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Is there a cost to convenience? Canada approves new cancer immunotherapy treatment

A new cancer treatment recently approved in Canada promises to cut treatment time down to just minutes, but experts have differing opinions on whether it’s what’s best for patients.

One fears that it will unnecessarily use a higher dose of an existing drug and is likely to be pricier than the current method of administrating it intravenously.

By contrast, another oncologist says it is a welcome development that can drastically reduce the time for cancer treatment.

New cancer treatment in Canada

Health Canada approved the sale of Tecentriq SC last month, a prescription medication that treats patients with lung cancer, liver cancer and breast cancer in a new subcutaneous formulation of the already approved drug atezolizumab.

Atezolizumab is currently used in intravenous form as Tecentriq IV to treat various tumours. The new subcutaneous type of cancer immunotherapy treatment injects the drug under the skin instead of intravenously into the veins.

Mississauga, Ont.-based pharmaceutical company Roche Canada said in a news release last week that the Tecentriq subcutaneous injection helps to strengthen the immune system’s ability to fight cancerous cells. The company told that it’s the first cancer immunotherapy subcutaneous injection for multiple cancer types in Canada.

This treatment has been approved in more than 30 countries. Switzerland-based pharmaceutical giant F. Hoffmann-La Roche Ltd. is Roche Canada’s parent company.

New immunotherapy seen as time-saver  

In addition to boosting the immune system, another potential benefit to patients is the flexibility this new treatment offers.

Roche Canada said the Tecentriq subcutaneous injection must be administered by a qualified health-care professional, but this could be done outside of a hospital, in another facility or even at a patient’s home.

Sharlene Gill, president of the Canadian Association of Medical Oncologists, said in a video interview with the subcutaneous formulation would reduce the time to treat patients who typically receive immunotherapy for a long period.

Administering subcutaneous injection under the skin could be done faster, such as in about 15 minutes compared to about an hour through IV, she explained.

“I’m not sure I would call it a game-changer, but I would say that this really matters to people in terms of: it may not be a new medicine, but it’s a better way of being able to deliver a highly effective medicine,” said Gill, who is also a professor of medicine at the division of medical oncology at the University of British Columbia in Vancouver.

“Where it can be done and how quickly it can be done are probably the two big benefits … For patients living with cancer, time is their most precious commodity.”

It could also free up the system to deliver treatment to more patients in hospital and provide more equitable access to cancer care for patients who may not live in a big city or near a chemotherapy unit, she added.

‘Does not change outcomes’

While Gill spoke about the benefits to patients, Bishal Gyawali, a medical oncologist and oncology professor at Queen’s University in Kingston, Ont., said he has some concerns.

He said he doesn’t believe Tecentriq SC is drastically different from what is already available since it uses the same drug, atezolizumab, which currently exists in intravenous form. Gyawali is co-founder of a movement made up of medical professionals and patient advocates called Common Sense Oncology, which aims to promote a more patient-centred approach to oncology.

For certain cancers, other immunotherapy drugs have better quality evidence and are preferred over atezolizumab, he added.

“This (subcutaneous treatment) does not change outcomes, because it’s just a matter of convenience – intravenous injection versus subcutaneous injection,” Gyawali said in a video interview with “In terms of efficacy, it’s the same thing as an intravenous drug.”

Gyawali said he feels it’s not a big burden to take atezolizumab intravenously, as the drug is given once every four weeks. He said the evidence suggests an intravenous injection could even be given every eight weeks with the same effect.

‘What is the price of comfort?’

Based on the way atezolizumab has been tested in one clinical trial, Gyawali says Tecentriq SC will be sold and used at a higher dose of 1,875 milligrams. That’s equivalent to the IV dose of 1,200 mg in terms of achieving drug concentration in the blood, Gyawali said. However, he believes the 1,200 mg dose every three weeks is more than what is needed for “optimal efficacy.”

The study concluded that intravenous and subcutaneous treatments are equally effective. Its results were published in the Annals of Oncology in August 2023. F. Hoffmann-La Roche Ltd., the parent company of Roche Canada, funded the trial.

Gyawali said it’s a “missed opportunity” as the trial tested the higher dose despite evidence that a lower dose can be equally effective.

He said that the IV dose is already higher than what is needed for patients.

“There is no doubt about it but the industry is testing or recommending a higher dose than what is needed and not testing lower dose simply because with higher dose they can make more money,” Gyawali said.

What’s more, he said, he expects the new subcutaneous injection will cost “substantially more” than the intravenous version in part because he thinks it will be marketed as offering convenience.

“How much more are we willing to pay for a subcutaneous injection versus the same drug in the intravenous form that patients can get once every month?” he said. “What is the price of comfort, so to speak?”

In addition, he said he fears a potentially higher dosage of atezolizumab or any immunotherapy, regardless of formulation, could lead to more side effects, drug wastage and higher costs. He described a problem with what he said were unnecessarily higher doses involving other immunotherapy drugs such as pembrolizumab and nivolumab, as well.

A picture shows the logo of Swiss pharmaceutical giant Roche at its headquarters in Basel on February 17, 2015. AFP PHOTO / SEBASTIEN BOZON (Photo by SEBASTIEN BOZON / AFP) (Photo by SEBASTIEN BOZON/AFP via Getty Images)

Laura Pagnotta, spokesperson for Roche Canada, didn’t respond directly to about Gyawali’s accusations the company was mainly motivated by profit over patients’ best interests in testing higher doses that the oncologist believes are unnecessary for the treatment.

Instead, she said in an email to that Health Canada’s approval “signals the safe and effective use of the treatment, based on robust data.”

Regarding concerns about potential side effects from higher doses, Pagnotta said the clinical study found no serious safety concerns.

“The safety profile of the Tecentriq SC formulation is consistent with that of Tecentriq IV and the rate of adverse events (side effects) was similar in clinical trials,” Pagnotta said in an email. “No infusion-related reactions occurred in the study of Tecentriq SC and injection-site reactions were mild in nature, had no impact on administration, and were mostly resolved without additional treatment.”

Calling it “an important first step,” Pagnotta said the company can now have conversations with the pan-Canadian Pharmaceutical Alliance and the federal, provincial and territorial agencies to discuss “the price, the value of the innovation, and the data to support both.”

“We have a robust package to submit for review and look forward to the discussion and to bringing this treatment to patients as quickly as possible,” she wrote. “With a treatment like Tecentriq subcutaneous, we hope to not only ease the burden of treatment for patients, but also save some of the healthcare system costs associated with more labour-intensive and time-intensive treatments and formulations so that those resources can be diverted back into overall cancer study, prevention, and disease management across the system.”

While the new treatment reduces the complexity of delivering the drugs, Gill said it still has to be done by qualified professionals, and patients have to be monitored for side effects.

“I think these kinds of developments make incremental improvements in patients’ experience on their cancer journey and how they’re experiencing cancer,” Gill said. reached out to Health Canada for comment, but did not receive a response in time for publication.

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