" sec-type="section"> <title>Background</title> <p>Survival rates of patients with osteosarcoma have remained stagnant over the last thirty years. Better understanding of biology, new therapeutics, and improved biomarkers are needed. The Children's Oncology Group (COG) addressed this need by developing one of the largest osteosarcoma biorepositories ever, containing over 15, 000 tumor and tissue samples from over 1, 500 patients.</p> </sec> <sec id="pbc25346-sec-0002" sec-type="section"> <title>Procedure</title> <p>The biology study P9851 and the banking study AOST06B1 has enrolled 1, 787 patients (as of September, 2013). Clinical information was lacking on 510 patients on P9851, who were not enrolled on a concurrent therapeutic trial. The value of these specimens was diminished. The lack of statistical support available for biology projects slowed the analysis of several critical studies. The QuadW Foundation, CureSearch, and the COG formed the Childhood Sarcoma Biostatistics and Annotation Office (CSBAO) to provide the infrastructure and address these needs by linking clinically annotated patient data to archived tissue samples and to develop biostatistical support for childhood sarcoma research.</p> </sec> <sec id="pbc25346-sec-0003" sec-type="section"> <title>Results</title> <p>Originally 5.3% of samples from the 510 patients on P9851 not enrolled<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25346-sec-0001" sec-type="section"> <title>Background</title> <p>Survival rates of patients with osteosarcoma have remained stagnant over the last thirty years. Better understanding of biology, new therapeutics, and improved biomarkers are needed. The Children's Oncology Group (COG) addressed this need by developing one of the largest osteosarcoma biorepositories ever, containing over 15, 000 tumor and tissue samples from over 1, 500 patients.</p> </sec> <sec id="pbc25346-sec-0002" sec-type="section"> <title>Procedure</title> <p>The biology study P9851 and the banking study AOST06B1 has enrolled 1, 787 patients (as of September, 2013). Clinical information was lacking on 510 patients on P9851, who were not enrolled on a concurrent therapeutic trial. The value of these specimens was diminished. The lack of statistical support available for biology projects slowed the analysis of several critical studies. The QuadW Foundation, CureSearch, and the COG formed the Childhood Sarcoma Biostatistics and Annotation Office (CSBAO) to provide the infrastructure and address these needs by linking clinically annotated patient data to archived tissue samples and to develop biostatistical support for childhood sarcoma research.</p> </sec> <sec id="pbc25346-sec-0003" sec-type="section"> <title>Results</title> <p>Originally 5.3% of samples from the 510 patients on P9851 not enrolled on a therapeutic study had full clinical annotation. The efforts of the CSBAO have linked clinical annotation to 90.8% of those specimens and provided statistical analyses to several studies that had used COG samples. As a result, 24 biology studies in osteosarcoma have been completed and published in peer‐reviewed journals.</p> </sec> <sec id="pbc25346-sec-0004" sec-type="section"> <title>Conclusions</title> <p>These samples and in‐silico data are available to the research community for basic and translational science projects to improve the biological understanding and treatment of patients affected by osteosarcoma. Pediatr Blood Cancer 2015;62:450–455. © 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:
- 450
- Page End:
- 455
- Publication Date:
- 2014-12-08
- 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.25346 ↗
- 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:
- 4394.xml