Genomic medicine is the use of information from your DNA to inform patient diagnosis and care. Clinical genomics is a rapidly-changing field. The technologies that are used to read and analyse a genome (genome sequencing machines) have changed dramatically in the last decade, making genomic testing much more accessible to individuals and to the health system. Knowledge of the human genome is far from complete, but there are already many uses for genetic and genomic information in the clinic.
Genomic information is expected to have the most impact in:
- Diagnosing and understanding rare and inherited disease;
- Profiling individuals’ tumours to guide treatment (precision medicine);
- Providing information about an individual’s risk of developing disease or their likely response to treatment (health management).
Rare genetic disease
Characterising and diagnosing inherited disease
Every baby born in Australia is offered screening for approximately 30 genetic conditions (the Guthrie test) and more than 300 tests for genetic disorders are available through the healthcare system.
Clinicians worldwide are beginning to embrace genome sequencing to search for variants implicated in undiagnosed genetic diseases and using this information to guide treatment. In one of the most dramatic cases, a young boy underwent a risky, but seemingly successful, bone marrow transplant that was proposed in response to molecular data.
The Garvan Institute launched Australia’s first clinical whole genome sequencing service, Genome.One in 2016. Garvan partnered with Australian Clinical Labs in 2018 to continue and expand access to this important service for Australians living with rare and genetic conditions.
Cancer genomic medicine
Stratifying cancer for earlier detection and better treatment
A major focus of genomic medicine is cancer diagnosis and therapy. Clinicians are beginning to use genomic information to predict how a person’s cancer will respond to drug therapy or surgery. In some cases, clinicians will profile the DNA and RNA of tumour cells to guide the use of existing treatments or focus on more targeted treatments.
As a fundamentally genetic disease, cancer risk can be inherited. Understanding genetic variation enables more effective and earlier detection, which in turn leads to a better chance for treatment, intervention or cure.
The Australian Genomic Cancer Medicine Program, led by the Head of Garvan’s Cancer Division and Director of The Kinghorn Cancer Centre, Professor David Thomas, is a research program dedicated to applying genomics to the understanding, early detection, prevention and management of cancer. This program was originally established as part of the Sydney Genomics Collaborative, a $24 million, four-year investment by the NSW State Government in using genetic technologies to improve patient outcomes.
Health management: understanding disease risk and predicting drug response
The application of genomic medicine is not limited to typically genetic conditions. All diseases have a genetic component, from inherited conditions to complex diseases such as cancer and diabetes. Different people also react differently to parasites, viruses and bacteria according to the information encoded in their genome.
Beyond diagnosis and guiding patient management, the major value for genomics in health is expected to be in:
- understanding an individual’s disease risk
- detecting disease early, and, ultimately, preventing disease.
Researchers are identifying a broad range of variants – across the genome – that are clinically useful.
Individuals’ genetic differences are also thought to be responsible for up to 80% of adverse reactions to drugs and genetic tests for variants involved in drug metabolism. Comprehensive profiles of an individual’s genetic data, integrated with common clinical markers, are expected to provide new insights into disease.