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Therapeutic vulnerability in acute leukemia – EMC2

Therapeutic vulnerability in acute leukemia – EMC2

Home » Funded projects » Therapeutic vulnerability in acute leukemia – EMC2

Acute lymphoblastic leukemia (ALL) is the most common childhood cancer, and ALL-T accounts for 20% of these cancers, peaking at 2-5 years of age. Although this cancer originates in the thymus, it spreads throughout the body and is rapidly lethal without treatment. Current treatments for T-ALL achieve good survival rates of 90% in children, but with serious side effects that impair their long-term quality of life. What’s more, around 50% of adolescents and 60% of adults succumb to T-ALL. In contrast, acute myeloblastic leukemia is more common in adults with a low long-term survival rate, despite intensive high-dose chemotherapy.

The team has previously shown that leukemic stem cells that are spared by current treatment actually depend on their interactions with a niche for survival, revealing a vulnerability that they propose to exploit in order to develop new compounds that prevent this critical interaction. The project involves a multidisciplinary team of researchers working in synergy from bench to bedside at three universities: IRIC-Université de Montréal, MUHC and Université de Sherbrooke, as well as CHU Sainte-Justine.

Principal Investigator

Trang Hoang
Institute for Research in Immunology and Cancer (IRIC)

Co-researchers

Michel Bouvier
Institute for Research in Immunology and Cancer (IRIC)
Kolja Eppert
McGill University Health Centre (MUHC)
Richard Leduc
Sherbrooke University
Marc Therrien
Institute for Research in Immunology and Cancer (IRIC)
Henrique Bittencourt
Sainte-Justine UHC

In a nutshell

Principal Investigator

Trang Hoang

Competitions

EMC2

Status

In progress

Start

08 2018

Scheduled finish

07 2021

Budget

1 500 000 $
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