Grants Search Results

Pediatric Philadelphia Chromosome positive (Ph+) acute lymphoblastic leukemia (ALL) has a poor prognosis despite the introduction of Ph+ targeted drugs (TKIs). And for patients that fail to respond or relapse after TKIs, the prognosis remains grim. Dr. Cohen is studying why pediatric Ph+ ALL patients relapse (or fail to respond) to TKI treatment. Dr. Cohen has shown in early studies that combinations of TKIs and another new class of drugs can overcome TKI resistance. Because many of the drugs Dr. Cohen and his team are testing are commercially available, promising data from their research may move into future clinical trials.

Based on progress to date, Dr. Ney was awarded a new grant in 2018 to fund an additional year of this Fellow award. Many cancers include groups of cells that are relatively inactive, meaning that they divide less frequently than other cells and use fewer nutrients from their environment. This inactivity often makes these cells less susceptible to chemotherapy because these cells do not take in chemotherapy drugs due to their slow growth. As a result, these cells can remain present after treatment, potentially leading to disease recurrence. Dr. Ney is studying these inactive cells and their behavior, to more fully understand cancer and how to better treat it.

The initial grant was made with generous support from Tough Like Ike, a St. Baldrick's partner which was created in honor of cancer fighter Issac "Ike" Yarmon. The organization raises awareness and funds for leukemia and childhood cancer research.

This additional award is named for Ben's Green Drakkoman Fund, a St. Baldrick's Hero Fund created in memory of Ben Stowell who battled an aggressive form of osteosarcoma yet lived life with courage and an inspiring determination to survive. The fund is named after the superhero he created to help him better understand his body's fight against cancer.

Langerhans cell histiocytosis (LCH) is a rare cancer of the immune cells that can cause a wide range of symptoms, ranging from a rash to lethal multi-organ disease. Dr. Zinn hypothesizes that a patient's symptoms are determined by a combination of the patient's specific mutation and the specific immune cell that becomes mutated. Dr. Zinn is investigating the causes of LCH in order to develop the most effective and safe therapies for each patient.

Based on progress to date, Dr. Huang was awarded a new grant in 2018 to fund an additional year of this Fellow award. Cure rates for Acute myeloid leukemia (AML) are poor and current therapies are toxic. Dr. Huang is using accurate models of AML to test novel agents that target cancer specific dependences. The overall goal of Dr. Huang's research is to develop new therapeutic strategies in AML to enhance efficacy and reduce toxicity. This research will inform efforts to develop novel treatment combinations in children with AML.

Based on progress to date, Dr. Sinha was awarded a new grant in 2018 to fund an additional year of this Fellow award. Myelodysplastic syndrome is a rare disease that affects the stem cells in the bone marrow, which causes decreased blood counts. It is also known to be a precursor to acute myeloid leukemia. Cellular mutations are present in majority of these cases, however the mechanisms of development of these mutations are still not clear. Dr. Sinha is studying these interactions, in order to identify new prognostic factors and therapeutic options for these patients. Awarded at Albert Einstein College of Medicine and transferred to University of Oklahoma Health and Science Center.

Children with aggressive leukemia frequently require a bone marrow transplant to achieve a cure. Some children have a small number of leukemia cells remaining before receiving a bone marrow transplant, which makes it very likely that their leukemia will recur. Dr. Taraseviciute, the Team Abby St. Baldrick's Fellow, is studying the power of the immune system to fight any remaining leukemia cells after bone marrow transplantation. To do this, Dr. Taraseviciute and her team are making T cells (a special type of immune cell) that can recognize and eliminate leukemia cells to provide a chance for a cure for children who have already received a bone marrow transplant.

