Publication authors Prof Stephen Opat, Dr Sumita Ratnasingham and Assoc Prof Jake Shortt at the ASH Annual Meeting 3 December 2016 |
In a world-first, a Monash University study has shown an
anti-myeloma drug to be an effective treatment against a range of autoimmune
diseases affecting the blood.
Thrombotic thrombocytopenic purpura (TPP) is one such
disease—a rare blood disorder characterised by clotting in small blood vessels.
TPP causes microscopic clots to form throughout the body that can damage organs
including the kidneys, heart and brain.
“At Monash, we were the first ever to use bortezomib (an
anti-myeloma drug) in a patient with TPP,” said lead researcher and Monash
Health haematologist Associate Professor Jake Shortt.
“Further to the patient’s full recovery and our New
England Journal paper about this in 2013, we have successfully used
bortezomib in a number of patients with a range of nasty autoimmune diseases
affecting the blood.”
Presented as a case series, Associate Professor Shortt’s
research was published this week in the inaugural issue of Blood Advances,
a new peer-reviewed journal published by the American Society of Hematology and
the first journal to join the Blood family in 70 years.
“If you consider that leukaemia and lymphoma are cancers of
the immune system and that autoimmune disease is caused by an overactive immune
system, you can rationalise that anti-lymphoma drugs could be good for
autoimmune disease,” said Associate Professor Shortt, who is also Head of
Haematology Research at the Monash Health Translation Precinct.
Associate Professor Shortt said that the subsequent use of
bortezomib in ten Monash Health patients was carried out ‘off label’ through
compassionate access—a real credit to Monash Health’s attitude towards drug
availability for patients in need.
“Although our paper is a case series rather than a clinical
trial, we have observed high response rates with minimal toxicity,” said
Associate Professor Shortt.
Associate Professor Shortt presented an abstract of this
work at last year’s American Society of Hematology annual meeting, and it was
subsequently listed in the Cleveland Clinics top 10 most compelling 2015 benign
haematology abstracts.
The article published in Blood Advances was also distributed to 27,000 delegates at the American Society of Hematology's Annual Meeting in San Diego last weekend.
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