Pediatric Malignancies: Inventory of DCEG Research

A clinical study to learn more about how genetic and environmental factors contribute to the development of atypical spitzoid tumors. Results from this study could improve prevention and treatment.

IIB research into Burkitt Lymphoma (BL) aims to improve understanding of the distribution of BL in different populations, the markers markers of P. falciparum and EBV infections that are associated with BL, and the genetic factors that influence risk of BL.

Childhood leukemia is the most common type of childhood cancer, and its etiology is not well understood. DCEG researchers are investigating novel molecular biomarkers as well as potential risk factors including inherited, medical, and environmental exposures.

DCEG is evaluating PFAS exposure in the Finnish Maternity Cohort to explore its relationship with acute lymphoblastic leukemia risk in children.

A population-based case-control study of childhood leukemia in the San Francisco Bay area and the agricultural Central Valley

A study investigating the association of childhood leukemia with natural background radiation exposure

Pediatric Proton and Photon Therapy Comparison Cohort is a multi-center retrospective cohort to investigate second cancers after photon versus proton radiotherapy for pediatric cancer.

DCEG investigators are studying inherited genetic variation to identify regions in the genome associated with increased risk of Ewing Sarcoma (EwS), a pediatric bone and soft tissue tumor. The overall goal of the study is to expand our understanding of EwS etiology and provide insight into improved treatment and potentially preventative measures to reduce the overall burden of EwS.

Children and adults with mutations in DICER1 are at increased risk for a variety of cancers, including pleuropulmonary blastoma (PPB), a rare tumor of the lung. The DICER1 Natural History Study is an observational study of children with PPB and other tumors and their families.

The Fanconi Anemia Cancer Screening Study seeks to improve cancer screening in people with Fanconi anemia (FA), the most common Inherited Bone Marrow Failure Syndrome (IBMFS). The study is enrolling new participants.

Genetic studies of osteosarcoma to better understand the role that genetic variation plays in risk and patient outcomes, and to identify new genes or genomic regions that may be important in osteosarcoma pathogenesis.

A study of inherited bone marrow failure syndromes (IBMFS), a group of rare genetic blood disorders that include Fanconi Anemia, Dyskeratosis Congenita, Diamond-Blackfan Anemia, Shwachman-Diamond Syndrome, Severe Congenital Neutropenia, Amegakaryocytic Thrombocytopenia, and Thrombocytopenia Absent Radii.

A clinical study and multi-institutional collaboration for research on Li-Fraumeni Syndrome (LFS). The NCI has evaluated families with LFS since the syndrome was first recognized in 1969. DCEG is now expanding this research through a clinical study and participation in a multi-institutional collaboration.

A RASopathy syndrome is a condition or disorder caused by changes in genes that send signals across the Ras/mitogen-activated protein kinase (Ras/MAPK) pathway. The RASopathies Study is a clinical study that aims to better understand the development of tumors in patients with a RASopathy syndrome.

Studies of secondary glioma, meningioma, thyroid, breast, soft tissue, bone, and skin cancers among more than 14,000 five-year survivors of childhood cancer diagnosed between 1970 and 1986.

A study of long-term cancer risk in survivors of retinoblastoma, a cancer that forms in the tissues of the retina.