The number of childhood cancer survivors in the U.S. has increased, but the majority of those who have survived five or more years after diagnosis face chronic health problems related to their treatment, according to a new Northwestern Medicine study in collaboration with the National Cancer Institute (NCI) and St. Jude Children’s Research Hospital.
The study is the first to estimate the prevalence of treatment-related chronic disease among survivors of childhood cancer at a national level. It found there are nearly 400,000 childhood cancer survivors in the U.S. as of 2011, up 60,000 from 2005.
“We’ve been able to increase the number of survivors of pediatric cancer, but simply curing their disease isn’t enough,” said lead author Dr. Siobhan Phillips, assistant professor in Preventive Medicine-Behavioral Medicine. “We need a more coordinated approach to their care to help prevent or delay some of these chronic health problems that affect the quality of their lives. We want them to thrive, not simply survive.”
The study was published April 1 in Cancer Epidemiology, Biomarkers & Prevention, a journal of the American Association for Cancer Research.
“The magnitude of diseases at relatively young ages is quite striking, since you would not expect many of these diseases to be a problem in the general population until much older ages,” said Dr. Phillips, also a faculty member at the Institute for Public Health and Medicine – Center for Population Health Sciences.
Among the health problems experienced by childhood cancer survivors are mental impairment, anxiety, pain and physical limitations that affect daily living.
About 70 percent of the survivors of childhood cancers were estimated to have a mild or moderate chronic condition, and about 32 percent were estimated to have a severe, disabling, or life-threatening chronic condition. An estimated 35 percent of the survivors, ages 20 to 49, had neurocognitive dysfunction; about 13 to 17 percent of those in this age group had self-reported functional impairment, activity limitations, impaired mental health, pain or anxiety/fear.
“These facts should challenge all of us in the field not to be content simply with improving lifespan, but to dedicate the future of this field to improving the ‘health span’ of our survivors,” said Dr. Greg Armstrong, principal investigator of the Childhood Cancer Survivor Study and a pediatrician at St. Jude.
“Several important research questions arise from these findings as we consider how to increase our understanding of the chronic and late effects of treatment and how to best develop guidelines and interventions to treat these chronic morbidities in this important population,” said co-author Dr. Lynne Padgett, rehabilitation psychologist and program director of the NCI at the National Institutes of Health (NIH).
Childhood cancer survivors should have health care providers who are knowledgeable about their increased risk of chronic health problems, Dr. Phillips said. Northwestern’s Lurie Cancer Center has a comprehensive long-term follow-up program for adult survivors of pediatric cancer. The STAR Program follows survivors through adulthood, focusing on their special medical and psychological needs.
For the study, the researchers used cancer incidence and survival data recorded between 1975 and 2011 from nine U.S. Surveillance, Epidemiology, and End Results registries, and data from the Childhood Cancer Survivor Study cohort that had information on a range of potential adverse and late effects of cancer treatment from more than 14,000 long-term survivors of childhood cancers at 26 cancer centers across the U. S. and Canada.
The Childhood Cancer Survivor Study is supported by grant U24-CA-55727 from the NCI of the NIH.
See journal article: http://cebp.aacrjournals.org/content/24/4/653.abstract