Vancouver Sun

Genetic tests could spare kids adverse effects of cancer drugs

Screening would allow parents, doctors to choose safer, personaliz­ed treatment

- CAMILLE BAINS

A scientist who developed a lab test to predict whether children with cancer are susceptibl­e to potentiall­y life-threatenin­g sideeffect­s from three chemothera­py drugs is now focusing on five other medication­s so parents and doctors can discuss safer, personaliz­ed treatment.

Bruce Carleton, director of the Pharmaceut­ical Outcomes Programme at B.C. Children’s Hospital, said adverse reactions linked to the five medication­s include bone disease, pancreatit­is, anaphylaxi­s, nerve damage in the limbs, and inflammati­on of the mucous membranes, including those that may prevent patients from swallowing.

The four-year project is part of a Genome Canada study that will include the creation of a publicly available genetic database that could be accessed by researcher­s around the world, Carleton said.

He and his colleague, Colin Ross, have already identified genetic variants linked to three commonly prescribed drugs that cause heart failure, hearing loss or suppressio­n of bone marrow, which reduces the body’s ability to fight infections.

For the last two years, cancer patients Carleton has seen at a B.C. Children’s Hospital clinic have been given a genetic test to determine if they are at risk for reactions.

Carleton said he would like children at all cancer centres in Canada to be geneticall­y tested for adverse reactions to the potent medication­s.

They include anthracycl­ine, which plays a role in dramatical­ly improving survivabil­ity rates of many cancers, but also causes heart failure in some cases.

“I think that we can begin the conversati­ons before treatment begins about what the adverse effect means, instead of waiting for it to occur and saying, ‘Well, this happens sometimes,’” Carleton said. “Often, parents say to me that the adverse effects of cancer chemothera­py were harder for them to manage and deal with than the survival questions because they ’re not prepared for it.”

Their research includes analysis of more than 6,100 DNA samples as they work to discover genetic susceptibi­lity to side-effects from the five drugs in the expanding field of pharmacoge­nomics.

Genetic testing provides oncologist­s with informatio­n that can help them weigh the risks and benefits of some treatment as they consider options that may include lowering the dosage of a toxic drug or providing an alternativ­e therapy, he said.

“Sometimes the results are reassuring, that if you need to exceed the dose, the likelihood of toxicity is fairly low compared to other children,” said Carleton, who is also a professor of pediatrics at the University of British Columbia.

Parents need to be part of the treatment discussion, he said.

“Coming up with a way for them to better understand what their child’s risk is allows them to say, ‘Survival isn’t the only thing. I also want to know about harm,’ ” he said.

Bethany Prokuda’s four-year-old daughter Rory Nichols was diagnosed with a tumour at the tip of her tail bone about three weeks after she was born.

She said genetic testing soon after Rory’s first birthday revealed she was on a chemothera­py drug that put her at over 80 per cent risk of hearing loss related to F, S and “th” sounds in words such as Friday, Saturday and Thursday.

Prokuda, a registered nurse, said she decided to switch her daughter to a different medication after discussing options with Rory’s oncologist.

“If they can give them an answer and maybe be able to tailor the therapies so that these kids do have good outcomes, it’s absolutely essential,” she said of genetic tests.

Prokuda said she began speech therapy for Rory, who is currently doing well while trying to keep up with her eight-year-old sister Avery.

“She’s definitely progressed better from where it was. From age two to age four she’s caught up on a lot of those sounds,” Prokuda said.

“She’s singing along to music, she’s copying her big sister reading books, it’s really good.”

Dr. Rod Rassekh, who has treated Rory, along with her primary oncologist, said the genetic test “really helped spare a lot of her hearing.”

Rassekh said the parents of one of his patients who was tested decided they wanted their child taken off a drug that would cause heart problems, even if that put the youngster at slightly higher risk of relapse.

Coming up with a way for them to better understand what their child’s risk is allows them to say, ‘Survival isn’t the only thing. I also want to know about harm.’

“So that’s what I think this test does, is facilitate­s really good discussion­s with families, where they can be empowered to make decisions.”

Rassekh said all oncologist­s at B.C. Children’s Hospital now routinely use genetic testing, even though they were initially concerned about what they and parents would do with the informatio­n it provided.

“What it’s allowed us to do is actually have very open discussion­s about side-effects and consider parents’ values and what they deem important. What they think is high risk may not be what I think is high risk as a doctor.”

 ?? THE CANADIAN PRESS ?? Four-year-old Rory Nichols had a genetic test that determined she was at risk for hearing loss from a chemothera­py drug, so her mother and doctor decided to switch her to another medication.
THE CANADIAN PRESS Four-year-old Rory Nichols had a genetic test that determined she was at risk for hearing loss from a chemothera­py drug, so her mother and doctor decided to switch her to another medication.

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