Grants Search Results

The most common childhood cancer, acute lymphoblastic leukemia is a cancer of the bone marrow. Exciting new research shows that healthy normal bone marrow cells can protect leukemia cells from cancer drugs. Dr. Mullen's research aims to find ways to prevent normal marrow cells from protecting leukemia cells and thus make cancer drugs more effective.

Langerhans cell histiocytosis (LCH) is a very rare type of neoplasm of the blood that has not been well investigated. It has been traditionally excluded from the major cooperative research groups, and thus considered an orphan disease. However, LCH affects many children. This consortium uses a uniform treatment while investigating the biology of the disease to seek for better therapeutic targets. Awarded at Dana-Farber Cancer Institute and transferred to St. Jude Children's Research Hospital. Funds administered by St. Jude Children's Research Hospital.

This institution is a member of a research consortium which is being funded by St. Baldrick's: North American Consortium for Histiocytosis (NACHO). For a description of this project, see the consortium grant made to the lead institution: St. Jude Children's Research Hospital, Memphis, TN.

This institution is a member of a research consortium which is being funded by St. Baldrick's: North American Consortium for Histiocytosis (NACHO). For a description of this project, see the consortium grant made to the lead institution: St. Jude Children's Research Hospital, Memphis, TN.

This institution is a member of a research consortium which is being funded by St. Baldrick's: North American Consortium for Histiocytosis (NACHO). For a description of this project, see the consortium grant made to the lead institution: St. Jude Children's Research Hospital, Memphis, TN.

This institution is a member of a research consortium which is being funded by St. Baldrick's: North American Consortium for Histiocytosis (NACHO). For a description of this project, see the consortium grant made to the lead institution: St. Jude Children's Research Hospital, Memphis, TN.

This institution is a member of a research consortium which is being funded by St. Baldrick's: North American Consortium for Histiocytosis (NACHO). For a description of this project, see the consortium grant made to the lead institution: St. Jude Children's Research Hospital, Memphis, TN.

This institution is a member of a research consortium which is being funded by St. Baldrick's: North American Consortium for Histiocytosis (NACHO). For a description of this project, see the consortium grant made to the lead institution: St. Jude Children's Research Hospital, Memphis, TN.

This institution is a member of a research consortium which is being funded by St. Baldrick's: North American Consortium for Histiocytosis (NACHO). For a description of this project, see the consortium grant made to the lead institution: St. Jude Children's Research Hospital, Memphis, TN.

This institution is a member of a research consortium which is being funded by St. Baldrick's: North American Consortium for Histiocytosis (NACHO). For a description of this project, see the consortium grant made to the lead institution: St. Jude Children's Research Hospital, Memphis, TN.

This institution is a member of a research consortium which is being funded by St. Baldrick's: North American Consortium for Histiocytosis (NACHO). For a description of this project, see the consortium grant made to the lead institution: St. Jude Children's Research Hospital, Memphis, TN.

This institution is a member of a research consortium which is being funded by St. Baldrick's: North American Consortium for Histiocytosis (NACHO). For a description of this project, see the consortium grant made to the lead institution: St. Jude Children's Research Hospital, Memphis, TN.

This institution is a member of a research consortium which is being funded by St. Baldrick's: North American Consortium for Histiocytosis (NACHO). For a description of this project, see the consortium grant made to the lead institution: St. Jude Children's Research Hospital, Memphis, TN.

Based on progress to date, Dr. Shand was awarded new grants in 2017 and 2018 to fund additional years of this Scholar award. Leukemia is a blood cancer that kills more children than any other cancer. Dr. Shand's work is based on the belief that leukemia behaves like some infections do, by tricking our body into thinking it's OK to set up shop there. Dr. Shand is studying how leukemia can send these “trick signals” to the part of our body that fights off infections, the immune system. This research aims to understand how these trick signals work, with the goal of turning them off so that the immune system can be used to cure leukemia. This grant is generously supported by Micaela's Army Foundation, a St. Baldrick's partner which was founded in loving memory of Micaela White who fiercely fought Acute Myeloid Leukemia at the age of 18. Their mission is to raise money to help fund cancer research, education, awareness, and patient support for the cancers that affect children and their families.

Rhabdomyosarcoma is the most common soft tissue sarcoma in children. Dr. Shern's group recently discovered that mutations in 10 genes drive this disease. This research grant is determining whether these mutations can be used as markers of prognosis or response to therapy. Dr. Shern hopes to develop a tool that can be used to better detect and treat rhabdomyosarcoma. If successful, the developed tool can immediately be integrated into clinical trials to improve the current therapy. This grant is made with generous support from the PFP Fund for Cancer Research, a St. Baldrick's Hero Fund created in memory of Peyton Arens and honors his fighting spirit by supporting research that will bring about cures and less toxic treatments.

Based on progress to date, Dr. Zhang was awarded new grants in 2017 and 2018 to fund additional years of this International Scholar award. Though cure rates have improved dramatically, geographic inequities in childhood acute lymphoblastic leukemia (ALL) therapy remain evident between developed vs. low-middle income countries. In China, about 7,700 newly-diagnosed children with ALL every year receive therapy thanks to the coverage provided by a special national health insurance scheme established in 2010. With the drastic increase in access to clinical care, the challenge is now shifting from remedying the inability to pay for ALL therapy to delivering better therapy and improving outcome. Dr. Zhang is working to bring improved therapy to China. This represents an unprecedented opportunity for translational research of childhood ALL in China, with potential impacts for a large number of patients.

Based on progress to date, Dr. Zhang was awarded new grants in 2017 and 2018 to fund additional years of this International Scholar award. Though cure rates have improved dramatically, geographic inequities in childhood acute lymphoblastic leukemia (ALL) therapy remain evident between developed vs. low-middle income countries. In China, about 7,700 newly-diagnosed children with ALL every year receive therapy thanks to the coverage provided by a special national health insurance scheme established in 2010. With the drastic increase in access to clinical care, the challenge is now shifting from remedying the inability to pay for ALL therapy to delivering better therapy and improving outcome. Dr. Zhang is working to bring improved therapy to China. This represents an unprecedented opportunity for translational research of childhood ALL in China, with potential impacts for a large number of patients.

This grant helps provide necessary resources to increase enrollment in early phase clinical trials for neuroblastoma patients, and support the development of a new MIBG Therapy program to treat neuroblastoma.

This grant funds a Clinical Research Associate to ensure that more kids can be treated on clinical trials, often their best hope for a cure.

Leukemia is the most common childhood cancer. Some types of leukemia cells have abnormal genetic material. One of these abnormalities is known to affect the CALM protein, which is essential for the cell to obtain iron from the body that is necessary for cell growth. Dr. Heath believes that leukemias with the abnormal CALM-AF10 protein will not have enough iron and by reducing the amount of iron available to them, the leukemia cells may be affected. This research project attempts to prove that these two mutations can cooperate to form leukemia. Dr. Heath also attempts to show that mutations of WT1 cause cells to function abnormally, which contribute to the development of leukemia. Preliminary work shows that cells with WT1 mutations grow faster and more aggressively. The first model to study the cooperation of FLT3/ITD and WT1 mutations has been created. Ultimately, if WT1 mutations are shown to contribute to the formation of leukemia, the development of a drug that interferes with WT1 could improve cure rates in patients with AML.