HEALTH CARE

Research paves the way to safer, more effective treatment for children with aggressive blood cancers

Australian nanomedicine researchers have come up with a new approach to solving a decades-old clinical problem: getting treatment drugs to act selectively on cancer cells in the body. Published this week in the high-impact journal Science Translational Medicine, the research paves the way to safer and more effective treatment options for children with aggressive blood cancers, and potentially other types of cancer as well.

Chemotherapy is the mainstay of treatment for leukemia, the most common blood cancer in children. However, while chemotherapy can be very effective for certain types of leukemia, it is not as effective for some other types, known as ‘high-risk’ leukemias. Treatment for high-risk leukemias generally involves high doses of toxic drugs that flood the body, indiscriminately affecting cancer cells and healthy cells alike. This often leads to severe side effects, as well as lifelong health issues in survivors.

Finding a way to make treatment drugs act more selectively on cancer cells is the key to improving treatment success while reducing toxicity in children treated for high-risk leukemia. By specifically targeting leukemia cells, we can make treatment more effective, as well as much safer to use in children.”


Professor Maria Kavallaris AM, Head of the Translational Cancer Nanomedicine theme at Children’s Cancer Institute

In the newly published research, scientists at Children’s Cancer Institute and collaborating organizations used a special formulation of the cancer drug, doxorubicin (Caelyx), in which the drug is encapsulated in tiny particles called liposomes. To this formulation, they added ‘bi-specific antibodies’ – antibodies capable of recognizing and attaching to the drug at one end and to cancer cells at the other end, effectively acting as a bridge between the two. Known as a ‘targeted drug delivery system’, this acts to deliver the drug to its target, in this case leukemia cells, where the drug can do its job and kill the cells.

“What is particularly useful about this new approach is its flexibility,” explained lead author, Dr Ernest Moles, Research Fellow at Children’s Cancer Institute. “We can use this system to target any leukemia, including the high-risk subtypes that are killing Australian children every year. Rather than having to design a completely new therapeutic each time, all we need do is change the antibody bridge, and we can target the same drug to any child’s blood cancer.”

“What’s more, this approach could allow us to counter drug resistance in an individual patient. If the cancer cells in a child try to evade chemotherapy by altering their cell surface, we can modify the targeted drug delivery system so it is able to recognize that altered cancer cell. There will be no easy escape.”

The new approach was shown to work well not only in leukemia cells grown in the laboratory, but also in living models of the disease. In these models, the targeted drug delivery system was found not only to reduce the amount of leukemia, but also to significantly prolong survival – in some cases, up to four-fold.

The researchers believe this same approach could be used to improve the selectivity of a whole range of new-generation therapeutic agents, not just chemotherapy drugs, opening the way to offering children alternative therapeutic options that are much safer than those currently on offer. They are also excited about the potential contribution it could make in the dawning era of precision medicine.

“In the future, it may be that each child diagnosed with leukemia can have their treatment targeted to their specific subtype, based on the analysis of a blood sample,” said Professor Kavallaris.

“We believe the controlled targeting of nanotherapeutics represents a real milestone in the treatment of childhood cancers, and we’re very optimistic about where this could lead to.”

Matt Weston and his son Jacob, who is currently being treated for acute lymphoblastic leukemia, know all too well the significance of this research. “I’ve followed this research project closely, and I’ve been absolutely blown away by the work of Maria, Ernest and the team at Children’s Cancer Institute,” said Matt.

“Having experienced firsthand how toxic the chemo treatment is through my son’s journey, I could tell you some horror stories of the side effects even with a standard risk diagnosis. For those with high-risk leukemia, not only is the treatment far more toxic, but their chances of survival are much lower as well.

“I think about those children and their families all the time, and to know that we are closer to improving the treatment, reducing the toxicity, and improving their chances of survival gives me great hope.”

Jacob has already been through several cycles of chemotherapy over the past eight months, and has experienced a range of debilitating side-effects. But it’s not over yet. He has another 16 months of maintenance therapy to go, then it will be another three years beyond that before he gets the all-clear. “It’s a long road ahead,” says Matt. You can read more about Jacob’s story here.

Several institutions collaborated on the research, including Children’s Cancer Institute, University of Queensland, University of NSW Sydney, University of Western Australia, Curtin University, Prince of Wales Hospital, St Vincent’s Hospital, Perth Children’s Hospital and Telethon Kids Institute. Key funding bodies included the National Health and Medical Research Council, Cancer Council NSW, and Tour de Cure.

Source:

Children’s Cancer Institute Australia

Journal reference:

Moles, E., et al. (2023) Targeted delivery of PEGylated liposomal doxorubicin by bispecific antibodies improves treatment of high-risk childhood leukemia. Science Translational Medicine. doi.org/10.1126/scitranslmed.abm1262.

Originally Posted Here

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