Representational Image.
Washington, Oct 8: With an overall survival rate of more than 85% five years after diagnosis, the number of children cancer survivors in the United States is rising. However, survivors may still be more susceptible to a number of illnesses, such as second cancers.
Researchers at St. Jude Children’s Research Hospital found a genetic explanation for why a small percentage of survivors are more likely to develop second cancers, which may be more severe or fatal, using data from the Childhood Cancer Survivor Study (CCSS) and the St. Jude Lifetime Cohort Study (St Jude Life).
The findings, which will help with genetic counselling, testing, and the implementation of personalised cancer screening and preventive programmes, were published in The Lancet Oncology.
The St Jude group showed that survivors with pathogenic (damaging) genetic variants in specific genes, called cancer-predisposing variants, are at an increased risk of developing second, or subsequent, cancers as adults, and those cancers are more likely to be severe and deadly.
The scientists had previously identified that survivors with pathogenic variants in one of 60 different cancer-predisposing genes or 127 DNA damage repair genes were more likely to experience a second or subsequent cancer. This study extends that research to show a direct connection between cancer-predisposing variants and increased second-cancer-related mortality.
Many of these genetic variants are known to be causally linked to cancers. For example, the tumor suppressor gene TP53 is one of the 60 genes included in the analysis.
The key to the discovery’s utility is that these variants are present in the DNA of patients when diagnosed with cancer as children, allowing for an individualized medicine approach to be developed early in life for each survivor.
By better understanding the effect such genes can have on future cancer risk and its outcome beyond primary childhood cancer, the study will help inform efforts to prevent second cancers and improve the outcomes in these individuals.
“Our study pinpoints that clinical genetic testing to screen for and identify if survivors are carriers of these pathogenic variants could lead to screening and early interventions for those at higher risk to develop deadly second cancers, potentially saving their lives,” said senior corresponding author Zhaoming Wang, PhD, St. Jude Department of Epidemiology and Cancer Control.
The total number of childhood cancer survivors who develop second or subsequent cancers is small , and the percentage of survivors who carry cancer-predisposing variants is low (~6 per cent).
Together, these factors have made it extremely challenging to study and understand the genetic risks for second cancers and their outcome in this population. To reach statistically meaningful results, Wang and his collaborators combined whole genome/exome sequencing and clinical data from over twelve thousand survivors of childhood cancer.
The study combined data from North America’s two largest survivorship studies, the CCSS and St Jude LIFE cohorts.
“This is the first comprehensive study looking for the genetic reason for late mortality — specifically late mortality due to second cancers,” Wang said. “Now we know that cancer-predisposing variants contribute to the risk of death from second cancer.” Increased surveillance may help limit the impact of these cancer-predisposing variants as childhood cancer survivors grow into adulthood. By knowing which survivors are at greater risk, healthcare providers may be able to recommend personalized cancer screening, which may lead to the detection of additional cancers at their earliest and most treatable stage.
These variants are part of the inherited, or germline, DNA that people are born with. This means they can be detected in children when they are first diagnosed with childhood cancers, arming survivors with the knowledge they need to lower their risk later in life.
