Professor Stephen Opat |
Research at Monash Haematology
was recognised at the 14th International Conference on Malignant
Lymphoma held in Lugano, Switzerland last week, attended by more than 3000 international
delegates.
The event is the premier
scientific meeting for haematologists, oncologists, radiation oncologists, paediatricians,
pathologists and leading researchers involved in the study and treatment of lymphoma.
Monash clinicians and researchers
had four abstracts including three oral presentations and one poster. A landmark chemotherapy-free study in follicular and aggressive B cell lymphoma
was one of only three abstracts selected for presentation at the plenary
session. The study examined the activity of Tazemetostat, a first-in-class,
oral inhibitor of EZH2, an enzyme involved in reading of the DNA code.
“The long strands of DNA in the cells are tightly
coiled around proteins called histones. However, DNA needs to be uncoiled to be
read by the cell’s machinery. The EZH2 enzyme adds a mark to the histones which
stops the DNA from uncoiling. The enzyme can be abnormally activated in several
cancers including lymphoma, breast, prostate, melanoma, and bladder cancer.
Tazemetostat can inhibit the EZH2 enzyme thus enabling the cells to read the
DNA once more”, Professor Opat said.
Responses were seen in 92% of patients with
relapsed follicular lymphoma and 29% with relapsed aggressive B cell lymphoma
who had an abnormally activated EZH2. The Tazemetostat tablets were extremely
well tolerated with few side effects.
Other presentations highlighted the clinical activity
of ‘BGB-3111’, a next generation inhibitor of the Bruton Tyrosine Kinase enzyme
in patients with chronic lymphocytic leukaemia and Waldenström’s
macroglobulinemia.
Haematology Research is conducting further
studies with these agents in the Monash Health Translation Precinct Clinical
Trial Facility.
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