The Children'sOncology Group (COG) is a new multidisciplinaryclinicaltrialsgroup resultingfrom the unificationof the four pediatriccooperativegroups. It is thelargestchildhoodcancer research organization in the worldand encompasses approximately238 pediatriccancer programs as clinicaltrial sites throughoutall of NorthAmerica, Australia, and several institutionsin Europe. It is exclusivelywell poisedto translate basic biologystudies intoclinicalinvestigationsand to develop translationalapproaches through human proofof principle,toxicity assessment, identificationof efficacy, and ultimately,incorporationintoestablished treatmentsto improve outcome and/or decrease toxicity.COG representsthe legacyof four groups,the oldest of which existedfor nearly 50 years. Currently, 48,259 patients accruedto clinicaltrialsare in active follow-up;over 2,500,000 person years of life have been saved. Although childhoodcancer mortality has decreased by 50% in the lasttwo decades and by 25% inthe past decade, nearly 2,500 childrenand adolescents die from cancer annuallyinthe U.S. alone. The majorityof these deaths can be attributedto specificpediatric cancersfor which new therapeuticapproachesmust be devised. Improvementin the cure ratesfor these high-riskcancers is more likelyto emerge as a result of the identificationof biologicfeatures whichpredict resistanceand, more importantly, by the identificationof new anti-cancer agents with novel mechanisms of action,whose efficacy might be predictedon the basis of specificunique molecular abnormalitiesdetected in cancer cells. COG is also uniquelyable to establishfor the first time a North America-wide population-basedregistry of childhoodcancerto investigate,utilizingcase control studies, potentialepidemiologicassociations,includinggenetic alterationsand ultimatelyinteractions of genes with the environment.COG, through a series of hypothesis-drivenresearch studies,seeks to maximize cure rates for children with cancer; to achieve an expanded understandingof tumor and hostbiology;to elucidatenew therapeutic strategies and to build on the concept of risk-adjustedtherapy; and to reduce treatment-related toxicityand morbidity, thereby optimize quality of life and survival.The proposed research is aimed at reducingdeaths from childhood cancer by 20% and increasing 5-year disease-free survival (cure) rates to >85% duringthe studyperiod.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Cooperative Clinical Research--Cooperative Agreements (U10)
Project #
3U10CA098543-05S1
Application #
7406216
Study Section
Subcommittee G - Education (NCI)
Program Officer
Smith, Malcolm M
Project Start
2003-07-07
Project End
2008-02-29
Budget Start
2007-03-01
Budget End
2008-02-29
Support Year
5
Fiscal Year
2007
Total Cost
$2,049,520
Indirect Cost
Name
National Childhood Cancer Foundation
Department
Type
DUNS #
624124301
City
Arcadia
State
CA
Country
United States
Zip Code
91006
Mullen, Elizabeth A; Chi, Yueh-Yun; Hibbitts, Emily et al. (2018) Impact of Surveillance Imaging Modality on Survival After Recurrence in Patients With Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group. J Clin Oncol :JCO1800076
Laetsch, Theodore W; Roy, Angshumoy; Xu, Lin et al. (2018) Undifferentiated Sarcomas in Children Harbor Clinically Relevant Oncogenic Fusions and Gene Copy-Number Alterations: A Report from the Children's Oncology Group. Clin Cancer Res 24:3888-3897
Koster, Roelof; Panagiotou, Orestis A; Wheeler, William A et al. (2018) Genome-wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients. Int J Cancer 142:1594-1601
Barredo, Julio C; Hastings, Caroline; Lu, Xiamin et al. (2018) Isolated late testicular relapse of B-cell acute lymphoblastic leukemia treated with intensive systemic chemotherapy and response-based testicular radiation: A Children's Oncology Group study. Pediatr Blood Cancer 65:e26928
Marks, Lianna J; Pei, Qinglin; Bush, Rizvan et al. (2018) Outcomes in intermediate-risk pediatric lymphocyte-predominant Hodgkin lymphoma: A report from the Children's Oncology Group. Pediatr Blood Cancer 65:e27375
Dicken, Bryan J; Billmire, Deborah F; Krailo, Mark et al. (2018) Gonadal dysgenesis is associated with worse outcomes in patients with ovarian nondysgerminomatous tumors: A report of the Children's Oncology Group AGCT 0132 study. Pediatr Blood Cancer 65:
Hawkins, Douglas S; Chi, Yueh-Yun; Anderson, James R et al. (2018) Addition of Vincristine and Irinotecan to Vincristine, Dactinomycin, and Cyclophosphamide Does Not Improve Outcome for Intermediate-Risk Rhabdomyosarcoma: A Report From the Children's Oncology Group. J Clin Oncol 36:2770-2777
Williams, Lindsay A; Pankratz, Nathan; Lane, John et al. (2018) Klinefelter syndrome in males with germ cell tumors: A report from the Children's Oncology Group. Cancer 124:3900-3908
Rajbhandari, Presha; Lopez, Gonzalo; Capdevila, Claudia et al. (2018) Cross-Cohort Analysis Identifies a TEAD4-MYCN Positive Feedback Loop as the Core Regulatory Element of High-Risk Neuroblastoma. Cancer Discov 8:582-599
Ehrlich, Peter F (2018) Reply to: Synoptic operative reports for quality improvement in pediatric cancer care: Surgical protocol violations in children with renal tumors provides an opportunity to improve pediatric cancer care: A report from the Children's Oncology Group. Pediatr Blood Cancer 65:e27277

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