Medical-scientific program

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Our goals

Cure leukemia at all stages of life

1 Identify predisposing factors for leukemia and provide preventive treatment

2 Understand the heterogeneity of leukemias and develop innovative treatments

3 Explore the mechanisms of treatment resistance

4 Improve patients’ quality of life

Stéphanie CHAMBAUD

Our research areas

Axis 1: MECHANISMS

Basic biology

  • Decipher the heterogeneity of leukemias using a multi-omics approach

  • Identify intrinsic vulnerabilities of leukemias

  • Explore the cellular consequences of therapeutic stresses

Axis 2: MICROENVIRONMENT

Stem cells and microenvironment

  • Study cellular interactions between leukemic cells, stroma, and immune effectors

  • Explore the cellular consequences of therapeutic stresses

Axis 3: PRECISION

Therapeutic agents and combinations

  • Tester des traitements innovants sur des cellules primaires ou sur des modèles pré-cliniques
  • Identifier des combinaisons de traitements prometteuses et valider des biomarqueurs

Axis 4: PREDISPOSITION

Prevention and precision medicine

  • Identify patients with germline predisposing conditions

  • Conduct longitudinal somatic studies

Axis 5: TRIALS

Early clinical trials

  • Develop innovative trials for precision medicine

  • Integrate biological data into clinical trials

Axis 6: CARE

Improving care pathways

  • Implement a post-treatment follow-up program

  • Explore quality of life measures in collaboration with patient associations

Categories of the Institute’s internal call for projects

This category aims to support projects with high potential that are still at an early stage. It provides funding for exploratory work requiring initial support to generate proof-of-concept data, often essential for accessing more conventional funding. This mechanism offers maximum flexibility, with rolling submissions and a budget of up to €30,000 per project.

This category encourages collaboration between multiple teams, notably between basic and clinical research, in order to promote integrated approaches.

This category supports early studies, such as phase I trials or drug repurposing projects, specifically targeting needs not covered by other funding sources.

This category is aimed at projects with high commercialization potential, including possible patent filing or industrial partnership.

Host foundation and founding members

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Frequently Asked Questions

Yes, leukemia is a type of blood cancer. More precisely, it is a cancer that affects the bone marrow, the organ inside the bones responsible for producing blood cells (red blood cells, white blood cells, and platelets).

In leukemia, certain blood cells develop abnormally and uncontrollably. These leukemic cells gradually invade the blood and bone marrow, preventing the normal production of other blood cells. This can lead to symptoms such as fatigue, frequent infections, or bleeding.

  • Basic research: This is research conducted in the laboratory, often on cells, genes, or animals. Its goal is to better understand the biological mechanisms of leukemia.
  • Translational research: This bridges basic research and patient care, applying laboratory findings to develop new treatments or approaches for patients.
  • Clinical research: This research is conducted with patients, often through clinical trials. It allows testing new treatments, drugs, or diagnostic methods to determine if they are effective and safe.

A stem cell is an immature cell capable of transforming into different types of specialized cells in the body. They can be compared to “base cells,” similar to seeds that can grow into different plants.

In the context of blood, we talk about hematopoietic stem cells, which are found in the bone marrow. They have the ability to produce:

  • Red blood cells (which carry oxygen)

  • White blood cells (which defend against infections)

  • Platelets (which help blood clot)

These cells play an essential role, particularly in the treatment of certain leukemias, such as bone marrow transplantation, which involves replacing diseased cells with healthy cells from a donor.