Sequencing Offers New Hope for Rare Cancers
Genetic sequencing shows promise for matching people with rare cancers to the right treatments, according to a new clinical trial. Image credit: Walter + Eliza Hall Institute of Medical Research
A cancer’s genetic sequence may be the key to matching people with rare cancers to the right anti-cancer treatments, according to a new clinical trial instigated by patients.
The national trial indicated that genomic profiling of rare cancers – which collectively account for more than 20 per cent of cancer diagnoses in Australia – has the potential to improve a patient’s diagnosis and treatment.
The trial, which will be presented today at the Clinical Oncology Society of Australia Annual Scientific Meeting, was the first of its kind in Australia to be instigated by people affected by rare cancers.
The pilot study was conducted at four centres across Australia, and was led by Walter and Eliza Hall Institute researcher Professor Clare Scott, who is a medical oncologist at the Peter MacCallum Cancer Centre and the Royal Women’s Hospital.
At a glance
Better treatments are needed for people with rare cancers, which collectively cause more cancer deaths in Australia than any single cancer type
A new, patient-driven clinical trial has investigated whether genomic profiling of rare cancers can improve the diagnosis and treatment of people with rare cancers
Genomic profiling provided meaningful information that influences diagnosis and treatment in more than half the trial participants, offering hope for better outcomes for patients
Finding better treatments
A cancer type is considered rare if it affects fewer than 6 people per year per 100,000 people. Despite being individually uncommon, rare cancers collectively account for more than 20 per cent of cancer diagnoses in Australia.
Better approaches to diagnosing and treating rare cancers are urgently needed, said Professor Scott. “More people die from rare cancers in Australia than any other single cancer type. This is because treatments for many rare cancers have not advanced at the same pace as treatments for more common cancers,” she said.
The trial sequenced a panel of genomic markers in participants’ cancers to identify molecular features or mutations in the cancer that could be targeted with existing treatments used in other cancer types with the same characteristics.
“While genomic testing is becoming increasingly used in other cancer types, this is one of the first national studies of its kind in Australia to look at the potential benefits for those with rare cancers,” Professor Scott said.
The NOMINATOR Pilot Study results released today included 36 patients. The two-year study will eventually include 100 patients and will lay the groundwork for other national initiatives looking into genomic profiling across a range of cancer types.
“Australians in this trial came to us after they had exhausted all their options. Using genomic profiling we were able to uncover new information that gave many patients new treatment options – and ultimately, new hope,” said Professor Scott.
“Genomic profiling provided meaningful information that influenced diagnosis and treatment in around half of the participants. 20 percent of those tested got a new treatment plan as a result and 6 percent of participants were given a new diagnosis.”
Professor Phyllis Butow, President, Clinical Oncology Society of Australia said one of the impressive things about the study was that it was driven by Australians directly affected by rare cancers.
“Around 52,000 Australians are diagnosed with rare or less common cancers each year. Those directly affected by the disease helped call for and fund this research, so it’s great to see these initial promising results being presented to cancer experts from across the country.”This article has been republished from materials provided by the Walter and Eliza Hall Institute of Medical Research. Note: material may have been edited for length and content. For further information, please contact the cited source.
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