This grant is generously supported by TEAM ABBY Gives, a St. Baldrick's Hero Fund. Abby was diagnosed with Pre-B ALL when she was almost five years old. She had a successful bone marrow transplant, but battle battled graft vs. host disease (GVHD) for years. Abby and her treatment team worked hard over many years to keep the GVHD in check. Sadly, Abby passed away on October 19, 2021. This fund unites the incredible support of family and friends in Abby's memory and inspires others to join the fight for cures and better treatments.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Pediatric LEukemiA Precision-based Therapy (LEAP) Consortium. For a description of this project, see the consortium grant made to the lead institution: Dana-Farber Cancer Institute, Boston, MA.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Pediatric LEukemiA Precision-based Therapy (LEAP) Consortium. For a description of this project, see the consortium grant made to the lead institution: Dana-Farber Cancer Institute, Boston, MA.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Pediatric LEukemiA Precision-based Therapy (LEAP) Consortium. For a description of this project, see the consortium grant made to the lead institution: Dana-Farber Cancer Institute, Boston, MA.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Pediatric LEukemiA Precision-based Therapy (LEAP) Consortium. For a description of this project, see the consortium grant made to the lead institution: Dana-Farber Cancer Institute, Boston, MA.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Pediatric LEukemiA Precision-based Therapy (LEAP) Consortium. For a description of this project, see the consortium grant made to the lead institution: Dana-Farber Cancer Institute, Boston, MA.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Pediatric LEukemiA Precision-based Therapy (LEAP) Consortium. For a description of this project, see the consortium grant made to the lead institution: Dana-Farber Cancer Institute, Boston, MA.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Pediatric LEukemiA Precision-based Therapy (LEAP) Consortium. For a description of this project, see the consortium grant made to the lead institution: Dana-Farber Cancer Institute, Boston, MA.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Pediatric LEukemiA Precision-based Therapy (LEAP) Consortium. For a description of this project, see the consortium grant made to the lead institution: Dana-Farber Cancer Institute, Boston, MA.

This consortium is conducting the first multi-institutional, genomics-based precision medicine trial for children with relapsed, refractory, and very high-risk leukemias. They are deploying new technologies to sequence all currently known cancer-promoting genes in an individual child's leukemia. Next, guided by a multi-disciplinary group of leukemia experts, they will make treatment recommendations based upon the genomic findings in the child's leukemia and the availability of a relevant targeted drugs for children. Results from this project will define the types and frequency of specific mutations in children with relapsed/refractory leukemia, and assess the impact of the treatment recommendations on their clinical care. The consortium will also perform laboratory-based studies to determine the response to therapy in lab models derived from the patient's leukemia cells, to identify new drug targets for these children. Data generated in this proposal will inform future genomically-based targeted therapy trials for children with leukemia with the long-term goal of precise, safe, and more efficacious therapies for children with these diseases. Funds administered by Dana-Farber Cancer Institute.

This grant is named for Hannah’s Heroes, a Hero Fund established to honor Hannah Meeson. At age 6 she was diagnosed with anaplastic medulloblastoma. After a relapse and additional treatment, Hannah currently shows no evidence of disease. Throughout her treatments, Hannah never complained and remained positive and happy. This fund pays tribute to her fight by raising awareness and funding for all childhood cancers because kids like Hannah “are worth fighting for.”

This institution is a member of a research consortium which is being funded by St. Baldrick's: Treehouse Childhood Cancer Initiative. For a description of this project, see the consortium grant made to the lead institution: University of California Santa Cruz, Santa Cruz, CA.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Treehouse Childhood Cancer Initiative. For a description of this project, see the consortium grant made to the lead institution: University of California Santa Cruz, Santa Cruz, CA.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Treehouse Childhood Cancer Initiative. For a description of this project, see the consortium grant made to the lead institution: University of California Santa Cruz, Santa Cruz, CA.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Treehouse Childhood Cancer Initiative. For a description of this project, see the consortium grant made to the lead institution: University of California Santa Cruz, Santa Cruz, CA.

This institution is a member of a research consortium which is being funded by St. Baldrick's: Treehouse Childhood Cancer Initiative. For a description of this project, see the consortium grant made to the lead institution: University of California Santa Cruz, Santa Cruz, CA.