null New cancer screening tool may help childhood cancer survivors
A novel cancer predisposition screening tool shows promise in helping doctors better predict which childhood cancer survivors may be at risk of developing future cancers.
Source: MUHC. Researchers from The Hospital for Sick Children (SickKids) and the Montreal Children’s Hospital (MCH) and Research Institute of the McGill University Health Centre (RI‑MUHC) have shown that a screening tool used to identify genetic predisposition to cancer could also help predict which childhood cancer survivors may be at risk of developing other cancers later in life. The researchers say the findings could help clinicians consider more precise surveillance strategies for cancer survivors. The study was published in the Journal of Clinical Oncology in August 2021.
Cancer survivors have a higher risk for developing subsequent malignant neoplasms (SMN), tumours that result from genetic factors and exposure to cancer therapies such as radiation and chemotherapy.
Led by Drs. Paul Nathan from SickKids, Noelle Cullinan, former hematology/oncology fellow at SickKids and current Locum Consultant Paediatric Oncologist at Children's Health Ireland at Crumlin (Dublin, Ireland), and Catherine Goudie, MD, a Pediatric Hematologist-Oncologist at the MCH and Junior Scientist at the Research Institute of the McGill University Health Centre, the research team used an application called MIPOGG (McGill Interactive Pediatric OncoGenetic Guidelines). MIPOGG uses decisional algorithms to identify which patients may have a cancer predisposition syndrome – a genetic disease that can increase the likelihood of developing one or more cancers – and should undergo genetic evaluation to determine if they are indeed at higher risk.
In this study, the researchers used MIPOGG to assess whether the tool could help predict which cancer survivors are at risk of developing subsequent cancers. The team found that a MIPOGG recommendation for genetic evaluation was associated with an increased risk of developing an SMN, over and above the known risk factors of chemotherapy and radiation.
“If we are able to identify which childhood cancer survivors are more likely to develop subsequent cancers, we can create better surveillance strategies that are individualized to the specific therapies and cancers those individual patients have already experienced,” says Dr. Nathan, Senior Associate Scientist, Child Health Evaluative Sciences and Oncologist in the Division of Haematology/Oncology at SickKids. “These findings open up the door to a whole new precision approach to managing aftercare and surveillance for childhood cancer survivors.”
The population-based study, made possible by the POGONIS registry (POGO), reviewed records from 1,886 cancer patients diagnosed with a childhood cancer in Ontario between 1986 to 2015, including 317 cases in which the patient had developed an SMN. The team found that SMN prediction by the tool was higher for certain cancer types and in survivors who had not previously received radiation therapy.
“To our knowledge, this is the first validated decision-support eHealth tool to predict second cancers in paediatric oncology patients. This could change the survivorship journey for many patients and families and help prioritize patients for genetic evaluation, especially in settings with lower access to genetic testing,” says Dr. Goudie, who is a member of the Child Health and Human Development Program at the RI-MUHC’s Centre for Outcomes Research and Evaluation.
The study team notes the next steps for this research are to evaluate the cost-effectiveness of the tool in supporting cancer predisposition syndrome screening.
“SickKids has been championing a new approach to paediatric medicine called Precision Child Health (PCH). Finding tools to support clinical decision-making that can help lead to earlier diagnosis for cancer survivors is one way we can achieve that vision,” says Nathan, who is also the Director of the AfterCare Program and Head of the Solid Tumour Section in Haematology/Oncology at SickKids.
Funding for the study was provided by the Cancer Research Society, Montreal Children’s Hospital Foundation, Cedars Cancer Foundation/Sarah's Funds for Cedars, Pediatric Oncology Group of Ontario (POGO) and SickKids Foundation.
About McGill Interactive Pediatric OncoGenetic Guidelines (MIPOGG)
MIPOGG is an app that identifies children at higher risk of cancer predisposition syndromes in pediatric oncology. These syndromes are recognized as an important cause of pediatric cancer development. Health professionals who manage children and adolescents with cancer have a unique opportunity to identify these patients and their families for genetic evaluation. This task is increasingly challenging for clinicians as the knowledge of cancer genetics is growing at a rapid pace. Conceptualized by Dr. Catherine Goudie and further developed via the collaboration of the Montreal Children’s Hospital of the McGill University Health Centre and The Hospital for Sick Children (SickKids), with the support of numerous partners, MIPOGG offers access to simple tumor-specific algorithms that guide the clinician through the decisional process of whether a child requires a genetics referral. MIPOGG incorporates evidence-based educational modules outlining associations between pediatric tumors and cancer predisposition syndromes. mipogg.com
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